Center for Translational Medicine and Cardiology Division, Thomas Jefferson University Hospital, Philadelphia, PA, USA.
J Mol Cell Cardiol. 2011 Oct;51(4):607-13. doi: 10.1016/j.yjmcc.2010.11.020. Epub 2010 Dec 13.
The GSK-3 family of serine/threonine kinases, which is comprised of two isoforms (α and β), was initially identified as a negative regulator of glycogen synthase, the rate limiting enzyme of glycogen synthesis [1,2]. In the 30 years since its initial discovery, the family has been reported to regulate a host of additional cellular processes and, consequently, disease states such as bipolar disorders, diabetes, inflammatory diseases, cancer, and neurodegenerative diseases including Alzheimer's Disease and Parkinson's Disease [3,4]. As a result, there has been intense interest on the part of the pharmaceutical industry in developing small molecule antagonists of GSK-3. Herein, we will review the roles played by GSK-3s in the heart, focusing primarily on recent studies that have employed global and tissue-specific gene deletion. We will highlight roles in various pathologic processes, including pressure overload and ischemic injury, focusing on some striking isoform-specific effects of the family. Due to space limitations and/or the relatively limited data in gene-targeted mice, we will not be addressing the family's roles in ischemic pre-conditioning or its many interactions with various pro- and anti-apoptotic factors. This article is part of a special issue entitled "Key Signaling Molecules in Hypertrophy and Heart Failure."
GSK-3 家族是丝氨酸/苏氨酸激酶家族,由两种同工酶(α和β)组成,最初被鉴定为糖原合酶的负调节剂,糖原合酶是糖原合成的限速酶[1,2]。自最初发现以来的 30 年中,该家族已被报道调节多种额外的细胞过程,因此会导致各种疾病状态,如双相情感障碍、糖尿病、炎症性疾病、癌症和神经退行性疾病,包括阿尔茨海默病和帕金森病[3,4]。因此,制药行业对开发 GSK-3 的小分子拮抗剂产生了浓厚的兴趣。本文将综述 GSK-3 在心脏中的作用,主要集中在最近使用全局和组织特异性基因缺失的研究。我们将重点介绍其在各种病理过程中的作用,包括压力超负荷和缺血性损伤,特别强调家族的一些显著的同工酶特异性效应。由于篇幅限制和/或基因靶向小鼠中相对有限的数据,我们将不讨论家族在缺血预适应中的作用及其与各种促凋亡和抗凋亡因子的许多相互作用。本文是题为“肥大和心力衰竭中的关键信号分子”的特刊的一部分。