Vascular smooth muscle cell differentiation from human stem/progenitor cells

被引:16
|
作者
Steinbach, Sarah K. [1 ,2 ]
Husain, Mansoor [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ,9 ]
机构
[1] Toronto Gen Res Inst, McEwen Ctr Regenerat Med, 101 Coll St, Toronto, ON M5G 1L7, Canada
[2] Toronto Gen Res Inst, Div Expt Therapeut, 101 Coll St, Toronto, ON M5G 1L7, Canada
[3] Univ Toronto, Dept Med, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[4] Univ Toronto, Dept Physiol, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[5] Univ Toronto, Dept Lab Med, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[6] Univ Toronto, Dept Pathobiol, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[7] Univ Toronto, Heart & Stroke Richard Lewar Ctr Excellence, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[8] Univ Toronto, Ted Rogers Ctr Heart Res, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[9] Univ Hlth Network, Peter Munk Cardiac Ctr, 200 Elizabeth St, Toronto, ON M5G 2C4, Canada
基金
加拿大健康研究院;
关键词
Vascular smooth muscle cell; Embryonic stem cells; Induced pluripotent stem cells; Lateral plate mesoderm; Neural crest; Serum-free; Coronary; SKIN-DERIVED PRECURSORS; CARDIOVASCULAR PROGENITOR CELLS; MESENCHYMAL STEM-CELLS; NEURAL-CREST; CANINE ATHEROSCLEROSIS; PRIMITIVE STREAK; SECONDARY HEART; EXPRESSION; MOUSE; SPECIFICATION;
D O I
10.1016/j.ymeth.2015.12.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Transplantation of vascular smooth muscle cells (VSMCs) is a promising cellular therapy to promote angiogenesis and wound healing. However, VSMCs are derived from diverse embryonic sources which may influence their role in the development of vascular disease and in its therapeutic modulation. Despite progress in understanding the mechanisms of VSMC differentiation, there remains a shortage of robust methods for generating lineage-specific VSMCs from pluripotent and adult stem/progenitor cells in serum-free conditions. Here we describe a method for differentiating pluripotent stem cells, such as embryonic and induced pluripotent stem cells, as well as skin-derived precursors, into lateral plate-derived VSMCs including 'coronary-like' VSMCs and neural crest-derived VSMC, respectively. We believe this approach will have broad applications in modeling origin-specific disease vulnerability and in developing personalized cell-based vascular grafts for regenerative medicine. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:85 / 92
页数:8
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