School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, and Hunter Medical Research Institute, University of Newcastle, Callaghan, NSW 2308, Australia.
School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, and Hunter Medical Research Institute, University of Newcastle, Callaghan, NSW 2308, Australia.
Mol Cell Neurosci. 2017 Oct;84:119-131. doi: 10.1016/j.mcn.2017.01.005. Epub 2017 Jan 23.
The microtubule, F-actin and neurofilament networks play a critical role in neuronal cell morphogenesis, polarity and synaptic plasticity. Significantly, the assembly/disassembly and stability of these cytoskeletal networks is crucially modulated by protein phosphorylation and dephosphorylation events. Herein, we aim to more closely examine the role played by three major neuronal Ser/Thr protein phosphatases, PP2A, PP1 and calcineurin, in the homeostasis of the neuronal cytoskeleton. There is strong evidence that these enzymes interact with and dephosphorylate a variety of cytoskeletal proteins, resulting in major regulation of neuronal cytoskeletal dynamics. Conversely, we also discuss how multi-protein cytoskeletal scaffolds can also influence the regulation of these phosphatases, with important implications for neuronal signalling and homeostasis. Not surprisingly, deregulation of these cytoskeletal scaffolds and phosphatase dysfunction are associated with many neurological diseases.
微管、F-肌动蛋白和神经丝网络在神经元细胞形态发生、极性和突触可塑性中发挥着关键作用。重要的是,这些细胞骨架网络的组装/解组装和稳定性受到蛋白磷酸化和去磷酸化事件的严格调节。在此,我们旨在更仔细地研究三种主要的神经元丝氨酸/苏氨酸蛋白磷酸酶(PP2A、PP1 和钙调神经磷酸酶)在神经元细胞骨架稳态中的作用。有强有力的证据表明,这些酶与多种细胞骨架蛋白相互作用并使其去磷酸化,从而对神经元细胞骨架动力学进行主要调控。相反,我们还讨论了多蛋白细胞骨架支架如何影响这些磷酸酶的调节,这对神经元信号转导和稳态具有重要意义。毫不奇怪,这些细胞骨架支架的失调和磷酸酶功能障碍与许多神经疾病有关。