Transcriptional regulation of cardiac progenitor cell populations

被引:61
作者
Masino, AM
Gallardo, TD
Wilcox, CA
Olson, EN
Williams, RS
Garry, DJ
机构
[1] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Mol Biol, Dallas, TX 75390 USA
[3] Presbyterian Med Ctr, Dept Oncol, Dallas, TX USA
[4] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
关键词
cardiac development; gene array; progenitor cells; transcriptome; transgenic mice;
D O I
10.1161/01.RES.0000138302.02691.be
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Transcriptome-wide analysis of dynamically regulated progenitor cell populations has the potential to elucidate key aspects of cardiac development. The heart, as the first organ to develop in the mammal, is a technically challenging but clinically relevant target for study. To define the transcriptional program of the cardiac progenitor, we used a novel transgenic strategy and fluorescence-activated cell sorting to reliably label and isolate cardiac progenitors directly from mouse embryos. Pure populations of cardiac progenitor cells were isolated from the cardiac crescent and 2 subsequent stages of heart development: the linear heart tube and the looping heart. RNA was isolated from stage-specific cardiac progenitors and subjected to transcriptome analysis by oligonucleotide array hybridization. The cardiac transcriptional regulatory programs were compared with the molecular programs of age-matched noncardiac embryonic cells, embryonic stem cells, adult cardiomyocytes, and each other to identify sets of genes exhibiting differential expression in the cardiac progenitor cell population. These results define the transcriptional profile of mammalian cardiac progenitor cells and provide insight into the molecular regulation of the earliest periods of heart development.
引用
收藏
页码:389 / 397
页数:9
相关论文
共 51 条
[1]  
BALDWIN HS, 1994, DEVELOPMENT, V120, P2539
[2]   Loss of function of the Prx1 and Prx2 homeobox genes alters architecture of the great elastic arteries and ductus arteriosus [J].
Bergwerff, M ;
Gittenberger-de Groot, AC ;
Wisse, LJ ;
DeRuiter, MC ;
Wessels, A ;
Martin, JF ;
Olson, EN ;
Kern, MJ .
VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY, 2000, 436 (01) :12-19
[3]  
BETTENHAUSEN B, 1995, DEVELOPMENT, V121, P2407
[4]   EXPRESSION OF HOMEOBOX GENES MSX-1 (HOX-7) AND MSX-2 (HOX-8) DURING CARDIAC DEVELOPMENT IN THE CHICK [J].
CHANTHOMAS, PS ;
THOMPSON, RP ;
ROBERT, B ;
YACOUB, MH ;
BARTON, PJR .
DEVELOPMENTAL DYNAMICS, 1993, 197 (03) :203-216
[5]   The hemangioblast: A common progenitor of hematopoietic and endothelial cells [J].
Choi, K .
JOURNAL OF HEMATOTHERAPY & STEM CELL RESEARCH, 2002, 11 (01) :91-101
[6]   Lineage analysis of the hemangioblast as defined by FLK1 and SCL expression [J].
Chung, YS ;
Zhang, WJ ;
Arentson, E ;
Kingsley, PD ;
Palis, J ;
Choi, K .
DEVELOPMENT, 2002, 129 (23) :5511-5520
[7]   Mesoangioblasts - vascular progenitors for extravascular mesodermal tissues [J].
Cossu, G ;
Bianco, P .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2003, 13 (05) :537-542
[8]   Cell therapy - Renovating the heart [J].
Couzin, J ;
Vogel, G .
SCIENCE, 2004, 304 (5668) :192-194
[9]  
EDMONDSON DG, 1994, DEVELOPMENT, V120, P1251
[10]   Cardiac homeobox gene NKX2-5 mutations and congenital heart disease -: Associations with atrial septal defect and hypoplastic left heart syndrome [J].
Elliott, DA ;
Kirk, EP ;
Yeoh, T ;
Chandar, S ;
McKenzie, F ;
Taylor, P ;
Grossfeld, P ;
Fatkin, D ;
Jones, O ;
Hayes, P ;
Feneley, M ;
Harvey, RP .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2003, 41 (11) :2072-2076