Identification of a pro-angiogenic functional role for FSP1-positive fibroblast subtype in wound healing

Saraswati, Sarika; Marrow, Stephanie M. W.; Watch, Lester A.; Young, Pampee P.

doi:10.1038/s41467-019-10965-9

Download PDF

Article
Open access
Published: 09 July 2019

Identification of a pro-angiogenic functional role for FSP1-positive fibroblast subtype in wound healing

Sarika Saraswati ORCID: orcid.org/0000-0002-5674-8371¹,
Stephanie M. W. Marrow¹,
Lester A. Watch¹ &
…
Pampee P. Young^1,2

Nature Communications volume 10, Article number: 3027 (2019) Cite this article

7836 Accesses
50 Citations
21 Altmetric
Metrics details

Subjects

Abstract

Fibrosis accompanying wound healing can drive the failure of many different organs. Activated fibroblasts are the principal determinants of post-injury pathological fibrosis along with physiological repair, making them a difficult therapeutic target. Although activated fibroblasts are phenotypically heterogeneous, they are not recognized as distinct functional entities. Using mice that express GFP under the FSP1 or αSMA promoter, we characterized two non-overlapping fibroblast subtypes from mouse hearts after myocardial infarction. Here, we report the identification of FSP1-GFP⁺ cells as a non-pericyte, non-hematopoietic fibroblast subpopulation with a predominant pro-angiogenic role, characterized by in vitro phenotypic/cellular/ultrastructural studies and in vivo granulation tissue formation assays combined with transcriptomics and proteomics. This work identifies a fibroblast subtype that is functionally distinct from the pro-fibrotic αSMA-expressing myofibroblast subtype. Our study has the potential to shift our focus towards viewing fibroblasts as molecularly and functionally heterogeneous and provides a paradigm to approach treatment for organ fibrosis.

SenNet recommendations for detecting senescent cells in different tissues

Article 03 June 2024

Acquisition of epithelial plasticity in human chronic liver disease

Article Open access 22 May 2024

Tumor-associated macrophages restrict CD8+ T cell function through collagen deposition and metabolic reprogramming of the breast cancer microenvironment

Article 03 June 2024

Introduction

Fibrosis is the typical response to injury that leads to distorted tissue architecture, pathologic signaling and ultimately organ dysfunction¹. In response to tissue injury, a population of fibroblasts activates, proliferates, and plays a vital part in the entire repair process: from the generation of granulation tissue, revascularization and restoration of cardiac architecture, and function to tissue remodeling and eventually scar formation². Reduced fibroblast function may lead to ventricular dilatation and catastrophic rupture due to failure to repair the infarcted region^2,3. Alternatively, continued and unchecked fibroblast activity results in fibrosis, adverse cardiac remodeling, and ultimately heart failure⁴.

It is increasingly recognized that fibroblasts are a phenotypically and functionally diverse population of cells that must be studied in a temporal and tissue/injury-specific context^5,6,7. In an uninjured heart, for example, fibroblasts are quiescent and express surface markers such as vimentin, Tcf21, and PDGFRα⁸. Following injury, resident fibroblast populations expand and express proteins unique to their activated state^2,9. Two markers expressed in the post-injury (activated) fibroblasts are fibroblast specific protein 1 (FSP1; S100A4) and α smooth muscle actin (αSMA); however, neither marker is exclusively specific to fibroblasts^10,11,12,13. These markers are absent in the quiescent fibroblasts of heart, kidney, and lung^11,12,14. αSMA protein, expressed in myofibroblasts, has long been studied as a hallmark of pathological fibrosis. Less is known about the significance of FSP1, a member of the S100 family of intracellular calcium-binding proteins. Several studies have confirmed FSP1 as a marker of injury-induced fibroblasts^12,13,15. Interestingly, FSP1⁺ and αSMA⁺ fibroblasts have been reported to be non-overlapping fibroblast populations in the injured heart, skin, liver, and kidney^{5,6,11,12,13,16}, but their population dynamics as well as their functional and molecular differences in the context of tissue repair are lacking.

We hypothesize that functional and molecular characterization of the major post-injury fibroblast subtypes is necessary to target the pathological scarring/fibrotic effects of fibroblasts without impeding their pro-reparative functions. In this study, we used transgenic mice in which FSP1 and αSMA-expressing cell populations were genetically tagged with GFP. We isolated these fibroblast subpopulations from the injured murine heart, taking specific care to exclude non-fibroblast populations, which are also known to express the FSP1 protein. Detailed molecular and functional studies are done to identify the unique roles of FSP1 and αSMA-expressing fibroblasts in injury repair.

Results

FSP1 and αSMA are present in distinct cells post injury

We evaluated the expression pattern of FSP1 and αSMA proteins in uninjured organs and at various time points following tissue injury. For cardiac injury (Fig. 1a), myocardial infarctions (MIs) were induced by ligation of the left anterior descending coronary artery (LAD) in mice¹⁷. Human cardiac tissue was collected postmortem from cadavers at least 2 weeks post infarct (Fig. 1d). For skin injury, excisional (1 cm) full-thickness wounds (Fig. 1b) were generated on the dorsum¹⁸. Kidney injury (Fig. 1c) was induced by unilateral ureteral obstruction by ligating the ureter just distal to the renal pelvis¹⁹. FSP1 and αSMA protein expression and localization with respect to injury were evaluated by co-immunofluorescence (IF) using confocal microscopy. Consistent with published studies, uninjured heart, skin, and kidney tissues were negative for anti-FSP1 staining^11,12,13. Anti-αSMA staining in uninjured and at early time points after injury was restricted to vascular structures (such as pericytes and vascular smooth muscle cells). FSP1⁺ stromal cells were detectable within 48 h of injury in heart, at day 4 in skin, and at day 7 in the injured kidney parenchyma, whereas significant αSMA expression (excluding perivascular cells) appeared between 7 and 8 days after injury in all three models. In the cardiac infarct model the abundance of cells expressing both markers declined significantly (or were completely absent) by day 30 after the generation of stable scar. No co-localization or overlap between these two cell populations was identified in the heart, kidney, or skin at any post-injury time point evaluated. FSP1 has been noted by multiple groups to also mark hematopoietic (myeloid) cells^10,16 and endothelial cells⁸. We confirmed that a population of both hematopoietic and endothelial cells expressing FSP1 were present in injured mouse left ventricles (LV) at post-MI d8 (Supplementary Fig. 1A). However, around 15% of the GFP⁺/FSP1⁺ cell population did not stain with CD45 or CD31 as identified through flow cytometry analysis and confocal microscopy, indicating the presence of a non-hematopoietic and non-endothelial FSP1-expressing cell subset (Supplementary Fig. 1, A, B).

To further study the degree to which FSP1⁺ cells originated from the bone marrow, FSP1-GFP chimeric mice were generated that had undergone ablative bone marrow transplantation (BMT) from syngeneic C57BL/6 mice. The FSP1-GFP reporter mice (gift from Dr. Eric Neilson) express GFP under the FSP1 promoter. However, the FSP1-GFP chimeric animals, following engraftment with C57BL/6 marrow, would cease to express GFP from any bone marrow-derived cells. These chimeric animals enabled us to evaluate the degree to which the number of GFP⁺ cells present in the injured site were the result of inflammatory cells migrating into the injury site from circulation. As expected, there was a significant reduction in GFP⁺ hematopoietic cells in the injured myocardium as identified by CD45 expression alone (from 42.9 to 2.4%) or by CD45/CD31 co-staining (from 34.8 to 7.75%) in BMT GFP-FSP1 mice in comparison to non-BMT GFP-FSP1 mice (Supplementary Fig. 2). These results indicated that a substantial number of GFP-expressing FSP1⁺ cells in the injured heart were indeed hematopoietic cells originated from bone marrow. After exclusion of the BM-derived FSP1⁺ population, we observed a relative increase in non-hematopoietic GFP⁺/FSP1⁺ cells, lacking hematopoietic markers from 14.7 to 65.8% in BMT GFP-FSP1 chimeric mice, demonstrating that a majority of the FSP1⁺ fibroblasts originated at the site of injury (Supplementary Fig. 2). These data confirmed that the injured heart contained substantial numbers of both FSP1⁺ fibroblasts and non-fibroblasts (hematopoietic and endothelial cells) post injury. In addition, most of the non-hematopoietic cells originate at the site of injury and are not recruited from the bone marrow.

FSP1⁺ and αSMA⁺ fibroblast isolation from the injured heart

Our data above support published reports that FSP1⁺ and αSMA⁺ cells are indeed unique post-injury fibroblast populations^{5,6,11,12,13,16}. Little is known about the physiologic characteristics and cellular roles of these two subsets. To identify the cellular, molecular, genomic, and functional features of these fibroblast subtypes, we isolated FSP1 and αSMA-expressing cells from two distinct reporter mice that express GFP under FSP1 (FSP1-GFP) or αSMA (αSMA-GFP) promoters (gifts from Drs. Eric Neilson and Ivo Kalajzic, respectively) from left ventricle of mice post infarct^20,21. Since we observed peak endogenous expression of FSP1 and αSMA protein between day 8 and 15 after experimental MI (Fig. 1a), we selected that time frame post MI (i.e., d10 post MI) to isolate each respective post-injury GFP⁺ fibroblast cell type by fluorescence assisted cell sorting (FACS) (Fig. 2a). To better understand the reporter fidelity of the αSMA mouse model, we evaluated the percentage of GFP⁺ cells which co-expressed αSMA and found that to be very high at both 4 and 10 days after MI (88% ± 0.7 standard deviation (SD) and 99.9% ± 0.05 SD, respectively, n = 3 for uninjured, d4 and d10 post MI, Supplementary Fig. 3). Interestingly, the percentage of αSMA + cells which were GFP + was less at day 4 (19.5% ± 0.6 SD) and rose to 94% ± 7 SD at day 10 (Supplementary Fig. 3), suggesting that GFP expression lagged somewhat behind αSMA expression. Importantly, during the time frame of d10 post MI used for αSMA cell isolation, there was high concordance of αSMA cells which expressed GFP and vice versa. As expected, negligible number of cells were positive for GFP and αSMA co-staining in uninjured heart (Supplementary Fig. 3). The expression pattern of FSP1 and GFP protein in GFP-FSP1 mice has been well characterized elsewhere^10,20.

