树突棘
肌动蛋白解聚因子
长时程增强
神经元肌动蛋白重塑
细胞生物学
肌动蛋白细胞骨架
生物
Profilin公司
神经科学
Rho相关蛋白激酶
岩石2
基因剔除小鼠
突触可塑性
神经传递
MDia1公司
肌动蛋白重塑
突触
海马结构
细胞骨架
激酶
受体
生物化学
细胞
作者
Zikai Zhou,Yanghong Meng,Suhail Asrar,Zarko Todorovski,Zhengping Jia
标识
DOI:10.1016/j.neuropharm.2008.07.031
摘要
The actin cytoskeleton is critically involved in the regulation of the dendritic spine and synaptic properties, but the molecular mechanisms underlying actin dynamics in neurons are poorly defined. We took genetic approaches to create and analyze knockout mice specifically lacking ROCK2, a protein kinase that directly interacts with and is activated by the Rho GTPases, the central mediator of actin reorganization. We demonstrated that while these knockout mice were normal in gross brain anatomy, they were impaired in both basal synaptic transmission and hippocampal long-term potentiation (LTP). Consistent with the electrophysiological deficits, the ROCK2 knockout neurons showed deficits in spine properties, synapse density, the actin cytoskeleton, and the actin-binding protein cofilin. These results indicate that ROCK2/cofilin signaling is critical in the regulation of neuronal actin, spine morphology and synaptic function.
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