TRANSFORMING GROWTH-FACTOR-BETA IN CARDIAC ONTOGENY AND ADAPTATION

被引:75
作者
MACLELLAN, WR
BRAND, T
SCHNEIDER, MD
机构
[1] BAYLOR COLL MED, MOLEC CARDIOL UNIT, 1 BAYLOR PLAZA, ROOM 506C, HOUSTON, TX 77030 USA
[2] BAYLOR COLL MED, DEPT MED, HOUSTON, TX 77030 USA
[3] BAYLOR COLL MED, DEPT CELL BIOL, HOUSTON, TX 77030 USA
[4] BAYLOR COLL MED, DEPT MOLEC PHYSIOL & BIOPHYS, HOUSTON, TX 77030 USA
关键词
TRANSFORMING GROWTH FACTOR-BETA; CARDIAC GENE EXPRESSION; HYPERTROPHY; DEVELOPMENT;
D O I
10.1161/01.RES.73.5.783
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The transforming growth factor-beta (TGF-beta) superfamily comprises a set of regulatory peptides with multiple effects on cell growth and differentiation. The elaborate regulation of TGF-betas during embryonic development of the heart, the upregulation of TGF-beta after hemodynamic stress, and the impact of TGF-beta on cardiac gene expression together imply a prominent functional role for this family of growth factors in cardiac organogenesis and hypertrophy. Basal and TGF-beta-induced expression of skeletal alpha-actin, one of several genes specifically associated with developing or hypertrophied myocardium, each are contingent on transcriptional activation by serum response factor. A truncated form of the type II TGF-beta receptor, created by deletion of the cytoplasmic kinase domain, acts as a dominant suppressor of TGF-beta signal transduction in cultured cardiac muscle cells and may provide a suitable means to establish the functions of TGF-beta in vivo.
引用
收藏
页码:783 / 791
页数:9
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