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FGF signalling specifies haematopoietic stem cells through its regulation of somitic Notch signalling
In zebrafish embryos, Wnt and Notch signalling have been implicated in the emergence of haematopoietic stem cells during somitogenesis. Here the authors show that FGF signalling via FGFR4 acts downstream of Wnt signalling to regulate the levels of the Notch ligand DeltaC and therefore Notch pathway activity.
- Yoonsung Lee
- , Jennifer E. Manegold
- & David Traver
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| Open AccessDynamic haematopoietic cell contribution to the developing and adult epicardium
The murine epicardium forms an envelope around the heart and contains cells that can participate in cardiac repair. Here the authors discover a population of epicardial cells derived from blood cells, which proliferate and change their surrounding extracellular matrix in response to cardiac injury.
- Gemma M. Balmer
- , Sveva Bollini
- & Paul R. Riley
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Inhibition of endothelial ERK signalling by Smad1/5 is essential for haematopoietic stem cell emergence
Vertebrate haematopoietic stem cells are produced from the haemogenic endothelium by an endothelial-to-haematopoietic transition. Here, the authors show that, in zebrafish and mice, this transition depends on interplay of Smad transcription factors and the ERK signalling pathway.
- Chunxia Zhang
- , Junhua Lv
- & Feng Liu
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Early dynamic fate changes in haemogenic endothelium characterized at the single-cell level
Haematopoietic stem cells emerge from the haemogenic endothelium via an endothelial-to-haematopoietic transition. Here, the authors show using single cell functional and transcriptional analyses that haemogenic endothelial cells begin to lose their endothelial potential while still located within the haemogenic endothelium.
- Gemma Swiers
- , Claudia Baumann
- & Marella F. T. R. de Bruijn
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| Open AccessmiRNomes of haematopoietic stem cells and dendritic cells identify miR-30b as a regulator of Notch1
Several microRNAs have been implicated in the differentiation of immune cells. Here the authors analyse the global microRNA expression profiles of mouse haematopoietic stem cells and different stages of dendritic cell development and identify Notch1 as a target of miR-30b in regulatory dendritic cells.
- Xiaoping Su
- , Cheng Qian
- & Xuetao Cao
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Fate tracing reveals hepatic stellate cells as dominant contributors to liver fibrosis independent of its aetiology
Myofibroblasts drive fibrogenesis in the liver but their cellular origins remain unclear. Here Mederacke et al. use the Lratgene to label hepatic stellate cells (HSCs) in transgenic mice and reveal HSCs as the major source of myofibroblasts in models of toxic, biliary and fatty liver fibrosis.
- Ingmar Mederacke
- , Christine C. Hsu
- & Robert F. Schwabe
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| Open AccessPAD4 regulates proliferation of multipotent haematopoietic cells by controlling c-myc expression
Histone citrullination by peptidylarginine deiminase 4 (PAD4) regulates transcription but its physiological role is unclear. Here Nakashima et al. show that PAD4 controls proliferation of multipotent haematopoietic cells by modulating c-myc expression.
- Katsuhiko Nakashima
- , Satoko Arai
- & Toru Miyazaki
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Klf5 controls bone marrow homing of stem cells and progenitors through Rab5-mediated β1/β2-integrin trafficking
Klf5 is a transcription factor that regulates self-renewal of pluripotent stem cells. Here the authors test the function of Klf5 in somatic stem cells, and discover that it controls stem cell homing and adhesion by regulating endocytosis of beta integrins.
- E. Taniguchi Ishikawa
- , K. H. Chang
- & J. A. Cancelas
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Haematopoietic cells produce BDNF and regulate appetite upon migration to the hypothalamus
Brain-derived neurotrophic factor is produced in the brain and is a known regulator of energy homoeostasis. Here Urabe and colleagues show that brain-derived neurotrophic factor-producing haematopoietic cells control appetite by migrating into the hypothalamus, where they make contact with neurons.
- Hiroshi Urabe
- , Hideto Kojima
- & Hiroshi Kimura