School of Biosciences, College of Life and Environmental Sciences, University of Birmingham, Edgbaston, UK.
J Cell Sci. 2012 Jul 1;125(Pt 13):3202-9. doi: 10.1242/jcs.101931. Epub 2012 Mar 27.
The human epidermis is a self-renewing, stratified epithelial tissue that provides the protective function of the skin. The principal cell type within the epidermis is the keratinocyte, and normal function of the epidermis requires that keratinocyte proliferation, differentiation and cell death be carefully controlled. There is clear evidence that signalling through adhesion receptors such as integrins and cadherins plays a key role in regulating epidermal function. Previous work has shown that Rho family GTPases regulate cadherin- and integrin-based adhesion structures and hence epidermal function. In this study, we show that a member of this family, Rnd3, regulates desmosomal cell-cell adhesion in that loss of Rnd3 expression leads to an increase in desmosomes at sites of cell-cell adhesion and altered colony morphology. Loss of Rnd3 expression is also associated with resistance to cisplatin-mediated apoptosis in keratinocytes and this resistance is mediated through the desmosomal protein plakoglobin. We propose a novel plakoglobin-dependent role for Rnd3 in the regulation of keratinocyte cell death.
人类表皮是一种自我更新的、分层的上皮组织,提供皮肤的保护功能。表皮中的主要细胞类型是角质形成细胞,表皮的正常功能要求角质形成细胞的增殖、分化和细胞死亡受到严格控制。有明确的证据表明,通过整合素和钙黏蛋白等粘附受体的信号转导在调节表皮功能方面起着关键作用。以前的工作表明,Rho 家族 GTPases 调节钙黏蛋白和整合素基粘附结构,从而调节表皮功能。在这项研究中,我们表明该家族的一个成员 Rnd3 调节桥粒的细胞-细胞粘附,因为 Rnd3 表达的缺失导致细胞-细胞粘附部位桥粒的增加和集落形态的改变。Rnd3 表达的缺失也与角质形成细胞对顺铂介导的细胞凋亡的抗性有关,这种抗性是通过桥粒蛋白桥粒蛋白来介导的。我们提出了一种新的桥粒蛋白依赖的 Rnd3 在调节角质形成细胞细胞死亡中的作用。