Forde J E, Dale T C
Biomedical Sciences Building, Cardiff School of Biosciences, Museum Avenue, CF10 3US, Cardiff, UK.
Cell Mol Life Sci. 2007 Aug;64(15):1930-44. doi: 10.1007/s00018-007-7045-7.
The serine/threonine kinase glycogen synthase kinase-3 (GSK-3) was initially identified as a key regulator of insulin-dependent glycogen synthesis. GSK-3 was subsequently shown to function in a wide range of cellular processes including differentiation, growth, motility and apoptosis. Aberrant regulation of GSK-3 has been implicated in a range of human pathologies including Alzheimer's disease, non-insulin-dependent diabetes mellitus (NIDDM) and cancer. As a consequence, the regulation of GSK-3 and the therapeutic potential of GSK-3 inhibitors have become key areas of investigation. This review will focus on the mechanisms of GSK-3 regulation, with emphasis on modulation by upstream signals, control of substrate specificity and GSK-3 localisation. The details of these mechanisms will be discussed in the context of specific signalling pathways.
丝氨酸/苏氨酸激酶糖原合酶激酶-3(GSK-3)最初被鉴定为胰岛素依赖性糖原合成的关键调节因子。随后发现GSK-3在包括分化、生长、运动和凋亡在内的广泛细胞过程中发挥作用。GSK-3的异常调节与一系列人类疾病有关,包括阿尔茨海默病、非胰岛素依赖型糖尿病(NIDDM)和癌症。因此,GSK-3的调节以及GSK-3抑制剂的治疗潜力已成为关键的研究领域。本综述将重点关注GSK-3的调节机制,重点是上游信号的调节、底物特异性的控制和GSK-3的定位。这些机制的细节将在特定信号通路的背景下进行讨论。