首页> 外文OA文献 >Expression of Kir4.1 and Kir5.1 inwardly rectifying potassium channels in oligodendrocytes, the myelinating cells of the CNS
【2h】

Expression of Kir4.1 and Kir5.1 inwardly rectifying potassium channels in oligodendrocytes, the myelinating cells of the CNS

机译:在少突胶质细胞(CNs的髓鞘细胞)中Kir4.1和Kir5.1向内整流钾通道的表达

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The inwardly rectifying K+ channel subtype Kir5.1 is only functional as a heteromeric channel with Kir4.1. In the CNS, Kir4.1 is localised to astrocytes and is the molecular basis of their strongly negative membrane potential. Oligodendrocytes are the specialised myelinating glia of the CNS and their resting membrane potential provides the driving force for ion and water transport that is essential for myelination. However, little is known about the ion channel profile of mature myelinating oligodendrocytes. Here, we identify for the first time colocalization of Kir5.1 with Kir4.1 in oligodendrocytes in white matter. Immunolocalization with membrane-bound Na+/K+-ATPase and western blot of the plasma membrane fraction of the optic nerve, a typical CNS white matter tract containing mainly axons and the oligodendrocytes that myelinate them, demonstrates that Kir4.1 and Kir5.1 are colocalized on oligodendrocyte cell membranes. Co-immunoprecipitation provides evidence that oligodendrocytes and astrocytes express a combination of homomeric Kir4.1 and heteromeric Kir4.1/Kir5.1 channels. Genetic knock-out and shRNA to ablate Kir4.1 indicates plasmalemmal expression of Kir5.1 in glia is largely dependent on Kir4.1 and the plasmalemmal anchoring protein PSD-95. The results demonstrate that, in addition to astrocytes, oligodendrocytes express both homomeric Kir4.1 and heteromeric Kir4.1/Kir5.1 channels. In astrocytes, these channels are essential to their key functions of K+ uptake and CO2/H+ chemosensation. We propose Kir4.1/Kir5.1 channels have equivalent functions in oligodendrocytes, maintaining myelin integrity in the face of large ionic shifts associated with action potential propagation along myelinated axons.
机译:向内整流的K +通道亚型Kir5.1仅与Kir4.1一起用作异聚通道。在CNS中,Kir4.1定位于星形胶质细胞,是其强烈负膜电位的分子基础。少突胶质细胞是中枢神经系统的特有的髓鞘胶质细胞,其静息膜电位为髓鞘形成所必需的离子和水传输提供了驱动力。然而,关于成熟的髓鞘少突胶质细胞的离子通道概况知之甚少。在这里,我们首次确定白质少突胶质细胞中Kir5.1与Kir4.1的共定位。用膜结合的Na + / K + -ATPase进行的免疫定位和视神经质膜部分的Western印迹,这是一个典型的CNS白质束,主要包含轴突和使它们脱髓鞘的少突胶质细胞,表明Kir4.1和Kir5.1是共定位的在少突胶质细胞细胞膜上。免疫共沉淀提供的证据表明,少突胶质细胞和星形胶质细胞表达同源的Kir4.1和异源的Kir4.1 / Kir5.1通道。基因敲除和shRNA消除Kir4.1表示胶质细胞中Kir5.1的血浆表达在很大程度上取决于Kir4.1和质膜锚定蛋白PSD-95。结果表明,除了星形胶质细胞,少突胶质细胞还表达同源的Kir4.1和异源的Kir4.1 / Kir5.1通道。在星形胶质细胞中,这些通道对于其摄取K +和CO2 / H +化学感受的关键功能至关重要。我们建议Kir4.1 / Kir5.1通道在少突胶质细胞中具有相同的功能,在与沿髓鞘轴突的动作电位传播相关的大离子位移的情况下,保持髓鞘完整性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号