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脊髓少突胶质细胞之间的染料偶联:灰质和白质之间偶联效率的差异。

Dye coupling between spinal cord oligodendrocytes: differences in coupling efficiency between gray and white matter.

作者信息

Pastor A, Kremer M, Möller T, Kettenmann H, Dermietzel R

机构信息

Max Delbrück Center for Molecular Medicine, Berlin-Buch, Germany.

出版信息

Glia. 1998 Sep;24(1):108-20.

PMID:9700494
Abstract

Oligodendrocytes express two gap junction proteins, connexin32 (Cx32) and Cx45. To test for functional coupling between oligodendrocytes, cells were filled with the (Cx32-permeable) dyes Lucifer Yellow (LY) and Neurobiotin. Cells in slices from rat spinal cord were dialyzed via the patch pipette containing the dye while recording with the patch-clamp technique. The dye-labeled cells were identified as oligodendrocytes by their characteristic pattern of membrane currents and by morphology. In gray matter, 18% of the injected cells (N = 94) were coupled to more than three adjacent cells (slices from postnatal day 1 to 19). In contrast, in white matter, the dye was restricted to the injected cell (N = 63 for Lucifer Yellow injection only; N = 11 for LY and Neurobiotin) indicating a lack of functional coupling. Immunolabeling of Cx32 in mature oligodendrocytes of white matter revealed that the gap junction protein is localized on the cell bodies and abaxonal processes which occupy non-overlapping territories. In immature white matter and gray matter, Cx32 is mostly concentrated in the somatic region of the cells. In addition to Cx32, we have obtained immunocytochemical data that oligodendrocytes can express Cx45 with a labeling pattern different from the Cx32 expression. Two alternative interpretations of the coupling data are discussed: 1) that the presence of Cx32 in mature white matter oligodendrocytes does not serve for communication between cells, but rather for communication within oligodendrocytes in the sense of autocellular coupling, or 2) that the glial syncytium is furnished with a high degree of functional rectification at the oligodendrocytic side.

摘要

少突胶质细胞表达两种间隙连接蛋白,即连接蛋白32(Cx32)和Cx45。为了检测少突胶质细胞之间的功能偶联,将细胞用(Cx32可通透的)染料鲁米诺黄(LY)和神经生物素填充。在使用膜片钳技术记录的同时,通过含有染料的膜片吸管对来自大鼠脊髓切片中的细胞进行透析。通过其特征性的膜电流模式和形态学,将染料标记的细胞鉴定为少突胶质细胞。在灰质中,18%的注入细胞(N = 94)与三个以上相邻细胞偶联(出生后第1天至19天的切片)。相比之下,在白质中,染料局限于注入的细胞(仅LY注射时N = 63;LY和神经生物素注射时N = 11),表明缺乏功能偶联。对白质成熟少突胶质细胞中Cx32的免疫标记显示,间隙连接蛋白定位于占据不重叠区域的细胞体和轴突下突起上。在未成熟的白质和灰质中,Cx32大多集中在细胞的胞体区域。除了Cx32,我们还获得了免疫细胞化学数据,即少突胶质细胞可以表达Cx45,其标记模式与Cx32的表达不同。讨论了偶联数据的两种不同解释:1)成熟白质少突胶质细胞中Cx32的存在并非用于细胞间通讯,而是用于自细胞偶联意义上的少突胶质细胞内通讯,或者2)胶质细胞合体在少突胶质细胞一侧具有高度的功能整流。

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