Assessing identity, phenotype, and fate of endothelial progenitor cells.
Assessing identity, phenotype, and fate of endothelial progenitor cells.
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评估内皮祖细胞的身份、表型和命运。
DOI:
10.1161/atvbaha.107.155960
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发表时间:
2008-09
期刊:
影响因子:
--
通讯作者:
Yoder MC
中科院分区:
文献类型:
--
作者:
Hirschi KK;Ingram DA;Yoder MC
the Asahara at al10 article, human CD34 expressing cells (15.7% enriched for CD34 expression) in adult peripheral blood were interrogated as putative EPCs via in vitro and in vivo assays. While determining some of the unique aspects of putative EPCs in vitro, Asahara et al10 reported that the cells adhered to fibronectin-coated dishes with greater frequency than to type 1 collagen coated dishes and displayed a spindle-shaped morphology. Of interest, the putative CD34 EPCs when cocultured with CD34 depleted mononuclear cells formed clusters of round cells centrally and sprouts of spindle-shaped cells at the periphery. The adherent putative EPCs expressed a variety of cell surface proteins typically expressed by human umbilical vein endothelial cells and expression of these markers increased over time in vitro. Further studies provided evidence of these putative EPCs (CD34 or vascular endothelial growth factor receptor 2 [Flk-1] cells enriched to 20%) localizing to areas of neovascularization when injected in vivo into nude mice with induced hindlimb ischemia. Thus, in one article Asahara et al10 brought forth concepts of circulating EPCs, in vitro observations of EPC behavior, in vivo migration of putative EPCs to sites of vascular injury, and the paradigm of postnatal vasculogenesis.