Eiberger Jürgen, Kibschull Mark, Strenzke Nicola, Schober Andreas, Büssow Heinrich, Wessig Carsten, Djahed Sina, Reucher Harald, Koch Dirk Alex, Lautermann Jürgen, Moser Tobias, Winterhager Elke, Willecke Klaus
Institut für Genetik, Universität Bonn, Bonn, Germany.
Glia. 2006 Apr 15;53(6):601-11. doi: 10.1002/glia.20315.
Using newly generated transgenic mice in which the coding region of the connexin29 (Cx29) gene was replaced by the lacZ reporter gene, we confirmed previous immunochemical results that Cx29 is expressed in Schwann cells, oligodendrocytes and Bergmann glia cells. In addition, we detected lacZ/Cx29 in Schwann cells of the sciatic nerve and in particular of the spiral ganglion in the inner ear, as well as at low abundance in the stria vascularis. Furthermore, we found lacZ/Cx29 expression in nonmyelinating Schwann cells of the adrenal gland, in chondrocytes of intervertebral discs and the epiphysis of developing bones. Electron microscopic analyses of myelin sheaths in the central and peripheral nervous system of Cx29-deficient mice detected no abnormalities. The nerve conduction in the sciatic nerve of adult Cx29-deficient mice and the auditory brain stem response as well as visually evoked potentials in 4- to 10-week-old Cx29-deficient mice were not different from wild-type littermate controls. Thus, in contrast to connexin32 and connexin47, which are also expressed in myelinating cells, Cx29 does not contribute to the function of myelin in adult mice.
利用新生成的转基因小鼠,其中连接蛋白29(Cx29)基因的编码区被lacZ报告基因取代,我们证实了先前的免疫化学结果,即Cx29在雪旺细胞、少突胶质细胞和伯格曼胶质细胞中表达。此外,我们在坐骨神经的雪旺细胞中,特别是在内耳的螺旋神经节中检测到lacZ/Cx29,在血管纹中也有低丰度表达。此外,我们在肾上腺的无髓鞘雪旺细胞、椎间盘软骨细胞和发育中骨骼的骨骺中发现了lacZ/Cx29表达。对Cx29缺陷小鼠中枢和外周神经系统髓鞘的电子显微镜分析未发现异常。成年Cx29缺陷小鼠坐骨神经的神经传导以及4至10周龄Cx29缺陷小鼠的听觉脑干反应和视觉诱发电位与野生型同窝对照无差异。因此,与也在有髓鞘细胞中表达的连接蛋白32和连接蛋白47不同,Cx29对成年小鼠髓鞘的功能没有贡献。