Defining the earliest step of cardiovascular progenitor specification during embryonic stem cell differentiation

被引:113
作者
Bondue, Antoine [1 ]
Tannler, Simon [1 ]
Chiapparo, Giuseppe [1 ]
Chabab, Samira [1 ]
Ramialison, Mirana [2 ]
Paulissen, Catherine [1 ]
Beck, Benjamin [1 ]
Harvey, Richard [2 ,3 ]
Blanpain, Cedric [1 ]
机构
[1] Univ Libre Bruxelles, Inst Rech Interdisciplinaire Biol Humaine & Mol, B-1070 Brussels, Belgium
[2] Victor Chang Cardiac Res Inst, Darlinghurst, NSW 2010, Australia
[3] Univ New S Wales, Fac Med, Kensington, NSW 2052, Australia
基金
欧洲研究理事会;
关键词
2ND HEART FIELD; SMOOTH-MUSCLE; MESP1; EXPRESSION; ORIGINS; REGULATOR; LINEAGES; PROTEIN; FATE; ISL1;
D O I
10.1083/jcb.201007063
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
During embryonic development and embryonic stem cell (ESC) differentiation, the different cell lineages of the mature heart arise from two types of multipotent cardiovascular progenitors (MCPs), the first and second heart fields. A key question is whether these two MCP populations arise from differentiation of a common progenitor. In this paper, we engineered Mesp1-green fluorescent protein (GFP) ESCs to isolate early MCPs during ESC differentiation. Mesp1-GFP cells are strongly enriched for MCPs, presenting the ability to differentiate into multiple cardiovascular lineages from both heart fields in vitro and in vivo. Transcriptional profiling of Mesp1-GFP cells uncovered cell surface markers expressed by MCPs allowing their prospective isolation. Mesp1 is required for MCP specification and the expression of key cardiovascular transcription factors. Isl1 is expressed in a subset of early Mesp1-expressing cells independently of Mesp1 and acts together with Mesp1 to promote cardiovascular differentiation. Our study identifies the early MCPs residing at the top of the cellular hierarchy of cardiovascular lineages during ESC differentiation.
引用
收藏
页码:751 / 765
页数:15
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