Grimes C A, Jope R S
Department of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Sparks Center 1057, Birmingham, AL 35294-0017, USA.
Prog Neurobiol. 2001 Nov;65(4):391-426. doi: 10.1016/s0301-0082(01)00011-9.
Glycogen synthase kinase-3beta (GSK3beta) is a fascinating enzyme with an astoundingly diverse number of actions in intracellular signaling systems. GSK3beta activity is regulated by serine (inhibitory) and tyrosine (stimulatory) phosphorylation, by protein complex formation, and by its intracellular localization. GSK3beta phosphorylates and thereby regulates the functions of many metabolic, signaling, and structural proteins. Notable among the signaling proteins regulated by GSK3beta are the many transcription factors, including activator protein-1, cyclic AMP response element binding protein, heat shock factor-1, nuclear factor of activated T cells, Myc, beta-catenin, CCAAT/enhancer binding protein, and NFkappaB. Lithium, the primary therapeutic agent for bipolar mood disorder, is a selective inhibitor of GSK3beta. This raises the possibility that dysregulation of GSK3beta and its inhibition by lithium may contribute to the disorder and its treatment, respectively. GSK3beta has been linked to all of the primary abnormalities associated with Alzheimer's disease. These include interactions between GSK3beta and components of the plaque-producing amyloid system, the participation of GSK3beta in phosphorylating the microtubule-binding protein tau that may contribute to the formation of neurofibrillary tangles, and interactions of GSK3beta with presenilin and other Alzheimer's disease-associated proteins. GSK3beta also regulates cell survival, as it facilitates a variety of apoptotic mechanisms, and lithium provides protection from many insults. Thus, GSK3beta has a central role regulating neuronal plasticity, gene expression, and cell survival, and may be a key component of certain psychiatric and neurodegenerative diseases.
糖原合酶激酶-3β(GSK3β)是一种迷人的酶,在细胞内信号系统中具有数量惊人的多样作用。GSK3β的活性受丝氨酸(抑制性)和酪氨酸(刺激性)磷酸化、蛋白质复合物形成及其细胞内定位的调节。GSK3β磷酸化并由此调节许多代谢、信号和结构蛋白的功能。在受GSK3β调节的信号蛋白中,值得注意的是许多转录因子,包括激活蛋白-1、环磷酸腺苷反应元件结合蛋白、热休克因子-1、活化T细胞核因子、Myc、β-连环蛋白、CCAAT/增强子结合蛋白和核因子κB。锂是双相情感障碍的主要治疗药物,是GSK3β的选择性抑制剂。这就提出了一种可能性,即GSK3β的失调及其被锂抑制可能分别导致该疾病及其治疗。GSK3β与阿尔茨海默病相关的所有主要异常都有关联。这些包括GSK3β与产生斑块的淀粉样蛋白系统成分之间的相互作用、GSK3β参与磷酸化微管结合蛋白tau,这可能有助于神经原纤维缠结的形成,以及GSK3β与早老素和其他阿尔茨海默病相关蛋白的相互作用。GSK3β还调节细胞存活,因为它促进多种凋亡机制,而锂可提供免受多种损伤的保护。因此,GSK3β在调节神经元可塑性、基因表达和细胞存活方面具有核心作用,可能是某些精神疾病和神经退行性疾病的关键组成部分。