Hall Gentzon, Hasday Jeffery D, Rogers Terry B
Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
J Mol Cell Cardiol. 2006 Oct;41(4):580-91. doi: 10.1016/j.yjmcc.2006.07.006. Epub 2006 Sep 1.
The Nuclear Factor-kappaB (NF-kappaB) signaling pathway has been linked to several pathologic processes in the myocardium including cardiomyocyte proinflammatory cytokine release, ischemia/reperfusion injury, hypertrophy and apoptosis. However, very little is known about the intracellular mechanisms that govern NF-kappaB activity in the myocardial cells. Recent advances in our understanding of the regulation of NF-kappaB signaling in non-myocyte systems suggest that the activity of the NF-kappaB pathway is tightly regulated by a diversity of stress-activated signaling intermediates through direct post-translational modification of various components of the NF-kappaB pathway. In this review, we will focus on these recent revelations and their implications not only in cardiac pathologies, but in the development of new therapeutic strategies to manage heart disease.
核因子-κB(NF-κB)信号通路与心肌中的多种病理过程相关,包括心肌细胞促炎细胞因子释放、缺血/再灌注损伤、肥大和凋亡。然而,对于心肌细胞中调控NF-κB活性的细胞内机制却知之甚少。我们对非心肌细胞系统中NF-κB信号调控的最新认识表明,NF-κB信号通路的活性通过对NF-κB通路各种组分的直接翻译后修饰,受到多种应激激活信号中间体的严格调控。在这篇综述中,我们将聚焦于这些最新发现及其不仅在心脏病理学方面,而且在开发治疗心脏病新策略方面的意义。