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10.3390/jcdd5020019

http://scihub22266oqcxt.onion/10.3390/jcdd5020019
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C6023394!6023394!29652803
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suck abstract from ncbi


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pmid29652803      J+Cardiovasc+Dev+Dis 2018 ; 5 (2): ä
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  • Hypoxia Supports Epicardial Cell Differentiation in Vascular Smooth Muscle Cells through the Activation of the TGF? Pathway #MMPMID29652803
  • Tao J; Barnett JV; Watanabe M; Ramírez-Bergeron D
  • J Cardiovasc Dev Dis 2018[Jun]; 5 (2): ä PMID29652803show ga
  • Epicardium-derived cells (EPDCs) are an important pool of multipotent cardiovascular progenitor cells. Through epithelial-to-mesenchymal-transition (EMT), EPDCs invade the subepicardium and myocardium and further differentiate into several cell types required for coronary vessel formation. We previously showed that epicardial hypoxia inducible factor (HIF) signaling mediates the invasion of vascular precursor cells critical for patterning the coronary vasculature. Here, we examine the regulatory role of hypoxia (1% oxygen) on EPDC differentiation into vascular smooth muscle cells (VSMCs). Results: Hypoxia stimulates EMT and enhances expression of several VSMC markers in mouse epicardial cell cultures. This stimulation is specifically blocked by inhibiting transforming growth factor-beta (TGF?) receptor I. Further analyses indicated that hypoxia increases the expression level of TGF?-1 ligand and phosphorylation of TGF? receptor II, suggesting an indispensable role of the TGF? pathway in hypoxia-stimulated VSMC differentiation. We further demonstrate that the non-canonical RhoA/Rho kinase (ROCK) pathway acts as the main downstream effector of TGF? to modulate hypoxia?s effect on VSMC differentiation. Conclusion: Our results reveal a novel role of epicardial HIF in mediating coronary vasculogenesis by promoting their differentiation into VSMCs through noncanonical TGF? signaling. These data elucidate that patterning of the coronary vasculature is influenced by epicardial hypoxic signals.
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