Since the uninjured hearts had no detectable GFP⁺ cells in both murine models, these cells isolated from uninjured mice were used to establish the background signal in the GFP channel post compensation for all experiments (Fig. 2b). A gate was drawn to capture all cells producing a larger voltage pulse area than the established background in the GFP channel. Both FSP1⁺ and αSMA⁺ cells were sorted based on GFP expression. To eliminate contaminating FSP1⁺ hematopoietic and endothelial cells, CD45 (GFP⁺; 12–16%) and CD31 (GFP⁺; 8–15%) cells were excluded during our sorting for FSP1⁺ fibroblasts (GFP⁺/CD45⁻/CD31⁻; 10–20%)⁸ (Fig. 2c, Supplementary Figs. 5 and 6B, and Supplementary Table 4). A negligible amount of endothelial (GFP + /CD31 + cells; 3.8% ± 0.0164 SD; n = 5) and hematopoietic (GFP + /CD45 + cells; 3.18% ± 0.0112 SD; n = 5) cells co-express GFP in injured αSMA-GFP mouse hearts and were not excluded during GFP sorting (GFP⁺, 15–20%) from αSMA-GFP mouse hearts (Fig. 2b, Supplementary Figs. 4 and 6A, and Supplementary Table 3). Further immunostaining of the sorted populations of both FSP1 and αSMA ensured that CD45 and CD31 cells were absent from both fibroblast isolations (Fig. 2d). Although, we took substantial measure to ensure cellular purity of FSP1 and αSMA cell population, we cannot rule out the caveats of using transgenic mouse models to isolate cell types based on transgene expression. The isolation may contain rare, contaminating cells that do not represent fibroblasts. Following sorting, our first step was to confirm the identity of GFP-expressing FSP1⁺ and αSMA⁺ cells as fibroblasts. FACS sorted cells were plated on coverslips and confirmed by IF to express FSP1 antigen and to lack expression of αSMA as well as hematopoietic and endothelial markers, CD45 and CD31 (Fig. 2d). GFP⁺/CD45⁺ or GFP⁺/CD31⁺ cell populations were used as positive controls (Supplementary Fig. 7). To support our observations from histologic immunolocalization in injured tissues, FACS sorted GFP⁺ cells (Fig. 2b, c) from the injured heart of αSMA-GFP and FSP1-GFP reporter mice were negative for FSP1 antigen or αSMA antigen, respectively, but exhibited robust expression of their respective proteins, αSMA, or FSP1 (Fig. 2d). Both FSP1⁺ and αSMA⁺ cells expressed Collagen type 1 alpha-1 chain (COL1α1), periostin, and vimentin by IF analysis. On the other hand, uninjured fibroblasts expressed vimentin but lacked expression of activated fibroblast markers: FSP1, αSMA, periostin, and COL1α1. Ultrastructural evaluation of fibroblast subtypes showed abundance of rough endoplasmic reticulum, golgi apparatus, and mitochondria with elongated nucleus in αSMA⁺, FSP1⁺, as well as uninjured fibroblast subtypes as described earlier for fibroblasts and myofibroblasts (Supplementary Fig. 8A)²². Primary mouse microvascular endothelial cells, used as a control, appeared quite distinct from the fibroblast subtypes with dense cytoplasm and fewer numbers of intracellular organelles. Moreover, around 95–97% of all three fibroblast subtypes stained positive for fibroblast marker MEF-SK4 by flow cytometry (Fig. 2e)²³ and expressed transcripts of fibroblast specific markers Pdgfrα, Col3, Col1α1, and Fn1 as assessed by semiquantitative real-time PCR (Supplementary Fig. 8B). Also, none of the three fibroblast subtypes expressed the pericyte marker, AN2 (a mouse homolog of the rat NG2), determined by semiquantitative real-time PCR and flow analysis (Fig. 3a, b, Supplementary Figs. 4 and 5, Supplementary Tables 3 and 4). In fact, confocal analysis of injured human heart failed to indicate any co-localization between FSP1 and AN2/NG2 (Fig. 3c). Interstitial as well as perivascular location of AN2-positive cells was evident in the injured heart, whereas FSP1⁺ fibroblasts were primarily localized in the interstitial space. These results determined that isolated fibroblast subtypes, specifically the less characterized FSP1⁺ subtype, are distinct from injury-activated pericytes. Importantly, FSP1⁺ (GFP⁺/CD45^–/CD31⁻) fibroblasts exhibited similar levels of collagen gel contractility and proliferative activity (Fig. 2f) as shown by both uninjured fibroblasts and αSMA⁺ fibroblasts. These results demonstrated successful isolation of activated FSP1⁺ (GFP⁺/CD45⁻/CD31⁻) and αSMA⁺ fibroblasts from injured hearts using two distinct reporter mice. Their identity as fibroblasts was confirmed by molecular, ultrastructural, phenotypic, and functional characterization.

FSP1⁺ fibroblasts do not differentiate into αSMA fibroblasts

Our data demonstrated no cellular co-localization between FSP1 and αSMA-expressing cells in three different tissue injury models. Since many studies have demonstrated undifferentiated fibroblasts to differentiate into αSMA-expressing myofibroblasts in defined medium, we assessed if FSP1-expressing fibroblasts could be similarly induced^24,25. We cultured FSP1-expressing as well as uninjured fibroblasts in the presence of TGFβ in conditions previously published as permissive for myofibroblast differentiation²⁴. As expected, primary fibroblasts from uninjured hearts differentiated into αSMA-expressing myofibroblasts identified by immunofluorescence (Fig. 4a) and semiquantitative real-time PCR analysis (Fig. 4b) whereas FSP1-expressing fibroblasts failed to differentiate into myofibroblasts in vitro. αSMA-expressing fibroblasts were used as a positive control. These results further confirmed that FSP1 and αSMA-expressing fibroblasts were two distinct activated fibroblast subtypes, which did not change phenotype.

FSP1⁺ and αSMA⁺ fibroblasts are transcriptionally distinct

To identify the transcriptomic signature variability between these cell types, we employed a semiquantitative real-time PCR-based fibrosis array (Fig. 5a). Following the analysis of 84-gene panel PCR array, we identified distinct molecular signatures between αSMA⁺, FSP1⁺, and uninjured fibroblasts. Genes involved in matrix synthesis were upregulated in both FSP1⁺ and αSMA⁺ fibroblasts; although the level of these genes was much higher in αSMA⁺ vs. FSP1⁺ fibroblasts (Fig. 5b). Interestingly, Gremlin1 (Grem1) which is known to modulate angiogenesis was significantly elevated (4.75 fold) in FSP1⁺ in comparison with αSMA⁺ fibroblasts (Fig. 5c). The transcript levels of matrix metalloproteases 2 and 13 (Mmp2 and Mmp13) and pro-angiogenic factor Vegf were also modestly elevated in FSP1⁺ fibroblasts vs. αSMA⁺ fibroblasts. In addition, an array of transcripts including pro-fibrotic cytokines were significantly downregulated in FSP1⁺ vs. αSMA⁺ fibroblasts. The list includes interleukin 1 beta (IL1β; −18.14 fold), C-C chemokine receptor type 2 (Ccr2; −14.89 fold), C-X-C chemokine receptor type 4 (Cxcr4; −12.74 fold), Chemokine (C-C motif) ligand 3 (Ccl3; −7.81 fold), chemokine (C-C motif) ligand 12 (Ccl12; −6.8 fold), and tumor necrosis factor (Tnf; −3.26 fold) (Fig. 5d). The fibrosis array results were confirmed by RNA-seq and distinct molecular signatures of all three fibroblast subtypes were identified (Fig. 5e). KEGG pathway grouping on the DAVID bioinformatics Resource 6.7 platform identified that the fibrillary collagen genes (Col1a1, Col1a2, Col3a1) and the constituents of the TGFβ signaling pathway were highly upregulated in αSMA⁺ fibroblasts as compared with FSP1⁺ fibroblasts, suggesting a distinct role of the αSMA⁺ population in injury-initiated fibrosis. By contrast, genes known to have a positive impact on angiogenesis (such as Grem1, Il6, Il6r, Il10, and Il10r), MMPs, and genes involved in adhesion and migration (cadherin 5 and 13, integrin α2, α6, and β2) were much more highly expressed in FSP1⁺ vs. αSMA⁺ fibroblasts (Fig. 5f). Cell metabolism, cell cycle, and RNA biogenesis pathways were not significantly changed between the groups and are not reported here. Two independent transcriptomic analyses of freshly sorted fibroblast subtypes suggested that FSP1⁺ fibroblasts contributed to a regulatory and pro-angiogenic role whereas αSMA⁺ fibroblasts were drivers of matrix synthesis and scar formation following injury.

FSP1⁺ and αSMA⁺ fibroblasts respond to pro-fibrotic factors

In response to injury, there is an activation of several growth factor and cytokine signaling, including WNT and TGFβ. Similar levels of TGFβ signaling pathway activation were identified in both αSMA⁺ and FSP1⁺ fibroblasts, assessed through SMAD2 phosphorylation (Supplementary Fig. 9). Both FSP1⁺ and αSMA⁺ fibroblasts responded to WNT3A treatment as assessed by pLRP6 immunoblot. However, the response was much more robust in αSMA⁺ vs. FSP1⁺ fibroblasts. In addition, COL1α1 protein levels were slightly higher in αSMA⁺ fibroblasts than FSP1⁺ fibroblasts in response to WNT3A treatment. These results suggested that these two populations exhibit distinct activation thresholds to common post-injury modulators.

