Ochalski P A, Frankenstein U N, Hertzberg E L, Nagy J I
Department of Physiology, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.
Neuroscience. 1997 Feb;76(3):931-45. doi: 10.1016/s0306-4522(96)00394-6.
Connexin-43 in relation to gap junctions between astrocytes and between other cell types in rat spinal cord was investigated immunohistochemically. In gray matter, connexin-43 was distributed thoughout all laminae, but was more concentrated in the substantia gelatinosa and around the central canal. Ultrastructurally, immunostaining was present in the cytoplasm of, and at gap junctions between, fine astrocytic processes, most of which ensheathed neuronal elements. In white matter, connexin-43 was localized to somata of fibrous astrocytes, their glial fibrillary acidic protein-positive processes running parallel to myelinated axons, and at gap junctions between these processes. Labelling was also evident in thick radially-directed astrocytic processes displaying pockets of staining near immunopositive gap junctions. Near the cord surface, staining was present in cell bodies of subpial astrocytes and at gap junctions between their tangential processes which formed most of the glia limitans. Radially-directed processes of subpial astrocytes formed symmetrically- and asymmetrically-labelled gap junctions with each other and extended fine branches into surrounding white matter where they made contact and often formed gap junctions with oligodendrocytic processes at the outer surface of myelinated fibres. Immunopositive astrocyte processes also made heterologous gap junctions with unstained oligodendrocyte cell bodies. Ependymal cells lining the central canal exhibited apical cytoplasmic labelling, as well as symmetrically-labelled gap junctions at their apices. Ependymal cells also formed asymmetrically-labelled gap junctions at which the junctional membranes of unlabelled cells, presumed to be tanycytes, were unstained. The results indicate the expression of connexins in addition to connexin-43 at asymmetrically-labelled gap junctions between some astrocytic processes, between astrocytes and oligodendrocytes and between some ependymal cells. The presence of gap junctions between astrocyte and oligodendrocyte processes at the outer surface of myelin suggests incorporation of the latter into the extensive gap junctionally-coupled astrocytic syncytium.
采用免疫组织化学方法研究了大鼠脊髓中星形胶质细胞之间以及与其他细胞类型之间缝隙连接相关的连接蛋白43。在灰质中,连接蛋白43分布于所有板层,但在胶状质和中央管周围更为集中。超微结构上,免疫染色出现在纤细星形胶质细胞突起的细胞质中及其缝隙连接处,其中大多数包裹着神经元成分。在白质中,连接蛋白43定位于纤维性星形胶质细胞的胞体、其与有髓轴突平行的胶质纤维酸性蛋白阳性突起以及这些突起之间的缝隙连接处。在沿径向走行的粗大星形胶质细胞突起中也有标记,在免疫阳性的缝隙连接处附近可见染色区。在脊髓表面附近,软膜下星形胶质细胞的胞体以及构成胶质界膜大部分的其切线状突起之间的缝隙连接处有染色。软膜下星形胶质细胞的沿径向走行的突起相互形成对称和不对称标记的缝隙连接,并向周围白质伸出细支,在那里它们与有髓纤维外表面的少突胶质细胞突起接触并常形成缝隙连接。免疫阳性的星形胶质细胞突起也与未染色的少突胶质细胞胞体形成异源性缝隙连接。衬于中央管的室管膜细胞在顶端细胞质有标记,其顶端还有对称标记的缝隙连接。室管膜细胞还形成不对称标记的缝隙连接,在这些连接处,推测为伸长细胞的未标记细胞的连接膜未染色。结果表明,除连接蛋白43外,在一些星形胶质细胞突起之间、星形胶质细胞与少突胶质细胞之间以及一些室管膜细胞之间的不对称标记的缝隙连接处还表达其他连接蛋白。髓鞘外表面星形胶质细胞和少突胶质细胞突起之间存在缝隙连接,提示后者融入了广泛的通过缝隙连接耦合的星形胶质细胞合体。