Generation of Functional Ventricular Heart Muscle from Mouse Ventricular Progenitor Cells

被引:152
作者
Domian, Ibrahim J. [1 ,2 ]
Chiravuri, Murali [1 ]
van der Meer, Peter [1 ,3 ]
Feinberg, Adam W. [4 ]
Shi, Xi [1 ]
Shao, Ying [1 ]
Wu, Sean M. [1 ,2 ]
Parker, Kevin Kit [2 ,4 ,5 ]
Chien, Kenneth R. [1 ,2 ,6 ]
机构
[1] Massachusetts Gen Hosp, Cardiovasc Res Ctr, Boston, MA 02114 USA
[2] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Cardiol, NL-9700 RB Groningen, Netherlands
[4] Harvard Univ, Sch Engn & Appl Sci, Dis Biophys Grp, Cambridge, MA 02138 USA
[5] Harvard Univ, Wyss Inst Biologically Inspired Engn, Boston, MA 02115 USA
[6] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
关键词
SMOOTH-MUSCLE; ISL1; DIFFERENTIATION; TRANSCRIPTION; EXPRESSION; MEF2C;
D O I
10.1126/science.1177350
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mammalian heart is formed from distinct sets of first and second heart field (FHF and SHF, respectively) progenitors. Although multipotent progenitors have previously been shown to give rise to cardiomyocytes, smooth muscle, and endothelial cells, the mechanism governing the generation of large numbers of differentiated progeny remains poorly understood. We have employed a two-colored fluorescent reporter system to isolate FHF and SHF progenitors from developing mouse embryos and embryonic stem cells. Genome-wide profiling of coding and noncoding transcripts revealed distinct molecular signatures of these progenitor populations. We further identify a committed ventricular progenitor cell in the Islet 1 lineage that is capable of limited in vitro expansion, differentiation, and assembly into functional ventricular muscle tissue, representing a combination of tissue engineering and stem cell biology.
引用
收藏
页码:426 / 429
页数:4
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