Fan Guo-Chang, Chu Guoxiang, Kranias Evangelia G
Department of Pharmacology and Cell Biophysics, University of Cincinnati College of Medicine, 231 Albert Sabin Way, Cincinnati, OH 45267, USA.
Trends Cardiovasc Med. 2005 May;15(4):138-41. doi: 10.1016/j.tcm.2005.05.004.
The small heat shock protein Hsp20, also referred to as P20/HspB6, is expressed in the brain, stomach, liver, lung, kidney, blood, smooth muscle, skeletal muscle, and cardiac tissue. Although Hsp20 is not heat-inducible, several cellular signaling pathways appear to regulate its biologic functions. In recent years, tremendous advances have been made in elucidating the significance of Hsp20 in smooth muscle and its potential benefits on coronary vasculature. Of interest, recent findings have demonstrated that sustained beta-adrenergic stimulation results in expression and phosphorylation of cardiac Hsp20. Moreover, Hsp20 overexpression enhances cardiac function and renders cardioprotection against beta-agonist-mediated apoptosis and ischemia/reperfusion injury ex vivo and in vivo. This article reviews the new findings on translocation of Hsp20 in response to various stimuli and the multiple cellular targets of Hsp20, with special emphasis on its protective effects in the heart.
小分子热休克蛋白Hsp20,也被称为P20/HspB6,在脑、胃、肝脏、肺、肾、血液、平滑肌、骨骼肌和心脏组织中均有表达。尽管Hsp20不是热诱导型的,但几条细胞信号通路似乎可以调节其生物学功能。近年来,在阐明Hsp20在平滑肌中的意义及其对冠状血管系统的潜在益处方面取得了巨大进展。有趣的是,最近的研究结果表明,持续的β-肾上腺素能刺激会导致心脏Hsp20的表达和磷酸化。此外,Hsp20的过表达可增强心脏功能,并在体外和体内对β-激动剂介导的细胞凋亡以及缺血/再灌注损伤起到心脏保护作用。本文综述了Hsp20在各种刺激下易位的新发现以及Hsp20的多个细胞靶点,特别强调了其在心脏中的保护作用。