Ben Zablah Youssif, Merovitch Neil, Jia Zhengping
Program in Neurosciences and Mental Health, The Hospital for Sick Children, Peter Gilgan Centre for Research and Learning, Toronto, ON, Canada.
Department of Physiology, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Front Cell Dev Biol. 2020 Nov 12;8:594998. doi: 10.3389/fcell.2020.594998. eCollection 2020.
Actin-depolymerization factor (ADF)/cofilin, a family of actin-binding proteins, are critical for the regulation of actin reorganization in response to various signals. Accumulating evidence indicates that ADF/cofilin also play important roles in neuronal structure and function, including long-term potentiation and depression. These are the most extensively studied forms of long-lasting synaptic plasticity and are widely regarded as cellular mechanisms underlying learning and memory. ADF/cofilin regulate synaptic function through their effects on dendritic spines and the trafficking of glutamate receptors, the principal mediator of excitatory synaptic transmission in vertebrates. Regulation of ADF/cofilin involves various signaling pathways converging on LIM domain kinases and slingshot phosphatases, which phosphorylate/inactivate and dephosphorylate/activate ADF/cofilin, respectively. Actin-depolymerization factor/cofilin activity is also regulated by other actin-binding proteins, activity-dependent subcellular distribution and protein translation. Abnormalities in ADF/cofilin have been associated with several neurodegenerative disorders such as Alzheimer's disease. Therefore, investigating the roles of ADF/cofilin in the brain is not only important for understanding the fundamental processes governing neuronal structure and function, but also may provide potential therapeutic strategies to treat brain disorders.
肌动蛋白解聚因子(ADF)/丝切蛋白是一类肌动蛋白结合蛋白,对于响应各种信号调节肌动蛋白重组至关重要。越来越多的证据表明,ADF/丝切蛋白在神经元结构和功能中也发挥着重要作用,包括长时程增强和长时程抑制。这些是研究最广泛的持久突触可塑性形式,被广泛认为是学习和记忆的细胞机制。ADF/丝切蛋白通过影响树突棘和谷氨酸受体的运输来调节突触功能,谷氨酸受体是脊椎动物兴奋性突触传递的主要介质。对ADF/丝切蛋白的调节涉及多种信号通路,这些信号通路汇聚于LIM结构域激酶和弹弓磷酸酶,它们分别使ADF/丝切蛋白磷酸化/失活和去磷酸化/激活。肌动蛋白解聚因子/丝切蛋白的活性也受其他肌动蛋白结合蛋白、活性依赖性亚细胞分布和蛋白质翻译的调节。ADF/丝切蛋白的异常与几种神经退行性疾病有关,如阿尔茨海默病。因此,研究ADF/丝切蛋白在大脑中的作用不仅对于理解控制神经元结构和功能的基本过程很重要,而且可能为治疗脑部疾病提供潜在的治疗策略。