FSP1 expression is significantly induced by FGF2

αSMA and FSP1 proteins are expressed in injury-induced fibroblasts. Although TGFβ has been a well-documented growth factor which induces αSMA expression in fibroblasts²⁶, little is known about the injury mediated triggers that induce FSP1 expression. We tested the effect of multiple growth factors such as TGFβ, WNT3A, PDGF, and FGF2 on their ability to induce FSP1 transcript expression in uninjured fibroblasts by semiquantitative real-time PCR. These growth factors are involved in the multifaceted process of wound repair following injury^3,27,28,29. Even though in the presence of WNT3A and PDGF there was a modest increase in FSP1 expression, a significant increase in FSP1 expression was identified only in the presence of FGF2 (Supplementary Fig. 10). Previous reports have identified WNT3A as a trigger for FSP1 expression³⁰; however, our data suggest that FGF2 might be an important inducer for FSP1 expression in fibroblasts in the wound microenvironment. Regardless, these identifications do not rule out the complex interplay of multiple signaling cascades in regulating FSP1 expression in fibroblasts.

FSP1⁺ fibroblasts exhibit a pro-angiogenic protein signature

To validate the relatively higher pro-angiogenic transcriptional signature of FSP1⁺ fibroblasts, we used a multiplex panel of mouse angiogenesis proteome profiler antibody array (R & D) to measure 53 angiogenic analytes from FSP1⁺ vs. αSMA⁺ fibroblast lysates. Significantly increased expression of 14 out of 53 angiogenesis-related proteins were identified in FSP1⁺ fibroblasts including SDF1, CXCL16, Endoglin, Endothelin1, ADAMTS1, IGFBP-2 and -3, PDGF-AA, MMP-3, and Pentraxin-3 (Fig. 6a, Supplementary Fig. 11, and Supplementary Table 1). In contrast, only four angiogenesis-related proteins (DPPIV, osteopontin, serpin E1, and IP-10) were significantly upregulated in αSMA⁺ fibroblasts compared with FSP1⁺ fibroblasts (Fig. 6b, Supplementary Fig 11, and Supplementary Table 1). Several additional angiogenesis-related proteins exhibited a trend towards higher expression in FSP1⁺ vs. αSMA⁺ fibroblasts including VEGF, although the differences were not statistically significant. However, elevated expression of VEGF and GREM1 in FSP1⁺ fibroblasts were confirmed by an independent ELISA, which demonstrated significantly higher levels of secreted VEGF and GREM1 protein in conditioned media obtained from FSP1⁺ fibroblasts compared with αSMA⁺ fibroblasts (Fig. 6c). Moreover, elevated levels of GREM1 protein were also present in cell lysates of FSP1⁺ vs. SMA⁺ fibroblasts (Fig. 6c). In addition to Grem1, other pro-angiogenic genes such as Vegfa, Vegfb, Angpt1, and Fgf1 were significantly elevated in FSP1 fibroblasts in comparison with uninjured and αSMA fibroblasts by semiquantitative real-time PCR (Fig. 6d). Altogether, these data indicated a much robust pro-angiogenic phenotype of FSP1⁺ fibroblasts as compared with αSMA⁺ fibroblasts.

FSP1⁺ fibroblasts secretome is pro-angiogenic in vitro

The pro-angiogenic gene and protein signature prompted us to assess the effect of FSP1⁺ fibroblast conditioned media (CM) on promoting human umbilical vein endothelial cells (HUVEC) proliferation measured by BrdU incorporation (Fig. 7c) as well as HUVECs assembly (Fig. 7a, b) into interconnected tube like structures on a growth factor reduced matrix (vascular assembly). Both assays are commonly used to demonstrate pro-angiogenic effects. FSP1⁺ fibroblast CM significantly increased HUVEC proliferation (~1.7 fold; p < 0.0001) and vascular assembly in HUVECs (137.3 vs. 53.88 branch points/field of view; p = 0.0005) compared with no treatment. HUVECs treated with complete endothelial cell growth media (Lonza) were used as positive control. Interestingly, FSP1 protein also increased HUVEC proliferation (~1.34 fold; p = 0.0005) and vascular assembly (89.14 vs. 53.88 branch points/field of view; p = 0.0005) compared with no treatment, albeit not at the same extent as induced by FSP1⁺ fibroblast CM. The CM generated from the uninjured fibroblasts and αSMA⁺ fibroblast had marginal effect on HUVEC proliferation (Fig. 7f) and vascular assembly (Fig. 7a, b). These results suggested an angiogenesis promoting phenotype of FSP1-expressing fibroblasts which could be partly attributed to FSP1 protein, as previously reported^31,32.

FSP1⁺ fibroblasts are pro-angiogenic in vivo

To test if FSP1⁺ fibroblasts serve as a superior pro-angiogenic subpopulation in vivo, we implanted polyvinyl alcohol (PVA) sponges containing distinct fibroblast subtypes to study the granulation tissue formation. Implantation of PVA sponge discs is a well-established model used to study granulation tissue formation in vivo³³. Sponges were preloaded with freshly isolated and sorted FSP1⁺ (CD45⁻/CD31^–) or αSMA⁺ cardiac fibroblasts prior to their subcutaneous implantation beneath the ventral panniculus carnosus in adult mice. The mice were sacrificed on day 14, a time point in which the majority of the granulation tissue is generated by implanted fibroblasts, not by infiltrating host fibroblasts. Sponges were fixed with formalin and embedded for histological analysis to quantify the amount and quality of granulation tissue, vascularity (anti-CD31), and matrix deposition (Masson’s trichrome). Although we did not identify any statistically significant difference between the quality or extent of granulation tissue deposition, there was a striking increase in the percentage of CD31 stained vessels in sponges loaded with FSP1⁺ fibroblasts (6.817% ± 0.5496 SD; p < 0.0001) compared with αSMA⁺ fibroblast loaded sponges (1.78% ± 0.2463 SD; Fig. 7d, e). Notably, FSP1⁺ and αSMA⁺ fibroblasts, sorted for implantation, stained negative for endothelial cell markers (VWF and FLK-1), suggesting that the increased vasculature in FSP1⁺ fibroblast loaded sponges was host derived, and not derived from implanted FSP1⁺ or αSMA⁺ cells (Fig. 7g). These data have identified a significantly greater pro-angiogenic reparative role of FSP1⁺ than αSMA⁺ fibroblasts during cardiac healing following injury both in vitro and in vivo.

Discussion

Fibroblasts are recognized as a heterogeneous population of cells in several organ injury models^5,6,34,35,36. Recently, high-throughput single cell transcriptomic studies have identified several fibroblast subtypes in murine kidney and heart as well as in human skin tissues^37,38,39. However, a critical gap exists between recognizing the heterogeneity of fibroblast subtypes and identifying/understanding their functional differences and distinct roles on healing and fibrosis⁷. In fact, fibroblasts have been frequently studied as a homogenous entity when considering their functional roles in the injured heart as well as in other tissues^2,40,41. Though in uninjured organs, Thy1⁺ and Thy1⁻ fibroblast subtypes have designated functional roles which includes differences in their ability to form focal adhesions, cytoskeletal organization and migration⁴², in addition to differential expression of MHC class-II and CD40 expression, cyclooxygenase localization, and cytokine and prostaglandin production^35,43. Thy1⁺ and Thy1⁻ fibroblasts have been identified in injured (fibrotic) lungs⁴⁴; albeit without further functional characterization. Recently, bulk and single cell transcriptomics were utilized to predict the function of heterogeneous synovial fibroblast subtypes isolated from human rheumatoid arthritis patients⁴⁵. Based on functional assessment, a potentially pathogenic CD34⁻/Thy1⁺ fibroblast subtype was identified in vitro, the role of which needs to be assessed in vivo.

Our goal in the present study is to delineate the functional role of injury-induced activated two fibroblast subtypes in vitro as well as in vivo in order to better understand, target and mitigate fibrosis. Since post-injury-activated fibroblasts are both mediators of fibrosis and repair^2,3, understanding the functional differences in subpopulations may enable us to modulate detrimental fibrosis more precisely. The use of αSMA-GFP and FSP1-GFP mouse models have enabled us to FACS sort highly purified populations of distinct fibroblast subtypes, while carefully eliminating contaminating myeloid cells by gating where appropriate (i.e., FSP1-GFP). Subsequent immunophenotyping confirmed the absence of contaminating myeloid/hematopoietic and endothelial cell types from our isolated populations of both FSP1 and αSMA fibroblasts. We noted that one limitation of the αSMA-GFP model was that the transgene expression lagged behind the αSMA protein expression following MI, achieving a high degree of concordance (> 90%) at day 10 post injury. As a consequence, we used day 10 post MI for isolating αSMA fibroblasts.

While FSP1⁺ and αSMA⁺ fibroblasts have been reported as distinct fibroblast populations in injured tissues^11,12,13 and cancer¹⁵, no reports to date have elucidated their functional and molecular differences. In this study we have comprehensively evaluated these phenotypes both temporally and in multiple mouse models of tissue injury and in human infarcts. We have confirmed prior studies that FSP1⁺ and αSMA⁺ fibroblast subtypes are indeed distinct populations but also demonstrated that they appeared at different times following injury. FSP1-expressing fibroblasts were present at the wound site earlier than αSMA-expressing cells in three different injury models. We have identified that the FSP1-expressing fibroblast subtype has a predominant role in promoting angiogenesis post injury via multiple approaches, including transcriptomic, phenotypic, molecular, and functional analysis.

