Swenson K I, Jordan J R, Beyer E C, Paul D L
Department of Anatomy and Cellular Biology, Harvard Medical School, Boston, Massachusetts 02115.
Cell. 1989 Apr 7;57(1):145-55. doi: 10.1016/0092-8674(89)90180-3.
RNAs coding for connexins 32, 43, and the putative lens gap junction protein MP26 were tested for their ability to induce cell-cell coupling in Xenopus oocyte pairs. Large, voltage-insensitive conductances developed when connexin32 and 43 RNA-injected oocytes were paired both with themselves and with each other. Oocyte pairs injected with water manifested small conductances, which were symmetrically voltage-dependent. MP26 RNA-injected pairs displayed no conductances above control values. Unexpectedly, connexin43/water oocyte pairs developed high, asymmetrically voltage-dependent conductances, a property not displayed by the connexin32/water pairs. In single oocytes, these proteins remained intracellular until pairing, at which time the connexins, but not MP26, concentrated at the appositional areas.
对编码连接蛋白32、43以及假定的晶状体间隙连接蛋白MP26的RNA进行了测试,以检测它们在非洲爪蟾卵母细胞对中诱导细胞间偶联的能力。当注射连接蛋白32和43 RNA的卵母细胞自身配对以及相互配对时,会形成大的、电压不敏感的电导。注射水的卵母细胞对表现出小的电导,其呈对称的电压依赖性。注射MP26 RNA的卵母细胞对未显示出高于对照值的电导。出乎意料的是,连接蛋白43/水的卵母细胞对形成了高的、不对称电压依赖性电导,而连接蛋白32/水的卵母细胞对未表现出这种特性。在单个卵母细胞中,这些蛋白质在配对前一直保持在细胞内,此时连接蛋白而非MP26集中在相邻区域。