Molecular basis of physiological heart growth: fundamental concepts and new players

被引:414
作者
Maillet, Marjorie [1 ]
van Berlo, Jop H. [1 ]
Molkentin, Jeffery D. [1 ,2 ]
机构
[1] Univ Cincinnati, Cincinnati Childrens Hosp Med Ctr, Dept Pediat, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Cincinnati Childrens Hosp Med Ctr, Howard Hughes Med Inst, Cincinnati, OH 45229 USA
基金
美国国家卫生研究院;
关键词
PATHOLOGICAL CARDIAC-HYPERTROPHY; LEFT-VENTRICULAR HYPERTROPHY; GLYCOGEN-SYNTHASE KINASE-3-BETA; TRANSGENIC MICE; FACTOR-I; SIGNALING PATHWAY; PROTEIN-KINASE; FACTOR-B; MYOCARDIAL-CONTRACTILITY; PRESSURE-OVERLOAD;
D O I
10.1038/nrm3495
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The heart hypertrophies in response to developmental signals as well as increased workload. Although adult-onset hypertrophy can ultimately lead to disease, cardiac hypertrophy is not necessarily maladaptive and can even be beneficial. Progress has been made in our understanding of the structural and molecular characteristics of physiological cardiac hypertrophy, as well as of the endocrine effectors and associated signalling pathways that regulate it. Physiological hypertrophy is initiated by finite signals, which include growth hormones (such as thyroid hormone, insulin, insulin-like growth factor 1 and vascular endothelial growth factor) and mechanical forces that converge on a limited number of intracellular signalling pathways (such as PI3K, AKT, AMP-activated protein kinase and mTOR) to affect gene transcription, protein translation and metabolism. Harnessing adaptive signalling mediators to reinvigorate the diseased heart could have important medical ramifications.
引用
收藏
页码:38 / 48
页数:11
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