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在转基因小鼠中敲除Cx47会导致少突胶质细胞-星形胶质细胞缝隙连接处的MUPP1、ZONAB和多种连接蛋白缺失。

Ablation of Cx47 in transgenic mice leads to the loss of MUPP1, ZONAB and multiple connexins at oligodendrocyte-astrocyte gap junctions.

作者信息

Li Xinbo, Penes M, Odermatt B, Willecke K, Nagy J I

机构信息

Department of Physiology, Faculty of Medicine, University of Manitoba, Manitoba, Canada.

出版信息

Eur J Neurosci. 2008 Oct;28(8):1503-17. doi: 10.1111/j.1460-9568.2008.06431.x.

Abstract

Oligodendrocytes in CNS are linked to astrocytes by heterotypic gap junctions composed of Cx32 and Cx47 in oligodendrocytes and Cx30 and Cx43 in astrocytes. These gap junctions also harbour regulatory proteins, including ZO-1 and ZONAB. Here, we investigated the localization of multi-PDZ domain protein 1 (MUPP1) at these gap junctions and examined accessory proteins and connexins associated with oligodendrocytes in Cx47-knockout mice. In every CNS region tested, punctate immunolabelling for MUPP1 was found on all oligodendrocyte somata in wild-type mice. These MUPP1-positive puncta were colocalized with punctate labelling for oligodendrocytic Cx32 or Cx47, and with astrocytic Cx30 or Cx43 at oligodendrocyte-astrocyte (O/A) gap junctions, but were not found at astrocyte-astrocyte gap junctions. In Cx47-knockout mice, immunolabelling of MUPP1 and ZONAB was absent on oligodendrocytes, whereas some ZO-1-positive puncta remained. In Cx32-knockout mice, MUPP1 and ZONAB persisted at O/A gap junctions. The absence of Cx47 in Cx47-knockout mice was accompanied by a total loss of punctate labelling for Cx30, Cx32 and Cx43 on oligodendrocyte somata, and by a dramatic increase in immunolabelling for Cx32 along myelinated fibers. These results demonstrate MUPP1 at O/A gap junctions and Cx47-dependent targeting of connexins to the plasma membranes of oligodendrocyte somata. Further, it appears that deficits in myelination reported in Cx47-knockout mice may arise not only from a loss of Cx47 but also from the accompanied loss of gap junctions and their regulatory proteins at oligodendrocyte somata, and that loss of Cx47 may be partly compensated for by elevated levels of Cx32 along myelinated fibers.

摘要

中枢神经系统中的少突胶质细胞通过由少突胶质细胞中的Cx32和Cx47以及星形胶质细胞中的Cx30和Cx43组成的异型缝隙连接与星形胶质细胞相连。这些缝隙连接还含有调节蛋白,包括ZO-1和ZONAB。在此,我们研究了多PDZ结构域蛋白1(MUPP1)在这些缝隙连接处的定位,并检测了Cx47基因敲除小鼠中与少突胶质细胞相关的辅助蛋白和连接蛋白。在所有测试的中枢神经系统区域中,野生型小鼠的所有少突胶质细胞胞体上均发现了MUPP1的点状免疫标记。这些MUPP1阳性斑点与少突胶质细胞Cx32或Cx47的点状标记以及少突胶质细胞-星形胶质细胞(O/A)缝隙连接处的星形胶质细胞Cx30或Cx43共定位,但在星形胶质细胞-星形胶质细胞缝隙连接处未发现。在Cx47基因敲除小鼠中,少突胶质细胞上未检测到MUPP1和ZONAB的免疫标记,而一些ZO-1阳性斑点仍然存在。在Cx32基因敲除小鼠中,MUPP1和ZONAB在O/A缝隙连接处持续存在。Cx47基因敲除小鼠中Cx47的缺失伴随着少突胶质细胞胞体上Cx30、Cx32和Cx43点状标记的完全丧失,以及沿有髓纤维的Cx32免疫标记的显著增加。这些结果证明了MUPP1在O/A缝隙连接处的存在以及Cx47依赖的连接蛋白靶向少突胶质细胞胞体的质膜。此外,Cx47基因敲除小鼠中报道的髓鞘形成缺陷似乎不仅源于Cx47的缺失,还源于少突胶质细胞胞体上缝隙连接及其调节蛋白的伴随丧失,并且Cx47的缺失可能部分由沿有髓纤维的Cx32水平升高所补偿。

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