The dynamic process of wound healing requires several continuous and overlapping phases which includes an early phase of cellular homeostasis, cell recruitment, and vascularization, and a later phase of re-epithelization and collagen deposition⁴⁶. Fibroblasts, inclusive of all subtypes, have been implicated in immune cell recruitment and vessel formation as well as in collagen deposition and scar formation in both early and late wound healing^2,40,41,47. However, discrete roles of particular subtypes in regulating these overlapping processes have not been delineated. αSMA myofibroblast activation during the later phase of wound healing has been linked to wound contraction and scar formation to accelerate their progression⁴⁰. Onset of FSP1⁺ fibroblasts during the early phase of wound healing is suggestive of their contribution to immune cell recruitment, cellular proliferation and angiogenesis. Indeed, our transcriptomic data identified the elevation of chemo-attractants and chemokines such as IL-10 and IL-6, as well as MMP-3 and MMP-13 in FSP1⁺ fibroblasts compared with αSMA⁺ fibroblasts. In addition to being involved in injury-induced leukocyte infiltration, the aforementioned cytokines and MMPs have also been implicated in fostering regenerative wound repair and angiogenesis^48,49,50,51. Many landmark studies have shown that macrophages are critical players of wound healing and that they do so at least in part by promoting angiogenesis and collagen matrix deposition⁵². Significant work has been done to understand the crosstalk between activated fibroblasts and macrophages during wound repair⁵³. However, the role of a specific fibroblast subtype in modulating the early phase of wound healing, which involves immune cell recruitment, has not been explored. Our identification of a sorted FSP1⁺ fibroblast population with a specific gene signature suggests their involvement in leukocyte recruitment, angiogenesis promotion, and regenerative wound healing. Leukocyte crosstalk with unique fibroblast subtype(s) is an underexplored area and will be the focus of future studies.

αSMA-expressing post-injury-activated myofibroblasts are well recognized as a major contributor to matrix deposition, contraction, and scar formation following injury^2,5. Conversely, FSP1-expressing fibroblasts, although accepted as post-injury-activated fibroblast, are less appreciated for their role in post-injury healing. Other cell types such as hematopoietic and endothelial cells also express the FSP1 protein following injury⁸, creating ambiguity in assigning a specific role to FSP1-expressing fibroblasts. Due to this, FSP1-expressing cells are mostly considered to be of hematopoietic origin with very little attention to a subset of FSP1⁺ cells that are fibroblasts¹⁰. In the present study, using BMT, we found that the majority of the FSP1⁺ fibroblasts originated at the site of injury and are non-hematopoietic. Freshly sorted non-hematopoietic and non-endothelial FSP1⁺ cells stained positive for fibroblast markers, including MEF-SK4, and negative for pericyte marker AN2/NG2, were ultrastructurally similar to activated fibroblasts, and were able to contract collagen gel similar to uninjured and αSMA⁺ fibroblasts, confirming the fibroblastic phenotype of FSP1⁺ fibroblasts.

In addition, αSMA⁺ and FSP1⁺ fibroblast subtypes proliferated at a similar rate indicating fibroblast heterogeneity is not likely to modulate the post-injury fibroblast proliferation, consistent with work done by others⁵⁴. It is possible that shared molecular mechanism(s) stimulate the activation and proliferation of both fibroblast subtypes. Our observation that both αSMA⁺ and FSP1⁺ fibroblasts respond to pro-fibrotic proteins, TGFβ and WNT3A, supports this argument.

We found that both activated fibroblast subtypes express COL1A1 and periostin. Although, COL1A1 is known to be highly expressed by myofibroblasts, its presence is not unique to fibroblasts and myofibroblasts⁵⁵. Conversely, lineage tracing studies in the damaged heart have shown that periostin is expressed by a majority of myofibroblasts following MI but is not expressed to a similar extent by FSP1⁺ fibroblasts^8,10. The reason for this discrepancy could be due to the presence of other FSP1-expressing cell types, which may have masked the presence of FSP1-expressing fibroblasts. We excluded other cell subsets in our isolation to obtain an active periostin and MEF-SK4 expressing FSP1⁺ fibroblast population. The presence and functional role of periostin in wound remodeling has been documented⁵⁶ and its presence in the two activated fibroblast subtypes suggests that both FSP1⁺ and αSMA⁺ fibroblasts actively participate in the wound repair and remodeling process. Whereas MEF-SK4 has been shown to be a reliable fibroblast marker irrespective of their activation state²³.

We took two approaches to identify the transcriptional profiles of these two fibroblast subsets. The fibrosis gene expression array provided a comprehensive and focused view on the gene signature variation involved in the fibrotic process whereas RNA sequencing presented a detailed transcriptional snapshot while confirming the fibrosis array data. Elevated expression of genes involved in matrix synthesis and the TGFβ signaling pathway have been known to be a hallmark of the myofibroblast phenotype^24,25,40. The cardiac FSP1⁺ fibroblast transcript signature has not been characterized in detail. Expression of matrix synthesis genes to a lesser extent in FSP1⁺ fibroblasts than in αSMA⁺ fibroblasts suggests that the FSP1⁺ fibroblast lacks a strong fibrotic phenotype compared with αSMA⁺ fibroblasts. This premise was supported by the identification that several genes that are involved in promoting fibrosis, such as Il1b, Ccr2, Ccl12 (a ligand for Ccr2), Cxcr4, and Tnf, were downregulated in FSP1⁺ fibroblasts in comparison with αSMA⁺ fibroblasts favoring a predominant role of FSP1⁺ fibroblasts in reparative vs. fibrotic wound healing^57,58,59,60.

Fibroblasts contribute to both physiological and pathological angiogenesis^61,62. While fibroblast activation has been largely focused on the periostin and αSMA-expressing myofibroblast phenotype^2,5, FSP1-expressing activated fibroblasts were shown to support a pro-angiogenic microenvironment in breast cancer metastasis⁶³. According to this report, secreted growth factors expressed by FSP1⁺ cells and ECM proteins played key roles in metastatic colonization. This study supports our findings of the pro-angiogenic role of FSP1⁺ fibroblasts during fibrotic wound healing. Interestingly, the role of FSP1 protein in promoting angiogenesis has been documented by others in tumor angiogenesis^31,32 but not in wound repair. However, our findings demonstrated that the pro-angiogenic effects of FSP1⁺ fibroblasts observed in vivo and in vitro using their secretome (conditioned media) was more robust than that induced just by recombinant FSP1 protein. These observations suggest that the pro-angiogenic effect of FSP1-expressing fibroblast secretome was due to the combined effects of FSP1 protein itself as well as other factors. Angiogenesis requires the concerted action of multiple cytokines and growth factors⁶⁴ that were evident in FSP1⁺ fibroblasts based upon the angiogenesis proteome array analysis. In addition to Vegfa and Vegfb, we identified other pro-angiogenic factors, including Grem1, Angpt1, and Fgf1, that were robustly expressed in FSP1⁺ fibroblasts. This indicates a strong pro-angiogenic signature presented by FSP1-expressing fibroblasts. Although VEGFA, VEGFB, ANGIOPOETIN 1, and FGF1 proteins are hallmarks of angiogenesis^65,66, the significance of GREM1 in promoting angiogenesis has received attention by only a few elegant studies^67,68. The orchestrated effort of multiple pro-angiogenic factors, including GREM1, in imparting a functional role to FSP1⁺ fibroblasts needs to be explored in future studies. Altogether, both molecular and biochemical data in vitro as well as a wound healing model in vivo suggest a pro-angiogenic phenotype in FSP1⁺ fibroblasts.

We identified two distinct activated fibroblast subtypes in several forms of tissue repair. The FSP1⁺ fibroblast subset appears to play a significant role in promoting angiogenesis and possibly regenerative wound healing. The FSP1⁺ population is distinct from the well-established, injury-activated αSMA⁺ myofibroblasts. The heterogeneity of activated fibroblasts likely reflects the complex nature of organ repair and fibrosis, and it may also explain the failure to develop a robust anti-fibrotic therapy that overlooks such functional heterogeneity. Our studies serve to clarify the functional and molecular uniqueness of two distinct but prevalent post-injury fibroblast subtypes with the hope that greater understanding will lead to improved therapeutic targeting to mitigate fibrosis without altering functions necessary for wound healing.

Methods

Animals

Wild-type C57Bl/6 (WT) mice were purchased from Jackson Laboratory (Bar Harbor, ME, http://www.jax.org). GFP-FSP1 and GFP-SMA mice were generous gifts from Drs. William E. Lawson (generated by Dr. Eric Neilson²⁰) and Ivo Kalajzic²¹, respectively. This study was carried out in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The Vanderbilt University Institutional Animal Care and Use Committee approved the protocol (Protocol number: M1600076-00). This study complies with all relevant ethical regulations. All experiments were performed using appropriate analgesics and anesthetics, and every effort was made to minimize pain/distress.

Bone marrow transplantation (BMT)

Unfractionated BM was obtained from C57Bl/6 mice⁶⁹. FSP1-GFP mice were preconditioned with 10 Gy of γ-radiation from a 137Cs source before intraperitoneal injection with 5 × 10⁶ nucleated donor cells obtained from C57/BL6 mice. Recipient mice were given 2 months for recovery and engraftment post transplant before MI was performed.

