Edamura Mitsuhiro, Murakami Gen, Meng Hongrui, Itakura Makoto, Shigemoto Ryuichi, Fukuda Atsuo, Nakahara Daiichiro
Division of Psychology and Behavioral Neuroscience, Department of Integrated Human Sciences, Hamamatsu University School of Medicine, Higashi-ku, Hamamatsu, Japan.
Department of Biochemistry, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
PLoS One. 2014 Sep 30;9(9):e107099. doi: 10.1371/journal.pone.0107099. eCollection 2014.
Major histocompatibility complex class I (MHCI) molecules were recently identified as novel regulators of synaptic plasticity. These molecules are expressed in various brain areas, especially in regions undergoing activity-dependent synaptic plasticity, but their role in the nucleus accumbens (NAc) is unknown. In this study, we investigated the effects of genetic disruption of MHCI function, through deletion of β2-microblobulin, which causes lack of cell surface expression of MHCI. First, we confirmed that MHCI molecules are expressed in the NAc core in wild-type mice. Second, we performed electrophysiological recordings with NAc core slices from wild-type and β2-microglobulin knock-out mice lacking cell surface expression of MHCI. We found that low frequency stimulation induced long-term depression in wild-type but not knock-out mice, whereas high frequency stimulation induced long-term potentiation in both genotypes, with a larger magnitude in knock-out mice. Furthermore, we demonstrated that knock-out mice showed more persistent behavioral sensitization to cocaine, which is a NAc-related behavior. Using this model, we analyzed the density of total AMPA receptors and their subunits GluR1 and GluR2 in the NAc core, by SDS-digested freeze-fracture replica labeling. After repeated cocaine exposure, the density of GluR1 was increased, but there was no change in total AMPA receptors and GluR2 levels in wild-type mice. In contrast, following repeated cocaine exposure, increased densities of total AMPA receptors, GluR1 and GluR2 were observed in knock-out mice. These results indicate that functional deficiency of MHCI enhances synaptic potentiation, induced by electrical and pharmacological stimulation.
主要组织相容性复合体I类(MHCI)分子最近被鉴定为突触可塑性的新型调节因子。这些分子在大脑的各个区域表达,特别是在经历依赖活动的突触可塑性的区域,但它们在伏隔核(NAc)中的作用尚不清楚。在本研究中,我们通过缺失β2-微球蛋白来研究MHCI功能的基因破坏的影响,β2-微球蛋白的缺失会导致MHCI在细胞表面的表达缺失。首先,我们证实MHCI分子在野生型小鼠的NAc核心中表达。其次,我们对野生型和缺乏MHCI细胞表面表达的β2-微球蛋白基因敲除小鼠的NAc核心切片进行了电生理记录。我们发现低频刺激在野生型小鼠中诱导了长时程抑制,但在基因敲除小鼠中没有,而高频刺激在两种基因型中都诱导了长时程增强,在基因敲除小鼠中幅度更大。此外,我们证明基因敲除小鼠对可卡因表现出更持久的行为敏化,这是一种与NAc相关的行为。利用这个模型,我们通过SDS消化的冷冻断裂复制品标记分析了NAc核心中总AMPA受体及其亚基GluR1和GluR2的密度。反复接触可卡因后,野生型小鼠中GluR1的密度增加,但总AMPA受体和GluR2水平没有变化。相比之下,反复接触可卡因后,基因敲除小鼠中观察到总AMPA受体、GluR1和GluR2的密度增加。这些结果表明,MHCI的功能缺陷增强了由电刺激和药物刺激诱导的突触增强。