INSERM U 895, Team 5 Physiopathology of germ cell control: genomic and non genomic mechanisms Centre Méditerranéen de Médecine Moléculaire, Nice, F-06204 Cedex 3, France.
Dev Biol. 2010 Oct 1;346(1):54-67. doi: 10.1016/j.ydbio.2010.07.014. Epub 2010 Jul 22.
In different epithelia, cell membranes contacting one another form intercellular junctional complexes including tight, adherens and gap junctions, which could mutually influence the expression of each other. We have here investigated the role of Cx43 in the control of adherens and tight junction proteins (N-cadherin, beta-catenin, occludin and ZO-1) by using conditional Sertoli cell knockout Cx43 (SCCx43KO(-/-)) transgenic mice and specific anti-Cx43 siRNA. Gap junction coupling and Cx43 levels were reduced in SCCx43KO(-/-) as compared to Wild-type testes. Ultrastructural analysis revealed disappearance of gap junctions, the presence of tight and adherens junctions and persistent integrity of the blood-testis barrier in SCCx43KO(-/-) testis. Occludin, N-cadherin and beta-catenin levels were enhanced in SCCx43KO(-/-) mice as compared to Wild-type animals whereas ZO-1 levels were reduced. Cx43 siRNA blocked gap junction functionality in Sertoli cells and altered tight and adherens protein levels. The Cx43 control of tight and adherens junctions appeared channel-dependent since gap junction blockers (glycyrrhetinic acid and oleamide) led to similar results. These data suggest that the control of spermatogenesis by Cx43 may be mediated through Sertoli cell Cx43 channels, which are required, not only in cell/cell communication between Sertoli and germ cells, but also in the regulation of other junctional proteins essential for the blood-testis barrier.
在不同的上皮细胞中,相互接触的细胞膜形成细胞间连接复合体,包括紧密连接、黏附连接和缝隙连接,它们可以相互影响彼此的表达。我们在这里使用条件性睾丸支持细胞 Cx43 敲除(SCCx43KO(-/-))转基因小鼠和特异性抗 Cx43 siRNA 研究了 Cx43 对黏附连接和紧密连接蛋白(N-钙黏蛋白、β-连环蛋白、occludin 和 ZO-1)的控制作用。与野生型睾丸相比,SCCx43KO(-/-)睾丸中的缝隙连接偶联和 Cx43 水平降低。超微结构分析显示,SCCx43KO(-/-)睾丸中缝隙连接消失,存在紧密连接和黏附连接,血睾屏障保持完整。与野生型动物相比,SCCx43KO(-/-)小鼠中的 occludin、N-钙黏蛋白和β-连环蛋白水平升高,而 ZO-1 水平降低。Cx43 siRNA 阻断了睾丸支持细胞中的缝隙连接功能,并改变了紧密连接和黏附连接蛋白的水平。Cx43 对紧密连接和黏附连接的控制似乎依赖于通道,因为缝隙连接阻滞剂(甘草次酸和油酰胺)也导致了类似的结果。这些数据表明,Cx43 对精子发生的控制可能是通过 Cx43 通道介导的,这些通道不仅在睾丸支持细胞和生殖细胞之间的细胞/细胞通讯中是必需的,而且在调节血睾屏障所必需的其他连接蛋白中也是必需的。