Myocardial infarction

MI surgeries were performed at the Cardiovascular Physiology Core at Vanderbilt University Medical Center. For the MI model, mice were anesthetized with sodium pentathol (50 mg/kg) and endotracheal intubation was performed under direct laryngoscopy. Mice were ventilated with a small animal respirator (tidal volume = 1.0 ml, rate = 110 breaths/min). With the use of a surgical microscope, a left thoracotomy was performed. The fourth intercostal space was entered using scissors and blunt dissection. A 7-0 silk suture was placed through the myocardium into anterolateral LV wall (around the left anterior descending artery) and the artery ligated. Each heart was monitored with continuous EKG throughout the procedure to ensure successful infarction. The chest was closed in layers with 6-0 silk and the animal was gradually weaned from the respirator to avoid complicating pneumothorax. Intraperitoneal administration of buprenorphine (0.1 mg/kg) immediately following surgery and every 8–12 h for 72 h post surgery was used as analgesic. Animals were monitored closely for signs of distress and weight loss throughout the study period. Following study completion, or upon distress, animals were euthanized by overdose of isoflurane followed by cervical dislocation.

Human heart tissues were collected from cadavers without MI as well as from cadavers who passed away within 2 weeks post MI. Paraffin blocks of postmortem human heart tissue were obtained from the Vanderbilt Medical Center Tissue Repository through VUMC Cardiovascular Translational and Clinical Research (CLTCR) via IRB approval (Vanderbilt IRB No: 130881). Informed consent was obtained with consent for autopsy to use the postmortem tissues for research in a de-identified manner. Experiments with these tissues were performed in adherence to the relevant ethical guidelines. Patient de-identified paraffin embedded slides of human hearts were generated at Translational Pathology Shared Resource (TPSR) Vanderbilt University Medical Center.

Cell culture

Human umbilical vein endothelial cells (HUVECs) were purchased from Lonza (C2519A; pooled donor) and were maintained in EBM-2^TM (Lonza; CC-3156) media supplemented with EGM-2^TM Single Quots (Lonza; CC-4176), fungizone and antibiotics. Human retinal pericytes (Cell Systems ACBRI 183), generous gift from Dr. John Penn’s lab, were maintained in DMEM supplemented with 10% FBS and EGM-2^TM Single Quots. Primary murine pulmonary microvascular endothelial cells were isolated and generously shared by Dr. Jin Chen’s laboratory⁷⁰. Primary uninjured, FSP1⁺ and αSMA⁺ fibroblasts were isolated and sorted from murine hearts and cultured in DMEM-F12 with 10% FBS at 37 °C/5% CO₂. In some experiments, cells (P3–P5) were treated with TGFβ (10 ng/ml; R&D Systems: 240-B-010) or WNT3A (50 ng/ml; R&D Systems: 1324-WN) or PDGFβ (1:1000; Gibco: PHG004), or FGF-2 (25 ng/ml; Prospec: cyt-386) for 24 h.

Primary fibroblast isolation

Primary mouse cardiac fibroblasts were isolated according to previous protocol¹⁰. Uninjured C57Bl/6 mice were used to isolate uninjured fibroblasts whereas FSP1-GFP and αSMA-GFP mice were used to isolate and sort GFP-expressing fibroblasts 10 days following MI. In short, mice at least 12-weeks-old were euthanized by overdose of isoflurane followed by cervical dislocation. Heart tissue was dissected to isolate ventricular tissue, which was then placed into Kreba-Henseleit (KHB; Sigma; K3753a) buffer with 2.9 mM CaCl₂ and 24 mM NaHCO₃ and quickly minced. The minced tissue was then transferred to a digestion cocktail of 0.25 mg/mL Liberase Blendzyme 3 (Roche Applied Science), 20 U/mL DNase I (Sigma Aldrich), 10 mmol/L HEPES (Invitrogen), and 0.1% sodium azide in HBSS and stirred at 37 °C for 20 min. Cells collected after digestion were passed through 40 μm filter and centrifuged at 400 × g for 15 min. To remove red blood cells, cell pellet was resuspended in 1 ml of Red Blood Cell lysis buffer and incubated for 1 min. Following incubation, cells were washed with the KHB buffer and centrifuged at 400 × g for 15 min. Cells were resuspended in DMEM-F12 with 10% FBS. For uninjured fibroblast isolation, cells were plated into 6-well dish for separation of fibroblasts by selective adhesion for 4 h. Unattached and dead cells were washed with PBS and fresh media was added to the attached fibroblast for culture. For FSP1 and αSMA-expressing fibroblasts isolation, GFP-expressing cells were sorted by fluorescence assisted cell sorting (FACS) as described in the “Flow cytometry” section.

Flow cytometry

Isolated αSMA⁺ or FSP1⁺ fibroblasts were flow sorted for green fluorescent protein (GFP) 10 days following MI. Dead cells were excluded by either using 7AAD (Molecular Probes: A13010) or Ghost dye^TM violet 510 (13-0870; Tonbo Biosciences). Unstained uninjured fibroblasts were used to set the background signal in the GFP channel post compensation. A gate was drawn to capture all cells producing a larger voltage pulse area than the established background in the GFP channel. GFP⁺ FSP1 cells were gated with APC-CD45 (1:200; BD Bioscience: 559864) and PE-CD31 (1:200; BD Bioscience: 553373) antibodies to exclude FSP1-expressing endothelial and hematopoietic cells. For αSMA-GFP mice, live GFP-positive cells were selected by gating for 7-AAD or Ghost dye^TM violet 510-negative, GFP-positive cells.

For analyses, cells were incubated with Fc blocker (purified anti-mouse CD16/CD32 (2.4G2; 70-0161; Tonbo Biosciences) prior to staining with the following antibodies: anti-feeder cells-APC (MEF-SK4) (1:10; Miltenyi Biotec: 130-102-900), anti-AN2/NG2 (1:11; Miltenyi Biotec: 130-097-455), APC-CD45, or PE-CD31 for 30 min 7AAD (1:1000; Molecular Probes: A13010) or Ghost dye^TM violet 510 (1:1000; 13-0870; Tonbo Biosciences) were used to exclude dead cells. For unconjugated antibodies, donkey anti-rat alexa fluor 647 (1:100; Abcam: ab175670) secondary antibody was used. Flow cytometry analyses were performed in the VMC Flow Cytometry Shared Resource.

Concentration of condition media

In total, 1 × 10⁶ FSP1⁺, αSMA⁺, or uninjured primary fibroblast cells (P3–P5) were plated in 10 cm² dishes in DMEM-F12 containing 10% FBS. After cells attached, media was exchanged for DMEM F12 with 0.5% FBS or alternatively with EBM-2 containing 0.2% FBS and incubated at 37 °C for 72 h. Conditioned media (CM) was collected and then concentrated by centrifugation at 3500 × g with the help of Amicon Ultra centrifugal filter units (Millipore: UFC900324) for 30 min. Protein concentration was assessed by bicinchoninic acid assay (BCA assay). CM generated in EBM-2 was used to treat HUVECs for proliferation and endothelial cell assembly assays.

Enzyme linked immunosorbent assay (ELISA)

The Quantikine mouse VEGF ELISA kit (R&D Systems; #MMV00) and Gremlin-1 ELISA kit (Raybiotech # ELM-GREM1) were utilized to quantify VEGF or Gremlin-1 in conditioned media (100 µg/cell type) or cell extracts (50 µg/cell type) of fibroblast subtypes (P3–P5). All assays were performed in triplicate according to each manufacturer’s instructions.

Angiogenesis protein array

The Proteome Profiler Mouse Angiogenesis Array Kit (# ARY015; R & D) was used to assess the relative levels of 53 mouse angiogenesis-related proteins in 300 µg of FSP1⁺ and αSMA⁺ cell lysates according to manufacturer’s instructions. Angiogenesis Array is a membrane-based sandwich immunoassay. The cells were cultured for 72 h in 0.5% FBS prior to protein collection. Briefly, a cocktail of biotinylated detection antibodies was mixed with cell lysates. The array membrane was then treated with the cell lysate and antibody mixture overnight at 4 °C, washed, and then incubated with streptavidin-HRP. The array membrane is spotted with capture antibodies to specific target proteins. The captured proteins were visualized using chemiluminescence.

In vitro vascular assembly assay

HUVECS (P5) were serum starved with EBM-2 containing 0.2% FBS overnight, then treated with CellTracker™ Orange CMRA Dye (C34551; Life Technologies) for 1 h at 37 °C. Twenty-four well plates were coated with 150 μl of matrigel (Corning: CB-40230) for 1 h at 37 °C. Following incubation, 3 × 10⁴ HUVECS were seeded into each well with conditioned media collected from either FSP⁺, αSMA⁺, or uninjured fibroblasts. After 16 h, images (×4 and ×10) were taken using an Olympus CK40 inverted microscope through an Optronics DEI-750C charge-coupled device video camera using Cellsens Dimension software. Vascular assembly was assessed by counting the number of intersecting branches⁷⁰.

Cell proliferation assays

Cell proliferation was assessed by 5-bromo-2′-deoxyuridine (BrdU) cell proliferation assay (Calbiochem, Gibbstown, NJ). Following serum starvation, 2000 HUVECs (p5) or 1000 fibroblasts (P3–P5) were seeded per well in a 96-well plate. Following overnight attachment of cells to plate, media was replaced with fibroblast conditioned media (FSP1⁺, αSMA⁺, and uninjured). In some experiments, HUVECs were treated with 10 nM recombinant mouse S100A4 protein (R&D Systems: 4138-S4-050). BrdU incorporation was assessed by measured absorbance at dual wavelength of 450/595 nm following manufacture’s protocol.

Repair/granulation tissue stimulation

PVA sponges (Medtronics Merocel (4 mg, 2 mm height, 4 mm diameter)) were soak loaded with freshly sorted 7.5 × 10⁵ primary FSP1⁺ or αSMA⁺ fibroblasts in 20 µl of sterile PBS and were implanted in ventral subcutaneous pockets of adult C57Bl/6 mice. Mice were taken down at day 14 after implantation to remove the sponges. The sponges were cut in half and fixed in 10% neutral buffered formalin for 24 h, embedded cut side down in paraffin and sectioned for immunostaining.

