The Hippo pathway in the heart: pivotal roles in development, disease, and regeneration

被引:283
作者
Wang, Jun [1 ]
Liu, Shijie [2 ]
Heallen, Todd [2 ]
Martin, James F. [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Mol Physiol & Biophys, Houston, TX 77030 USA
[2] Texas Heart Inst, Cardiomyocyte Renewal Lab, Houston, TX 77025 USA
关键词
YES-ASSOCIATED PROTEIN; STROKE STATISTICS-2010 UPDATE; TRANSCRIPTION FACTORS MEDIATE; TGF-BETA; CARDIOMYOCYTE PROLIFERATION; TUMOR-SUPPRESSOR; CARDIAC DYSFUNCTION; CELL-PROLIFERATION; SIGNALING PATHWAY; ACTS DOWNSTREAM;
D O I
10.1038/s41569-018-0063-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Hippo-YAP (Yes-associated protein) pathway is an evolutionarily and functionally conserved regulator of organ size and growth with crucial roles in cell proliferation, apoptosis, and differentiation. This pathway has great potential for therapeutic manipulation in different disease states and to promote organ regeneration. In this Review, we summarize findings from the past decade revealing the function and regulation of the Hippo-YAP pathway in cardiac development, growth, homeostasis, disease, and regeneration. In particular, we highlight the roles of the Hippo-YAP pathway in endogenous heart muscle renewal, including the pivotal role of the Hippo-YAP pathway in regulating cardiomyocyte proliferation and differentiation, stress response, and mechanical signalling. The human heart lacks the capacity to self-repair; therefore, the loss of cardiomyocytes after injury such as myocardial infarction can result in heart failure and death. Despite substantial advances in the treatment of heart failure, an enormous unmet clinical need exists for alternative treatment options. Targeting the Hippo-YAP pathway has tremendous potential for developing therapeutic strategies for cardiac repair and regeneration for currently intractable cardiovascular diseases such as heart failure. The lessons learned from cardiac repair and regeneration studies will also bring new insights into the regeneration of other tissues with limited regenerative capacity.
引用
收藏
页码:672 / 684
页数:13
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