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缝隙连接蛋白26和30在大鼠耳蜗中的表达。

Expression of the gap-junction connexins 26 and 30 in the rat cochlea.

作者信息

Lautermann J, ten Cate W J, Altenhoff P, Grümmer R, Traub O, Frank H, Jahnke K, Winterhager E

机构信息

Department of Otorhinolaryngology, University of Essen, Hufelandstrasse 55, D-45122 Essen, Germany.

出版信息

Cell Tissue Res. 1998 Dec;294(3):415-20. doi: 10.1007/s004410051192.

Abstract

Gap junction channels which are responsible for direct intercellular communication are composed of connexin proteins. Different connexins are distributed in a tissue-specific manner. Up to now only connexin26 has been identified to be widely expressed in the inner ear. In order to investigate the role of additional gap junction proteins, the expression of connexin30 and 43 was investigated in the rat cochlea. Connexin26 and connexin30 were both expressed in the spiral limbus, the spiral ligament, the stria vascularis and between supporting cells of the organ of Corti. Double-labeling experiments suggest that both connexins are partly colocalized between cells. Weak staining of connexin43 could only be detected in the stria vascularis, the spiral ligament and between organ of Corti supporting cells. The corresponding transcripts for connexin26, 30 and 43 could be detected by Northern blot analysis. The expression of different gap junction channels in the cochlea suggests functional diversity. Gap junctions in the inner ear may control ion concentrations of cochlear fluids or act as conduits through which glucose and other metabolites diffuse.

摘要

负责直接细胞间通讯的缝隙连接通道由连接蛋白组成。不同的连接蛋白以组织特异性方式分布。到目前为止,仅发现连接蛋白26在内耳中广泛表达。为了研究其他缝隙连接蛋白的作用,对大鼠耳蜗中连接蛋白30和43的表达进行了研究。连接蛋白26和连接蛋白30均在螺旋缘、螺旋韧带、血管纹以及柯蒂器支持细胞之间表达。双标记实验表明,两种连接蛋白在细胞间部分共定位。仅在血管纹、螺旋韧带以及柯蒂器支持细胞之间检测到连接蛋白43的弱染色。通过Northern印迹分析可检测到连接蛋白26、30和43的相应转录本。耳蜗中不同缝隙连接通道的表达表明其功能具有多样性。内耳中的缝隙连接可能控制耳蜗内液体的离子浓度,或作为葡萄糖和其他代谢物扩散的通道。

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