Histochemistry and morphometry

Sponges embedded in paraffin were sectioned into 5-micron-thick transverse sections for histology. Vanderbilt Translational Pathology Shared Resource performed the immunohistochemistry for CD31 to analyze vascularity with anti-CD31/platelet endothelial cell adhesion molecule-1 (PECAM-1; clone 557355, PharMingen)⁶⁹. Images of CD31 stained sections were obtained with a CoolSNAP Hq CCD camera (Photometrics). Five images from each section were acquired at defined magnification (×40) for vascular density. Each field was quantified using Image J (NIH) by outlining tissue and calculating percentage CD31⁺ area per field.

Immunofluorescence and immunohistochemistry

Immunofluorescence staining was performed on cells as well as on paraffin embedded tissues. Primary fibroblasts (P0–P1) were seeded and cultured on coverslips until 80% confluent prior to immunostaining. In some cases, uninjured, αSMA⁺, and FSP1⁺ fibroblasts were treated with 10 ng/ml TGFβ for 72 h prior to fixation and immunostaining. Sorted primary GFP⁺/CD45⁺ and GFP⁺/CD31⁺ cells were concentrated on a coverslip by cytospin for immunostaining. Cells were fixed with cold acetone for 15 min and washed three times with PBS. For tissue staining, slides were deparaffinized and hydrated through a series of xylene and ethanol baths. Heat-mediated antigen retrieval was performed by boiling in citrate buffer (pH 6). Slides/coverslips were blocked in 10% goat serum and incubated with primary antibodies overnight. Secondary antibody incubation was performed for 2 h after three washes with PBS. The slides were counterstained and mounted using DAPI in slow-fade mounting media (Invitrogen: P36931). The following primary antibodies were used: Fibroblast-specific protein 1 (FSP1) (1:100; Millipore: 07-2274), α-smooth muscle actin (αSMA) (1:1000; Sigma: A2547), COL1α1 (1:1000; MD Bioproducts: 203002), Periostin (1:100; Santa Cruz: SC67233), Vimentin (1:200; Sigma: V2258), CD31 (1:250; BD Biosciences: 553370), CD45 (1:250; BD Biosciences: 553076), AN2/NG2 (1:100; Invitrogen: MA5-24247), VWF Polyclonal Antibody (Thermo-Fisher; Cat No: PA5-16634), and VEGFR2 (Flk1) SINGLE CHAIN ANTIBODY (Fitzgerald; Cat No: 10R-V106A). The secondary antibodies used were: conjugated goat anti-mouse Alexa Fluor 488 (Molecular Probes: A11029) or goat anti-rabbit-FITC or goat anti-rabbit-Cy3 (Jackson Immunoresearch Laboratories: 711-165-152 or Southern Biotech: 4050-02), goat anti-rat Alexa Fluor 488 or goat anti-rat Alexa Fluor 647 (Molecular Probes: A11006 or; Thermo-Fisher: A21247), or goat anti-chicken-FITC (Jackson Immunoresearch Laboratories: 103-095-155). For confocal analysis, LSM510 (Zeiss) microscope was used to capture 1 µm optical slices (z stack); the images were analyzed using Fiji software. Cells (P0–P1) were used for electron microscopy and pictures were obtained using a Quanta 250 Environmental Electron Microscope.

Collagen contraction assay

For the gel contraction assay 900 µl of collagen solution (1.67 mg/mL Type 1 rat collagen, 20 mM HEPES, 44 mM NaHCO₃, 1× DMEM) was mixed with 100 µl cells (3.3 × 10⁵ cells/mL) (P3–P5) for a final concentration of 1.5 mg/mL collagen. The cell/collagen mix was plated in 48-well plate (300 µl, 10⁵ cells/well) and incubated for 15–20 min at 37 °C until gelled. The gel was separated from the walls of the well with the help of a 30G needle. DMEM (600 µl/well) supplemented with 10% FBS and 1 ng/mL TGFβ (R&D Systems, #76666-MB) was added on top of the gels. Plates were scanned at 0, 24, and 48 h.

Western blot analysis

FSP1⁺ and αSMA⁺ fibroblasts (P3–P5) were serum starved overnight and seeded in DMEM-F12 with 10% FBS at a density of 5 × 10⁵ cells/well in a six-well plate. Cells were washed with PBS and lysed using RIPA buffer supplemented with protease and phosphatase inhibitors (Roche). Cell lysates were rocked for 30 min at 4 °C then centrifuged at 10,000 × g for 15 min to collect the supernatant. Protein concentrations were determined using a bicinchoninic acid (BCA) kit (Thermo Scientific). Fifty micrograms of protein was denatured at 95 °C for 10 min in SDS sample buffer before being resolved on SDS-PAGE electrophoresis and transferred onto a nitrocellulose membrane (PerkinElmer). Blots were blocked in 5% nonfat milk and probed with antibodies against collagen type I (MD Bioproducts, #203002), pSMAD2 (Cell Signaling, #3108L), SMAD2/3 (Cell Signaling, #5678S), LRP6 (Santa Cruz Biotechnology, SC-25317), pLRP6 (Cell Signaling, 2568S), or β-actin (Sigma Aldrich, #A5441). Species-specific secondary antibodies were used and chemiluminescence (NEL104, PerkinElmer, Waltham, MA) was detected by autoradiography.

Semiquantitative real-time PCR

Cells (P3–P5) were snap frozen in Trizol Reagent (Invitrogen, 15596026). Following RNA isolation with the Trizol Reagent, first strand DNA synthesis was performed with 1 µg RNA using iScript cDNA synthesis kit (Bio-Rad 170-8890) and semiquantitative real-time PCR was performed. Each reaction was normalized against 18S. Primers used are listed in Supplementary Table 2 (Table S2).

RNA sequencing

Fibroblasts were isolated and sorted—described in “Primary fibroblast isolation” section—from uninjured, FSP1-GFP and αSMA-GFP mice. Uninjured FBs were isolated from uninfarcted C57Bl/6 mice¹⁰. Enzyme digested cells were seeded on tissue culture plate for 4 h. Unattached cells were washed, and plastic-adherent FBs were collected for RNA extraction. FSP1-GFP and αSMA-GFP fibroblasts were sorted by FACS as described earlier. RNA was prepared from freshly sorted fibroblasts with the help of Ambion RNAqueous™-Micro Total RNA Isolation Kit (Life Technologies).

Purified RNA was sent to Vanderbilt sequencing core (VANTAGE), paired end sequencing was performed at 75X depth. Raw data (FASTQ files) were uploaded to CLC Genomic Workbench 8 (Qiagen) and data quality assessment performed. Sequences were aligned to the Grmc38 platform of the Mus musculus genome using Tuxedo Suite, followed by normalization (RPKM). Data were annotated using Ensemble Release 83 and quantified at the gene level using CuffDiff. Since replicates were not use, proportional-based statistical analysis was performed using Baggerly’s t-test with multiple hypothesis correction. Genes with fold difference of 2 and p value < 0.05 were retained for functional analysis. DAVID bioinformatics Resource 6.7 platform was used for KEGG pathway analysis. The RNA-seq data are available at the NCBI GEO database with the accession number GSE130062.

Fibrosis array

Fibrosis array was performed on freshly isolated and sorted uninjured, FSP1⁺ and αSMA⁺ fibroblasts. RNA was prepared from freshly sorted fibroblasts with the help of Ambion RNAqueous™-Micro Micro Total RNA Isolation Kit (Life Technologies). The first strand cDNA was synthesized with 500 ng of total RNA with the help of RT² First Strand Kit as per manufacturer’s instructions (Qiagen, SABiosciences Corp., Frederick, USA). Samples were diluted with RT² SYBR Green qPCR master mix (SABiosciences Corp.) and pipetted into 96-well Mouse Fibrosis PCR array plates (SABiosciences Corp., Frederick, USA) to perform real time PCR quantification. The assay was performed on a CFX96 Real Time PCR Detection System (Bio-Rad). Each 96-well array plate consists of a panel of 84 genes involved in cardiac fibrosis in addition to house keeping genes and internal controls. Raw data were exported into an excel sheet and analyzed using the integrated web-based automated software available through SABiosciences for PCR Array Data Analysis. Relative gene expression and fold change was calculated by comparative threshold cycle (ΔΔCt) method. A two fold or greater change (p value cutoff < 0.05) in gene expression was considered significant.

Statistical analysis

Statistical significance calculations were performed using unpaired t test, one-way or two-way analysis of variances (ANOVA) with Bonferroni correction for multiple-group comparisons using the Prism 7.02 software (Graph-pad prism). p ≤ 0.05 was considered significant.

Data availibility

The RNA-seq data are available at the NCBI GEO database with the accession number GSE130062. The data from the angiogenesis array are deposited on figshare and can be accessed at https://figshare.com/s/1e573d8d31707884f2b8. All other data supporting the finding of this study are available from the authors on request.

