Charles A C, Naus C C, Zhu D, Kidder G M, Dirksen E R, Sanderson M J
Department of Neurology, UCLA School of Medicine 90024.
J Cell Biol. 1992 Jul;118(1):195-201. doi: 10.1083/jcb.118.1.195.
Calcium signaling in C6 glioma cells in culture was examined with digital fluorescence video microscopy. C6 cells express low levels of the gap junction protein connexin43 and have correspondingly weak gap junctional communication as evidenced by dye coupling (Naus, C. C. G., J. F. Bechberger, S. Caveney, and J. X. Wilson. 1991. Neurosci. Lett. 126:33-36). Transfection of C6 cells with the cDNA encoding connexin43 resulted in clones with increased expression of connexin43 mRNA and protein and increased dye coupling, as well as markedly reduced rates of proliferation (Zhu, D., S. Caveney, G. M. Kidder, and C. C. Naus. 1991. Proc. Natl. Acad. Sci. USA. 88:1883-1887; Naus, C. C. G., D. Zhu, S. Todd, and G. M. Kidder. 1992. Cell Mol. Neurobiol. 12:163-175). Mechanical stimulation of a single cell in a culture of non-transfected C6 cells induced a wave of increased intracellular calcium concentration ([Ca2+]i) that showed little or no communication to adjacent cells. By contrast, mechanical stimulation of a single cell in cultures of C6 clones expressing transfected connexin43 cDNA induced a Ca2+ wave that was communicated to multiple surrounding cells, and the extent of communication was proportional to the level of expression of the connexin43 cDNA. These results provide direct evidence that intercellular Ca2+ signaling occurs via gap junctions. Ca2+ signaling through gap junctions may provide a means for the coordinated regulation of cellular function, including cell growth and differentiation.
采用数字荧光视频显微镜对培养的C6胶质瘤细胞中的钙信号进行了检测。C6细胞表达低水平的缝隙连接蛋白连接蛋白43,相应地缝隙连接通讯也较弱,这一点通过染料偶联得到了证实(瑙斯,C.C.G.,J.F.贝奇伯格,S.卡维尼,以及J.X.威尔逊。1991年。《神经科学快报》126:33 - 36)。用编码连接蛋白43的cDNA转染C6细胞,产生了连接蛋白43 mRNA和蛋白表达增加、染料偶联增加以及增殖速率显著降低的克隆(朱,D.,S.卡维尼,G.M.基德,以及C.C.瑙斯。1991年。《美国国家科学院院刊》88:1883 - 1887;瑙斯,C.C.G.,D.朱,S.托德,以及G.M.基德。1992年。《细胞与分子神经生物学》12:163 - 175)。在未转染的C6细胞培养物中对单个细胞进行机械刺激,会诱导细胞内钙浓度([Ca2+]i)升高的波,该波与相邻细胞几乎没有或没有通讯。相比之下,在表达转染的连接蛋白43 cDNA的C6克隆培养物中对单个细胞进行机械刺激,会诱导一个Ca2+波,该波会传递给多个周围细胞,并且通讯程度与连接蛋白43 cDNA的表达水平成正比。这些结果提供了直接证据,表明细胞间Ca2+信号通过缝隙连接发生。通过缝隙连接的Ca2+信号可能为细胞功能的协调调节提供一种方式,包括细胞生长和分化。