MRC-University of Glasgow Centre for Virus Research, School of Infection and Immunity, College of Medical Veterinary and Life Sciences, University of Glasgow, Garscube Estate, Glasgow G61 1QH, UK.
Translation Research Platform for Veterinary Biologicals, Chennai, Tamil Nadu, India.
J Cell Sci. 2023 Jun 1;136(11). doi: 10.1242/jcs.259984. Epub 2023 Jun 8.
Gap junction channels, composed of connexins, allow direct cell-to-cell communication. Connexin 43 (Cx43; also known as GJA1) is widely expressed in tissues, including the epidermis. In a previous study of human papillomavirus-positive cervical epithelial tumour cells, we identified Cx43 as a binding partner of the human homologue of Drosophila Discs large (Dlg1; also known as SAP97). Dlg1 is a member of the membrane associated-guanylate kinase (MAGUK) scaffolding protein family, which is known to control cell shape and polarity. Here, we show that Cx43 also interacts with Dlg1 in uninfected keratinocytes in vitro and in keratinocytes, dermal cells and adipocytes in normal human epidermis in vivo. Depletion of Dlg1 in keratinocytes did not alter Cx43 transcription but was associated with a reduction in Cx43 protein levels. Reduced Dlg1 levels in keratinocytes resulted in a reduction in Cx43 at the plasma membrane with a concomitant reduction in gap junctional intercellular communication and relocation of Cx43 to the Golgi compartment. Our data suggest a key role for Dlg1 in maintaining Cx43 at the plasma membrane in keratinocytes.
缝隙连接通道由连接蛋白构成,允许细胞间直接通讯。连接蛋白 43(Cx43;也称为 GJA1)广泛表达于组织中,包括表皮。在先前对人乳头瘤病毒阳性宫颈上皮肿瘤细胞的研究中,我们发现 Cx43 是果蝇 Discs large(Dlg1;也称为 SAP97)同源物与人的结合伴侣。Dlg1 是膜相关鸟苷酸激酶(MAGUK)支架蛋白家族的成员,该家族已知可控制细胞形状和极性。在这里,我们表明 Cx43 还可在体外未感染的角质形成细胞以及体内正常人类表皮中的角质形成细胞、真皮细胞和脂肪细胞中与 Dlg1 相互作用。角质形成细胞中 Dlg1 的耗竭不会改变 Cx43 的转录,但与 Cx43 蛋白水平的降低有关。角质形成细胞中 Dlg1 水平的降低导致质膜处 Cx43 的减少,同时伴随细胞间隙连接通讯的减少和 Cx43 向高尔基体区室的重新定位。我们的数据表明 Dlg1 在维持角质形成细胞中质膜处的 Cx43 方面起着关键作用。