PDGF-A as an epicardial mitogen during heart development

被引:43
作者
Kang, Jione [1 ]
Gu, Ying [1 ]
Li, Peng [1 ]
Johnson, Betsy L. [1 ]
Sucov, Henry M. [1 ]
Thomas, Penny S. [1 ]
机构
[1] Univ So Calif, Keck Sch Med, Inst Med Genet, Los Angeles, CA 90033 USA
关键词
PDGF; epicardium; myocardium; heart development; mitogenic signaling;
D O I
10.1002/dvdy.21469
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
In the developing heart, reciprocal interactions between the epicardium. and myocardium drive further sublineage specification and ventricular chamber morphogenesis. Several observations suggest that the epicardium is a source of secreted factors that influence cardiomyocyte proliferation, and these factors may have other roles as well. However, the identity of these epicardial factors remains mostly unknown. We have identified platelet-derived growth factor-A (PDGF-A) as one of several mitogens expressed by the rat EMC epicardial cell line (epicardial mesothelial cells), by embryonic epicardium and myocardium during mouse heart development, and by adult epicardium. Expression of the cognate receptor gene Pdgfra was detected in the epicardium, although a low level of expression in myocardium could not be ruled out. To address the potential role of PDGF signaling in heart development, we mutated both PDGF receptor genes in the myocardial and mesodermal compartments of the heart; however, this did not result in an observable cardiac phenotype. This finding suggests that mesodermal PDGF signaling is not essential in heart development, although its role may be redundant with other signaling pathways. Indeed, our results demonstrate the presence of additional mitogens that may have such an overlapping role.
引用
收藏
页码:692 / 701
页数:10
相关论文
共 49 条
[1]   Insight into the physiological functions of PDGF through genetic studies in mice [J].
Betsholtz, C .
CYTOKINE & GROWTH FACTOR REVIEWS, 2004, 15 (04) :215-228
[2]   Endothelium-specific ablation of PDGFB leads to pericyte loss and glomerular, cardiac and placental abnormalities [J].
Bjarnegård, M ;
Enge, M ;
Norlin, J ;
Gustafsdottir, S ;
Fredriksson, S ;
Abramsson, A ;
Takemoto, M ;
Gustafsson, E ;
Fässler, R ;
Betsholtz, C .
DEVELOPMENT, 2004, 131 (08) :1847-1857
[3]   PDGF-A signaling is a critical event in lung alveolar myofibroblast development and alveogenesis [J].
Bostrom, H ;
Willetts, K ;
Pekny, M ;
Leveen, P ;
Lindahl, P ;
Hedstrand, H ;
Pekna, M ;
Hellstrom, M ;
GebreMedhin, S ;
Schalling, M ;
Nilsson, M ;
Kurland, S ;
Tornell, J ;
Heath, JK ;
Betsholtz, C .
CELL, 1996, 85 (06) :863-873
[4]   BMP10 is essential for maintaining cardiac growth during murine cardiogenesis [J].
Chen, HY ;
Shi, S ;
Acosta, L ;
Li, WM ;
Lu, J ;
Bao, SD ;
Chen, ZA ;
Yang, ZC ;
Schneider, MD ;
Chien, KR ;
Conway, SJ ;
Yoder, MC ;
Haneline, LS ;
Franco, D ;
Shou, WN .
DEVELOPMENT, 2004, 131 (09) :2219-2231
[5]   Epicardial induction of fetal cardiomyocyte proliferation via a retinoic acid-inducible trophic factor [J].
Chen, THP ;
Chang, TC ;
Kang, JO ;
Choudhary, B ;
Makita, T ;
Tran, CM ;
Burch, JBE ;
Eid, H ;
Sucov, HM .
DEVELOPMENTAL BIOLOGY, 2002, 250 (01) :198-207
[6]   VCAM-1 inhibits TGFβ stimulated epithelial-mesenchymal transfonnation by modulating Rho activity and stabilizing intercellular adhesion in epicardial mesothelial cells [J].
Dokic, Danijela ;
Dettman, Robert W. .
DEVELOPMENTAL BIOLOGY, 2006, 299 (02) :489-504
[7]   EPICARDIAL MESOTHELIAL CELLS SYNTHESIZE AND RELEASE ENDOTHELIN [J].
EID, H ;
DEBOLD, MLK ;
CHEN, JH ;
DEBOLD, AJ .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1994, 24 (05) :715-720
[8]   ROLE OF EPICARDIAL MESOTHELIAL CELLS IN THE MODIFICATION OF PHENOTYPE AND FUNCTION OF ADULT-RAT VENTRICULAR MYOCYTES IN PRIMARY COCULTURE [J].
EID, H ;
LARSON, DM ;
SPRINGHORN, JP ;
ATTAWIA, MA ;
NAYAK, RC ;
SMITH, TW ;
KELLY, RA .
CIRCULATION RESEARCH, 1992, 71 (01) :40-50
[9]   To erb-B or not to erb-B... - Neuregulin-1/ErbB signaling in heart development and function [J].
Garratt, Alistair N. .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2006, 41 (02) :215-218
[10]   Epicardial outgrowth inhibition leads to compensatory mesothelial outflow tract collar and abnormal cardiac septation and coronary formation [J].
Gittenberger-de Groot, AC ;
Peeters, MPFMV ;
Bergwerff, M ;
Mentink, MMT ;
Poelmann, RE .
CIRCULATION RESEARCH, 2000, 87 (11) :969-971