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Platelet-derived growth factor regulates the secretion of extracellular vesicles by adipose mesenchymal stem cells and enhances their angiogenic potential

机译:血小板衍生的生长因子通过脂肪间充质干细胞调节细胞外囊泡的分泌并增强其血管生成潜力

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Background Several studies demonstrate the role of adipose mesenchymal stem cells (ASCs) in angiogenesis. The angiogenic mechanism has been ascribed to paracrine factors since these cells secrete a plenty of signal molecules and growth factors. Recently it has been suggested that besides soluble factors, extracellular vesicles (EVs) that include exosomes and microvesicles may play a major role in cell-to-cell communication. It has been shown that EVs are implicated in the angiogenic process. Results Herein we studied whether EVs released by ASCs may mediate the angiogenic activity of these cells. Our results demonstrated that ASC-derived EVs induced in vitro vessel-like structure formation by human microvascular endothelial cells (HMEC). EV-stimulated HMEC when injected subcutaneously within Matrigel in SCID mice formed vessels. Treatment of ASCs with platelet-derived growth factor (PDGF) stimulated the secretion of EVs, changed their protein composition and enhanced the angiogenic potential. At variance of EVs released in basal conditions, PDGF-EVs carried c-kit and SCF that played a role in angiogenesis as specific blocking antibodies inhibited in vitro vessel-like structure formation. The enhanced content of matrix metalloproteinases in PDGF-EVs may also account for their angiogenic activity. Conclusions Our findings indicate that EVs released by ASCs may contribute to the ASC-induced angiogenesis and suggest that PDGF may trigger the release of EVs with an enhanced angiogenic potential.
机译:背景几项研究证明了脂肪间充质干细胞(ASCs)在血管生成中的作用。血管生成机理归因于旁分泌因子,因为这些细胞分泌大量信号分子和生长因子。最近,有人提出,除可溶性因子外,包括外泌体和微囊泡的细胞外囊泡(EVs)可能在细胞间通讯中起主要作用。已经表明,EV与血管生成过程有关。结果本文研究了ASCs释放的EV是否可以介导这些细胞的血管生成活性。我们的结果证明,源自ASC的EVs通过人微血管内皮细胞(HMEC)诱导了体外血管样结构的形成。当皮下注射在SCID小鼠的Matrigel中时,EV刺激的HMEC形成血管。用血小板衍生的生长因子(PDGF)处理ASC刺激了EV的分泌,改变了它们的蛋白质组成并增强了血管生成的潜力。在基础条件下释放的EV中,PDGF-EV携带c-kit和SCF,它们在血管生成中起作用,因为特定的阻断抗体抑制了体外血管样结构的形成。 PDGF-EV中基质金属蛋白酶含量的增加也可能是其血管生成活性的原因。结论我们的发现表明ASC释放的EV可能有助于ASC诱导的血管生成,并提示PDGF可能触发具有增强的血管生成潜能的EV释放。

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