首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Characterization of the AMPA-activated receptors present on motoneurons.
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Characterization of the AMPA-activated receptors present on motoneurons.

机译:表征运动神经元上AMPA激活的受体。

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摘要

Motoneurons have been shown to be particularly sensitive to Ca2+-dependent glutamate excitotoxicity, mediated via AMPA receptors (AMPARs). To determine the molecular basis for this susceptibility we have used immunocytochemistry, RT-PCR, and electrophysiology to profile AMPARs on embryonic day 14.5 rat motoneurons. Motoneurons show detectable AMPAR-mediated calcium permeability in vitro and in vivo as determined by cobalt uptake and electrophysiology. Motoneurons express all four AMPAR subunit mRNAs, with glutamate receptor (GluR) 2 being the most abundant (63.9+/-4.8%). GluR2 is present almost exclusively in the edited form, and electrophysiology confirms that most AMPARs present are calcium-impermeant. However, the kainate current in motoneurons was blocked an average of 32.0% by Joro spider toxin, indicating that a subset of the AM PARs is Ca2+-permeable. Therefore, heterogeneity of AMPARs, rather than the absence of GluR2 or the presence of unedited GluR2, explains AMPAR-mediated Ca2+ permeability. The relative levels of flip/flop isoforms of each subunit were also examined by semiquantitative PCR. Both isoforms were present, but the relative proportion varied for each subunit, and the flip isoform predominated. Thus, our data show that despite high levels of edited GluR2 mRNA, some AMPARs are Ca2+-permeable, and this subset of AMPARs can account for the AMPAR-mediated Ca2+ inflow inferred from cobalt uptake and electrophysiology studies.
机译:业已证明,单质子对通过AMPA受体(AMPAR)介导的Ca2 +依赖性谷氨酸兴奋性毒性特别敏感。为了确定这种敏感性的分子基础,我们使用了免疫细胞化学,RT-PCR和电​​生理学对胚胎第14.5天大鼠运动神经元的AMPAR进行了分析。由钴摄取和电生理学测定,单质子在体外和体内显示出可检测的AMPAR介导的钙渗透性。绒膜隆表达所有四个AMPAR亚基mRNA,其中谷氨酸受体(GluR)2含量最高(63.9 +/- 4.8%)。 GluR2几乎仅以编辑形式存在,并且电生理学证实存在的大多数AMPAR都是不渗透钙的。然而,运动神经元中的海藻酸盐电流被Joro蜘蛛毒素平均阻断了32.0%,这表明AM PAR的一个子集可渗透Ca2 +。因此,AMPAR的异质性而不是不存在GluR2或未编辑的GluR2的存在解释了AMPAR介导的Ca2 +渗透性。还通过半定量PCR检查了每个亚基的翻转/翻转同种型的相对水平。两种同工型都存在,但相对比例因每个亚基而异,而翻转型同工型占主导。因此,我们的数据表明,尽管GluR2 mRNA的编辑水平很高,但某些AMPAR仍可渗透Ca2 +,而这部分AMPAR可以解释由钴吸收和电生理研究推断出的AMPAR介导的Ca2 +流入。

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