References

Roger, V. L. et al. Heart disease and stroke statistics—2012 update: a report from the American Heart Association. Circulation 125, e2–e220 (2012).
Article Google Scholar
Chen, W. & Frangogiannis, N. G. Fibroblasts in post-infarction inflammation and cardiac repair. Biochim Biophys. Acta 1833, 945–953 (2013).
Article CAS Google Scholar
Duan, J. et al. Wnt1/betacatenin injury response activates the epicardium and cardiac fibroblasts to promote cardiac repair. EMBO J. 31, 429–442 (2012).
Article CAS Google Scholar
Sharpe, N. Cardiac remodeling in coronary artery disease. Am. J. Cardiol. 93, 17B–20B (2004).
Article Google Scholar
Boor, P. & Floege, J. The renal (myo-)fibroblast: a heterogeneous group of cells. Nephrol. Dial. Transpl. 27, 3027–3036 (2012).
Article Google Scholar
Sorrell, J. M. & Caplan, A. I. Fibroblasts-a diverse population at the center of it all. Int Rev. Cell Mol. Biol. 276, 161–214 (2009).
Article Google Scholar
Tallquist, M. D. & Molkentin, J. D. Redefining the identity of cardiac fibroblasts. Nat. Rev. Cardiol. 14, 484–491 (2017).
Article Google Scholar
Kanisicak, O. et al. Genetic lineage tracing defines myofibroblast origin and function in the injured heart. Nat. Commun. 7, 12260 (2016).
Article ADS CAS Google Scholar
Frangogiannis, N. G., Michael, L. H. & Entman, M. L. Myofibroblasts in reperfused myocardial infarcts express the embryonic form of smooth muscle myosin heavy chain (SMemb). Cardiovasc. Res. 48, 89–100 (2000).
Article CAS Google Scholar
Kong, P., Christia, P., Saxena, A., Su, Y. & Frangogiannis, N. G. Lack of specificity of fibroblast-specific protein 1 in cardiac remodeling and fibrosis. Am. J. Physiol. Heart Circ. Physiol. 305, H1363–H1372 (2013).
Article CAS Google Scholar
Zeisberg, E. M., Potenta, S. E., Sugimoto, H., Zeisberg, M. & Kalluri, R. Fibroblasts in kidney fibrosis emerge via endothelial-to-mesenchymal transition. J. Am. Soc. Nephrol. 19, 2282–2287 (2008).
Article Google Scholar
Zeisberg, E. M. et al. Endothelial-to-mesenchymal transition contributes to cardiac fibrosis. Nat. Med 13, 952–961 (2007).
Article CAS Google Scholar
Zhang, J., Chen, L., Xiao, M., Wang, C. & Qin, Z. FSP1 + fibroblasts promote skin carcinogenesis by maintaining MCP-1-mediated macrophage infiltration and chronic inflammation. Am. J. Pathol. 178, 382–390 (2011).
Article CAS Google Scholar
Rock, J. R. et al. Multiple stromal populations contribute to pulmonary fibrosis without evidence for epithelial to mesenchymal transition. Proc. Natl Acad. Sci. USA. 108, E1475–E1483 (2011).
Article CAS Google Scholar
Sugimoto, H., Mundel, T. M., Kieran, M. W. & Kalluri, R. Identification of fibroblast heterogeneity in the tumor microenvironment. Cancer Biol. Ther. 5, 1640–1646 (2006).
Article CAS Google Scholar
Osterreicher, C. H. et al. Fibroblast-specific protein 1 identifies an inflammatory subpopulation of macrophages in the liver. Proc. Natl Acad. Sci. USA. 108, 308–313 (2010).
Article ADS Google Scholar
Alfaro, M. P. et al. A Wnt modulator sFRP2 enhances mesenchymal stem cell engraftment, granulation tissue formation and myocardial repair. Proc. Natl Acad. Sci. USA. 105, 18366–18371 (2008).
Article ADS CAS Google Scholar
Bastakoty, D. et al. Inhibition of Wnt/beta-catenin pathway promotes regenerative repair of cutaneous and cartilage injury. FASEB J. 29, 4881–4892 (2015).
Article CAS Google Scholar
Gewin, L. et al. TGF-beta receptor deletion in the renal collecting system exacerbates fibrosis. J. Am. Soc. Nephrol. 21, 1334–1343 (2010).
Article CAS Google Scholar
Iwano, M. et al. Evidence that fibroblasts derive from epithelium during tissue fibrosis. J. Clin. Invest. 110, 341–350 (2002).
Article CAS Google Scholar
Kalajzic, Z. et al. Use of an alpha-smooth muscle actin GFP reporter to identify an osteoprogenitor population. Bone 43, 501–510 (2008).
Article CAS Google Scholar
Eyden, B. Fibroblast phenotype plasticity: relevance for understanding heterogeneity in "fibroblastic" tumors. Ultrastruct. Pathol. 28, 307–319 (2004).
Article Google Scholar
Pinto, A. R. et al. Revisiting cardiac cellular composition. Circ. Res 118, 400–409 (2016).
Article CAS Google Scholar
Midgley, A. C. et al. Transforming growth factor-beta1 (TGF-β1)-stimulated fibroblast to myofibroblast differentiation is mediated by hyaluronan (HA)-facilitated epidermal growth factor receptor (EGFR) and CD44 co-localization in lipid rafts. J. Biol. Chem. 288, 14824–14838 (2013).
Article CAS Google Scholar
Thannickal, V. J. et al. Myofibroblast differentiation by transforming growth factor-beta1 is dependent on cell adhesion and integrin signaling via focal adhesion kinase. J. Biol. Chem. 278, 12384–12389 (2003).
Article CAS Google Scholar
Petrov, V. V., Fagard, R. H. & Lijnen, P. J. Stimulation of collagen production by transforming growth factor-beta1 during differentiation of cardiac fibroblasts to myofibroblasts. Hypertension 39, 258–263 (2002).
Article CAS Google Scholar
Bonner, J. C. Regulation of PDGF and its receptors in fibrotic diseases. Cytokine Growth Factor Rev. 15, 255–273 (2004).
Article CAS Google Scholar
Detillieux, K. A., Sheikh, F., Kardami, E. & Cattini, P. A. Biological activities of fibroblast growth factor-2 in the adult myocardium. Cardiovasc. Res. 57, 8–19 (2003).
Article CAS Google Scholar
Gray, M. O., Long, C. S., Kalinyak, J. E., Li, H. T. & Karliner, J. S. Angiotensin II stimulates cardiac myocyte hypertrophy via paracrine release of TGF-beta 1 and endothelin-1 from fibroblasts. Cardiovasc. Res. 40, 352–363 (1998).
Article CAS Google Scholar
Stein, U. et al. The metastasis-associated gene S100A4 is a novel target of beta-catenin/T-cell factor signaling in colon cancer. Gastroenterology 131, 1486–1500 (2006).
Article CAS Google Scholar
Ambartsumian, N. et al. The metastasis-associated Mts1(S100A4) protein could act as an angiogenic factor. Oncogene 20, 4685–4695 (2001).
Article CAS Google Scholar
Ochiya, T., Takenaga, K. & Endo, H. Silencing of S100A4, a metastasis-associated protein, in endothelial cells inhibits tumor angiogenesis and growth. Angiogenesis 17, 17–26 (2014).
Article CAS Google Scholar
Davidson, J. M. et al. Accelerated wound repair, cell proliferation, and collagen accumulation are produced by cartilage derived growth factor. J. Cell Biol. 100, 1219–1227 (1985).
Article CAS Google Scholar
Driskell, R. R. et al. Distinct fibroblast lineages determine dermal architecture in skin development and repair. Nature 504, 277–281 (2013).
Article ADS CAS Google Scholar
Phipps, R. P. et al. Characterization of two major populations of lung fibroblasts: distinguishing morphology and discordant display of Thy 1 and class II MHC. Am. J. Respir. Cell Mol. Biol. 1, 65–74 (1989).
Article CAS Google Scholar
Rinkevich, Y. et al. Skin fibrosis. Identification and isolation of a dermal lineage with intrinsic fibrogenic potential. Science 348, aaa2151 (2015).
Article Google Scholar
Park, J. et al. Single-cell transcriptomics of the mouse kidney reveals potential cellular targets of kidney disease. Science 360, 758–763 (2018).
Article CAS Google Scholar
Philippeos, C. et al. Spatial and single-cell transcriptional profiling identifies functionally distinct human dermal fibroblast subpopulations. J. Invest. Dermatol. 138, 811–825 (2018).
Article CAS Google Scholar
Skelly, D. A. et al. Single-cell transcriptional profiling reveals cellular diversity and intercommunication in the mouse. Heart Cell Rep. 22, 600–610 (2018).
Article CAS Google Scholar
Powell, D. W. et al. Myofibroblasts. I. Paracrine cells important in health and disease. Am. J. Physiol. 277, C1–C9 (1999).
Article CAS Google Scholar
White, E. S. Lung extracellular matrix and fibroblast function. Ann. Am. Thorac. Soc. 12(Suppl 1), S30–S33 (2015).
Article Google Scholar
Barker, T. H. et al. Thy-1 regulates fibroblast focal adhesions, cytoskeletal organization and migration through modulation of p190 RhoGAP and Rho GTPase activity. Exp. Cell Res. 295, 488–496 (2004).
Article CAS Google Scholar
Koumas, L., King, A. E., Critchley, H. O., Kelly, R. W. & Phipps, R. P. Fibroblast heterogeneity: existence of functionally distinct Thy 1(+) and Thy 1(−) human female reproductive tract fibroblasts. Am. J. Pathol. 159, 925–935 (2001).
Article CAS Google Scholar
McIntosh, J. C., Hagood, J. S., Richardson, T. L. & Simecka, J. W. Thy1 (+) and (−) lung fibrosis subpopulations in LEW and F344 rats. Eur. Respir. J. 7, 2131–2138 (1994).
Article CAS Google Scholar
Mizoguchi, F. et al. Functionally distinct disease-associated fibroblast subsets in rheumatoid arthritis. Nat. Commun. 9, 789 (2018).
Article ADS Google Scholar
Czubryt, M. P. Common threads in cardiac fibrosis, infarct scar formation, and wound healing. Fibrogenes. Tissue Repair 5, 19 (2012).
Article Google Scholar
Meran, S. & Steadman, R. Fibroblasts and myofibroblasts in renal fibrosis. Int. J. Exp. Pathol. 92, 158–167 (2011).
Article CAS Google Scholar
Jung, M. et al. IL-10 improves cardiac remodeling after myocardial infarction by stimulating M2 macrophage polarization and fibroblast activation. Basic Res. Cardiol. 112, 33 (2017).
Article Google Scholar
Lin, Z. Q., Kondo, T., Ishida, Y., Takayasu, T. & Mukaida, N. Essential involvement of IL-6 in the skin wound-healing process as evidenced by delayed wound healing in IL-6-deficient mice. J. Leukoc. Biol. 73, 713–721 (2003).
Article CAS Google Scholar
Toriseva, M. et al. MMP-13 regulates growth of wound granulation tissue and modulates gene expression signatures involved in inflammation, proteolysis, and cell viability. PLoS ONE 7, e42596 (2012).
Article ADS CAS Google Scholar
Zheng, L. et al. Matrix metalloproteinase-3 accelerates wound healing following dental pulp injury. Am. J. Pathol. 175, 1905–1914 (2009).
Article CAS Google Scholar
Hunt, T. K., Knighton, D. R., Thakral, K. K., Goodson, W. H. 3rd & Andrews, W. S. Studies on inflammation and wound healing: angiogenesis and collagen synthesis stimulated in vivo by resident and activated wound macrophages. Surgery 96, 48–54 (1984).
CAS PubMed Google Scholar
Van Linthout, S., Miteva, K. & Tschope, C. Crosstalk between fibroblasts and inflammatory cells. Cardiovasc. Res. 102, 258–269 (2014).
Article Google Scholar
Ali, S. R. et al. Developmental heterogeneity of cardiac fibroblasts does not predict pathological proliferation and activation. Circ. Res. 115, 625–635 (2014).
Article CAS Google Scholar
Bax, N. A. et al. Matrix production and remodeling capacity of cardiomyocyte progenitor cells during in vitro differentiation. J. Mol. Cell Cardiol. 53, 497–508 (2012).
Article CAS Google Scholar
Shimazaki, M. et al. Periostin is essential for cardiac healing after acute myocardial infarction. J. Exp. Med. 205, 295–303 (2008).
Article CAS Google Scholar
Chu, P. Y. et al. CXCR4 antagonism attenuates the development of diabetic cardiac fibrosis. PLoS ONE 10, e0133616 (2015).
Article Google Scholar
Kolb, M., Margetts, P. J., Anthony, D. C., Pitossi, F. & Gauldie, J. Transient expression of IL-1beta induces acute lung injury and chronic repair leading to pulmonary fibrosis. J. Clin. Invest 107, 1529–1536 (2001).
Article CAS Google Scholar
Moore, B. B. et al. The role of CCL12 in the recruitment of fibrocytes and lung fibrosis. Am. J. Respir. Cell Mol. Biol. 35, 175–181 (2006).
Article CAS Google Scholar
Sun, M. et al. Tumor necrosis factor-alpha mediates cardiac remodeling and ventricular dysfunction after pressure overload state. Circulation 115, 1398–1407 (2007).
Article CAS Google Scholar
Benyahia, Z. et al. Stromal fibroblasts present in breast carcinomas promote tumor growth and angiogenesis through adrenomedullin secretion. Oncotarget 8, 15744–15762 (2017).
Article Google Scholar
Newman, A. C., Nakatsu, M. N., Chou, W., Gershon, P. D. & Hughes, C. C. The requirement for fibroblasts in angiogenesis: fibroblast-derived matrix proteins are essential for endothelial cell lumen formation. Mol. Biol. Cell 22, 3791–3800 (2011).
Article CAS Google Scholar
O'Connell, J. T. et al. VEGF-A and Tenascin-C produced by S100A4 + stromal cells are important for metastatic colonization. Proc. Natl Acad. Sci. USA. 108, 16002–16007 (2011).
Article ADS CAS Google Scholar
Bodnar, R. J. Chemokine regulation of angiogenesis during wound healing. Adv. Wound Care 4, 641–650 (2015).
Article Google Scholar
Shibuya, M. Vascular endothelial growth factor (VEGF) and its receptor (VEGFR) signaling in angiogenesis: a crucial target for anti- and pro-angiogenic therapies. Genes & Cancer 2, 1097–1105 (2011).
Article Google Scholar
Tonnesen, M. G., Feng, X. & Clark, R. A. Angiogenesis in wound healing. J. Invest. Dermatol. Symp . Proc. 5, 40–46 (2000).
Article CAS Google Scholar
Chen, M. H. et al. Expression of gremlin 1 correlates with increased angiogenesis and progression-free survival in patients with pancreatic neuroendocrine tumors. J. Gastroenterol. 48, 101–108 (2013).
Article ADS CAS Google Scholar
Mitola, S. et al. Gremlin is a novel agonist of the major proangiogenic receptor VEGFR2. Blood 116, 3677–3680 (2010).
Article CAS Google Scholar
Young, P. P., Hofling, A. A. & Sands, M. S. VEGF increases engraftment of bone marrow-derived endothelial progenitor cells (EPCs) into vasculature of newborn murine recipients. Proc. Natl Acad. Sci. USA. 99, 11951–11956 (2002).
Article ADS CAS Google Scholar
Wang, S. et al. Regulation of endothelial cell proliferation and vascular assembly through distinct mTORC2 signaling pathways. Mol. Cell. Biol. 35, 1299–1313 (2015).
Article CAS Google Scholar

