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了解转化生长因子-β信号通路在心脏中的作用:使用基因小鼠模型的研究综述

Understanding the role of transforming growth factor-beta signalling in the heart: overview of studies using genetic mouse models.

作者信息

Xiao Han, Zhang You-Yi

机构信息

Institute of Vascular Medicine, Peking University Third Hospital and Key Laboratory of Molecular Cardiovascular Sciences, Ministry of Education, Beijing, China.

出版信息

Clin Exp Pharmacol Physiol. 2008 Mar;35(3):335-41. doi: 10.1111/j.1440-1681.2007.04876.x.

Abstract
  1. In the present review, we focus on the genetic mouse models for transforming growth factor (TGF)-beta signalling, which have aided our understanding on the role of the TGF-beta signalling pathway in cardiac hypertrophy/fibrosis and the molecular mechanisms involved. 2. Knockout of TGF-beta is embryonic lethal, indicating that TGF-beta signalling plays an important role in embryonic development. In order to avoid this defect, many mouse strains with cardiac-specific targeted genes in TGF-beta signalling have been developed. 3. The TGF-beta family signalling pathway includes Smad-dependent and -independent pathways. 4. Investigations using the genetic mouse models have confirmed and uncovered the involvement of the TGF-beta/TGF-beta-activated kinase 1 (TAK1) pathway in the development of cardiac hypertrophy and fibrosis. Although the downstream cascade of TAK1-induced cardiac hypertrophy remains only partially defined, recent research indicates that the TGF-beta/TAK1/p38 pathway is involved in cardiac fibrosis 5. Smad-dependent signalling may not be involved in, or may even be inhibitory for, cardiac hypertrophy.
摘要
  1. 在本综述中,我们聚焦于转化生长因子(TGF)-β信号传导的基因小鼠模型,这些模型有助于我们理解TGF-β信号通路在心脏肥大/纤维化中的作用以及相关分子机制。2. TGF-β基因敲除会导致胚胎致死,这表明TGF-β信号传导在胚胎发育中起重要作用。为避免这一缺陷,已构建了许多在TGF-β信号传导中具有心脏特异性靶向基因的小鼠品系。3. TGF-β家族信号通路包括Smad依赖和非依赖途径。4. 使用基因小鼠模型的研究已证实并揭示了TGF-β/TGF-β激活激酶1(TAK1)途径参与心脏肥大和纤维化的发展。尽管TAK1诱导心脏肥大的下游级联反应仍仅部分明确,但最近的研究表明TGF-β/TAK1/p38途径参与心脏纤维化。5. Smad依赖的信号传导可能不参与心脏肥大,甚至可能对其具有抑制作用。

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