Mizuki Yutaka, Takaki Manabu, Sakamoto Shinji, Okamoto Sojiro, Kishimoto Makiko, Okahisa Yuko, Itoh Masahiko, Yamada Norihito
Department of Neuropsychiatry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama 700-8558, Japan.
Department of Biochemistry, Dokkyo Medical University School of Medicine, 880 Kitakobayashi, Mibu-machi, Shimotsuga-gun, Tochigi 321-0293, Japan.
Int J Mol Sci. 2016 Dec 29;18(1):67. doi: 10.3390/ijms18010067.
Disturbances of synaptic connectivity during perinatal and adolescent periods have been hypothesized to be related to the pathophysiology of schizophrenia. Rho guanine nucleotide exchange factor 11 (ARHGEF11) is a specific guanine nucleotide exchange factors (GEF) for RhoA, which is a critical regulator of actin cytoskeleton dynamics and organization of dendritic spines and inhibitor of spine maintenance. variants are reported to be associated with a higher risk for the onset of schizophrenia in a Japanese population; however, how ARHGEF11 contributes to the pathogenesis of schizophrenia in dendritic spines is unknown. Therefore, we first studied the distribution, binding, and function of ARHGEF11 in the dendritic spines of the rat cerebral cortex. After subcellular fractionation of the rat cerebral cortex, ARHGEF11 was detected with synaptophysin and post-synaptic density protein 95 (PSD-95) in the P2 fractions including synaptosomal fractions containing presynaptic and postsynaptic density proteins. Endogenous ARHGEF11 was coimmunoprecipitated with synaptophysin or PSD-95. In cortical primary neurons at 28 days in vitro, immunostaining revealed that ARHGEF11 located in the dendrites and dendritic spines and colocalized with PSD-95 and synaptophysin. Overexpression of exogenous ARHGEF11 significantly decreased the number of spines ( = 0.008). These results indicate that ARHGEF11 is likely to be associated with synaptic membranes and regulation of spine.
围产期和青春期突触连接的紊乱被认为与精神分裂症的病理生理学有关。Rho鸟嘌呤核苷酸交换因子11(ARHGEF11)是RhoA的特异性鸟嘌呤核苷酸交换因子(GEF),RhoA是肌动蛋白细胞骨架动力学和树突棘组织的关键调节因子,也是棘突维持的抑制剂。据报道,在日本人群中,该基因变体与精神分裂症发病风险较高有关;然而,ARHGEF11如何在树突棘中促成精神分裂症的发病机制尚不清楚。因此,我们首先研究了ARHGEF11在大鼠大脑皮质树突棘中的分布、结合和功能。对大鼠大脑皮质进行亚细胞分级分离后,在包含突触前和突触后密度蛋白的突触体分级分离的P2级分中,用突触素和突触后密度蛋白95(PSD - 95)检测到了ARHGEF11。内源性ARHGEF11与突触素或PSD - 95进行了共免疫沉淀。在体外培养28天的皮质原代神经元中,免疫染色显示ARHGEF11位于树突和树突棘中,并与PSD - 95和突触素共定位。外源性ARHGEF11的过表达显著减少了棘突数量(P = 0.008)。这些结果表明,ARHGEF11可能与突触膜及棘突调节有关。