Concurrent Generation of Functional Smooth Muscle and Endothelial Cells via a Vascular Progenitor

被引:44
作者
Marchand, Melanie [1 ,2 ]
Anderson, Erica K. [1 ,2 ]
Phadnis, Smruti M. [1 ,2 ]
Longaker, Michael T. [3 ]
Cooke, John P. [4 ]
Chen, Bertha [2 ]
Pera, Renee A. Relijo [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Obstet & Gynecol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Surg, Hagey Lab Pediat Regenerat Med, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA 94305 USA
关键词
Stem cell; Embryonic stem cells; Endothelial cells; Smooth muscle cells; EMBRYONIC STEM-CELLS; NEOINTIMA FORMATION; DISEASE;
D O I
10.5966/sctm.2013-0124
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Smooth muscle cells (SMCs) and endothelial cells (ECs) are typically derived separately, with low efficiencies, from human pluripotent stem cells (hPSCs). The concurrent generation of these cell types might lead to potential applications in regenerative medicine to model, elucidate, and eventually treat vascular diseases. Here we report a robust two-step protocol that can be used to simultaneously generate large numbers of functional SMCs and ECs from a common proliferative vascular progenitor population via a two-dimensional culture system. We show here that coculturing hPSCs with OP9 cells in media supplemented with vascular endothelial growth factor, basic fibroblast growth factor, and bone morphogenetic protein 4 yields a higher percentage of CD31(+)CD34(+) cells on day 8 of differentiation. Upon exposure to endothelial differentiation media and SM differentiation media, these vascular progenitors were able to differentiate and mature into functional endothelial cells and smooth muscle cells, respectively. Furthermore, we were able to expand the intermediate population more than a billionfold to generate sufficient numbers of ECs and SMCs in parallel for potential therapeutic transplantations.
引用
收藏
页码:91 / 97
页数:7
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