Download references

Acknowledgements

The authors want to thank Drs. Jeffrey M. Davidson and Hind Lal for careful reading of the manuscript and their critical feedback. We also want to thank David K. Flaherty from Vanderbilt Flow Cytometry Shared Resource and Dr. Shan Wang from Division of Rheumatology and Immunology at the Vanderbilt University Medical Center for their input in flow cytometry data analysis and presentation. We thank Drs. William E. Lawson and Eric Neilson for providing FSP1-GFP mice and Ivo Kalajzic for the gift of αSMA-GFP mice. Research reported in this publication was supported by the National Institute of General Medical Sciences of the National Institutes of Health (NIH) under Award Number R01GM118300 (S.S.), National Institute of Biomedical Imaging and Bioengineering of the NIH under Award Number R21EB019509 (P.P.Y.), National Blood Foundation Grant (S.S.), and Scientist Development Grant of the American Heart Association under Award Number 17SDG33630187 (S.S.). Confocal imaging and electron microscopy analyses were performed in part using the VU Cell Imaging Shared Resource (supported by NIH grants CA68485, DK20593, DK58404, DK59637, and EY08126). Flow cytometry analyses were performed at the VMC Flow Cytometry Shared Resource which is supported by the Vanderbilt Ingram Cancer Center (P30 CA68485) and the Vanderbilt Digestive Disease Research Center (DK058404). The Vanderbilt VANTAGE Core provided technical assistance for RNA sequencing work. VANTAGE is supported in part by CTSA Grant (5UL1 RR024975-03), the Vanderbilt Ingram Cancer Center (P30 CA68485), the Vanderbilt Vision Center (P30 EY08126), and NIH/NCRR (G20 RR030956).

Author information

Authors and Affiliations

Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN, 37232, USA
Sarika Saraswati, Stephanie M. W. Marrow, Lester A. Watch & Pampee P. Young
American Red Cross, National Headquarters, Washington, DC, 20006, USA
Pampee P. Young

Authors

Sarika Saraswati
View author publications
You can also search for this author in PubMed Google Scholar
Stephanie M. W. Marrow
View author publications
You can also search for this author in PubMed Google Scholar
Lester A. Watch
View author publications
You can also search for this author in PubMed Google Scholar
Pampee P. Young
View author publications
You can also search for this author in PubMed Google Scholar

Contributions

P.P.Y. and S.S. designed the experiments. S.S., S.M., and L.W. performed the experiments. P.P.Y., S.S., and S.M. analyzed the data and interpreted the results and wrote the paper.

Corresponding authors

Correspondence to Sarika Saraswati or Pampee P. Young.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Peer review information: Nature Communications thanks the anonymous reviewers for their contribution to the peer review of this work. Peer reviewer reports are available.

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Supplementary Information

Peer Review File

Reporting summary

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and permissions

About this article

Cite this article

Saraswati, S., Marrow, S.M.W., Watch, L.A. et al. Identification of a pro-angiogenic functional role for FSP1-positive fibroblast subtype in wound healing. Nat Commun 10, 3027 (2019). https://doi.org/10.1038/s41467-019-10965-9

Download citation

Received: 29 December 2017
Accepted: 04 June 2019
Published: 09 July 2019
DOI: https://doi.org/10.1038/s41467-019-10965-9

This article is cited by

Cardiac fibroblast GSK-3α aggravates ischemic cardiac injury by promoting fibrosis, inflammation, and impairing angiogenesis
- Prachi Umbarkar
- Suma Ejantkar
- Hind Lal
Basic Research in Cardiology (2023)
Role of fibroblast plasticity and heterogeneity in modulating angiogenesis and healing in the diabetic foot ulcer
- Vikrant Rai
- Rebecca Moellmer
- Devendra K. Agrawal
Molecular Biology Reports (2023)
eEF2 improves dense connective tissue repair and healing outcome by regulating cellular death, autophagy, apoptosis, proliferation and migration
- Junyu Chen
- Jin Wang
- Paul W. Ackermann
Cellular and Molecular Life Sciences (2023)
Effects of histone acetyltransferase (HAT) and histone deacetylase (HDAC) inhibitors on proliferative, differentiative, and regenerative functions of Toll-like receptor 2 (TLR-2)-stimulated human dental pulp cells (hDPCs)
- Sarah Hossam Fahmy
- Holger Jungbluth
- Jochen Winter
Clinical Oral Investigations (2023)
Suppression of PFKFB3-driven glycolysis restrains endothelial-to-mesenchymal transition and fibrotic response
- Hao Zeng
- Ting Pan
- Ping Li
Signal Transduction and Targeted Therapy (2022)

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.