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Method for in vitro differentiation of bone marrow mesenchymal stem cells into endothelial progenitor cells and vascular endothelial cells

机译:骨髓间充质干细胞体外分化为内皮祖细胞和血管内皮细胞的方法

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摘要

Vascular development is a regulated process and is dependent on the participation and differentiation of many cell types including the proliferation and migration of vascular endothelial cells and differentiation of endothelial progenitor cells (EPCs) to mesodermal precursor cells. Thus, reconstitution of this process in vitro necessitates providing ambient conditions for generating and culturing EPCs in vitro and differentiating them to vascular endothelial cells. In the present study, we developed methods to differentiate bone marrow mesenchymal stem cells (MSC) into EPCs and to vascular endothelial cells. Bone marrow MSC from canines and human sources were differentiated in vitro in to EPCs. These EPCs were able to express a variety of endothelial markers following 7 days in culture. Further culturing led to the appearance of an increased number and proportion of endothelial cells. These cells were stable even after 30 generations in culture. There was a gradual loss of CD31 and increased expression of factor VIII, VEGFR and CD133. VEGF being highly angiogenic, helps in the vascular development. These results provide the basis for the possible development of vasculature in vitro conditions for biomedical applications and in vivo for organ/tissue reconstruction therapies.
机译:血管发育是受调节的过程,并且取决于许多细胞类型的参与和分化,包括血管内皮细胞的增殖和迁移以及内皮祖细胞(EPC)向中胚层前体细胞的分化。因此,在体外重建该过程必须提供用于在体外产生和培养EPC并将它们分化为血管内皮细胞的环境条件。在本研究中,我们开发了将骨髓间充质干细胞(MSC)分化为EPC和血管内皮细胞的方法。来自犬和人来源的骨髓MSC在体外分化为EPC。这些EPC在培养7天后能够表达多种内皮标记。进一步培养导致出现内皮细胞数量和比例增加。这些细胞即使在培养了30代后仍保持稳定。 CD31逐渐消失,VIII因子,VEGFR和CD133的表达增加。 VEGF具有高度血管生成作用,有助于血管发育。这些结果为生物医学应用的体外血管状况和器官/组织重建疗法的体内血管状况的可能发展提供了基础。

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