Department of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, University of Medicine and Dentistry of New Jersey, New Jersey Medical School, 185 South Orange Avenue, MSB G-609, Newark, NJ 07103, USA.
Cardiovasc Res. 2010 Jan 15;85(2):321-9. doi: 10.1093/cvr/cvp226. Epub 2009 Jul 3.
Activation of the ubiquitin-proteasome system has been described in different models of cardiac hypertrophy. Cardiac cell growth in response to pressure or volume overload, as well as physiological adaptive hypertrophy, is accompanied by an increase in protein ubiquitination, proteasome subunit expression, and proteasome activity. Importantly, an inhibition of proteasome activity prevents and reverses cardiac hypertrophy and remodelling in vivo. The focus of this review is to provide an update about the mechanisms by which proteasome inhibitors affect cardiac cell growth in adaptive and maladaptive models of cardiac hypertrophy. In the first part, we summarize how the proteasome affects both proteolysis and protein synthesis in a context of cardiac cell growth. In the second part, we show how proteasome inhibition can prevent and reverse cardiac hypertrophy and remodelling in response to different conditions of overload.
泛素-蛋白酶体系统的激活已在不同的心肌肥厚模型中被描述。心脏细胞在应对压力或容量超负荷以及生理性适应性肥厚时的生长伴随着蛋白泛素化、蛋白酶体亚基表达和蛋白酶体活性的增加。重要的是,蛋白酶体活性的抑制可预防和逆转体内的心肌肥厚和重构。本综述的重点是提供关于蛋白酶体抑制剂如何影响适应性和失调性心肌肥厚模型中心肌细胞生长的机制的最新信息。在第一部分中,我们总结了蛋白酶体如何在心脏细胞生长的背景下影响蛋白水解和蛋白质合成。在第二部分中,我们展示了蛋白酶体抑制如何预防和逆转不同超负荷条件下的心肌肥厚和重构。