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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >AMPA glutamate receptor-mediated calcium signaling is transiently enhanced during development of oligodendrocytes.
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AMPA glutamate receptor-mediated calcium signaling is transiently enhanced during development of oligodendrocytes.

机译:在少突胶质细胞发育过程中,AMPA谷氨酸受体介导的钙信号传导暂时增强。

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摘要

Cells of the oligodendroglial lineage express Ca2+-permeable alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate-preferring glutamate receptors (AMPA-GluR) during development. Prolonged activation of their AMPA-GluR causes Ca2+ overload, resulting in excitotoxic death. Prior studies have shown that oligodendroglial progenitors and immature oligodendrocytes are susceptible to excitotoxicity, whereas mature oligodendrocytes are resistant. An unresolved issue has been why Ca2+-permeability of AMPA-GluR varies so markedly with oligodendroglial development, although the level of expression of edited GluR2, an AMPA-GluR subunit which blocks Ca2+ entry, is relatively constant. To address this question, we performed Ca2+ imaging, molecular and electrophysiological analyses using purified cultures of the rat oligodendroglial lineage. We demonstrate that transient up-regulation of expression of GluR3 and GluR4 subunits in oligodendroglial progenitors and immature oligodendrocytes results in the assembly by these cells, but not by oligodendroglial pre-progenitors or mature oligodendrocytes, of a population of AMPA-GluR which lack GluR2. This stage-specific up-regulation of edited GluR2-free, and hence Ca2+-permeable, AMPA-GluR explains the selective susceptibility to excitotoxicity of cells at these stages of oligodendroglial differentiation, and is likely to be important to these cells in the trans-synaptic Ca2+-signaling from glutamatergic neurons, which occurs in hippocampus
机译:少突胶质细胞系的细胞在发育过程中表达Ca2 +可渗透的α-氨基-3-羟基-5-甲基-4-异恶唑丙酸酯偏爱的谷氨酸受体(AMPA-GluR)。他们的AMPA-GluR的长时间激活会导致Ca2 +超载,从而导致兴奋性毒性死亡。先前的研究表明,少突胶质祖细胞和不成熟的少突胶质细胞对兴奋性中毒敏感,而成熟的少突胶质细胞具有抗性。一个尚未解决的问题是,为什么AMPA-GluR的Ca2 +渗透性会随着少突胶质细胞的发育而显着变化,尽管编辑后的GluR2(一种阻止Ca2 +进入的AMPA-GluR亚基)的表达水平相对恒定。为了解决这个问题,我们使用大鼠少突神经胶质谱系的纯化培养物进行了Ca2 +成像,分子和电生理分析。我们证明,少突胶质祖细胞和不成熟的少突胶质细胞中GluR3和GluR4亚基表达的瞬时上调会导致这些细胞而不是少突胶质前祖细胞或成熟的少突胶质细胞缺乏AMlu-GluR2的组装。编辑后的不含GluR2且因此具有Ca2 +渗透性的AMPA-GluR的这一阶段特异性上调解释了少突胶质细胞分化这些阶段细胞对兴奋性毒性的选择性敏感性,并且可能对这些细胞的反式-重要来自海马区的谷氨酸能神经元的突触Ca2 +信号传导

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