Max-Delbrück-Center for Molecular Medicine, Cellular Neuroscience, 13092 Berlin, Germany.
Glia. 2010 Jul;58(9):1104-17. doi: 10.1002/glia.20991.
According to previously published ultrastructural studies, oligodendrocytes in white matter exhibit gap junctions with astrocytes, but not among each other, while in vitro oligodendrocytes form functional gap junctions. We have studied functional coupling among oligodendrocytes in acute slices of postnatal mouse corpus callosum. By whole-cell patch clamp we dialyzed oligodendrocytes with biocytin, a gap junction-permeable tracer. On average 61 cells were positive for biocytin detected by labeling with streptavidin-Cy3. About 77% of the coupled cells stained positively for the oligodendrocyte marker protein CNPase, 9% for the astrocyte marker GFAP and 14% were negative for both CNPase and GFAP. In the latter population, the majority expressed Olig2 and some NG2, markers for oligodendrocyte precursors. Oligodendrocytes are known to express Cx47, Cx32 and Cx29, astrocytes Cx43 and Cx30. In Cx47-deficient mice, the number of coupled cells was reduced by 80%. Deletion of Cx32 or Cx29 alone did not significantly reduce the number of coupled cells, but coupling was absent in Cx32/Cx47-double-deficient mice. Cx47-ablation completely abolished coupling of oligodendrocytes to astrocytes. In Cx43-deficient animals, oligodendrocyte-astrocyte coupling was still present, but coupling to oligodendrocyte precursors was not observed. In Cx43/Cx30-double deficient mice, oligodendrocyte-to-astrocyte coupling was almost absent. Uncoupled oligodendrocytes showed a higher input resistance. We conclude that oligodendrocytes in white matter form a functional syncytium predominantly among each other dependent on Cx47 and Cx32 expression, while astrocytic connexins expression can promote the size of this network.
根据之前发表的超微结构研究,白质中的少突胶质细胞与星形胶质细胞之间存在缝隙连接,但彼此之间不存在缝隙连接,而体外少突胶质细胞形成功能性缝隙连接。我们研究了出生后小鼠胼胝体急性切片中少突胶质细胞之间的功能偶联。通过全细胞膜片钳技术,我们用生物胞素(一种缝隙连接可通透的示踪剂)灌流少突胶质细胞。用链霉亲和素-Cy3 标记,平均有 61 个细胞呈生物胞素阳性。大约 77%的偶联细胞对少突胶质细胞标志物蛋白 CNPase 呈阳性染色,9%对星形胶质细胞标志物 GFAP 呈阳性染色,14%对 CNPase 和 GFAP 均呈阴性染色。在后一种细胞群中,大多数表达 Olig2 和一些 NG2,这是少突胶质前体细胞的标志物。已知少突胶质细胞表达 Cx47、Cx32 和 Cx29,星形胶质细胞表达 Cx43 和 Cx30。在 Cx47 缺陷型小鼠中,偶联细胞的数量减少了 80%。单独缺失 Cx32 或 Cx29 并不显著减少偶联细胞的数量,但在 Cx32/Cx47 双缺陷型小鼠中不存在偶联。Cx47 缺失完全消除了少突胶质细胞与星形胶质细胞的偶联。在 Cx43 缺陷型动物中,少突胶质细胞-星形胶质细胞偶联仍然存在,但没有观察到与少突胶质前体细胞的偶联。在 Cx43/Cx30 双缺陷型小鼠中,少突胶质细胞-星形胶质细胞偶联几乎不存在。未偶联的少突胶质细胞表现出更高的输入电阻。我们得出结论,白质中的少突胶质细胞主要通过 Cx47 和 Cx32 的表达形成功能性合胞体,而星形胶质细胞连接蛋白的表达可以促进这个网络的大小。