Institute of Molecular Oncology, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan.
Biochem Biophys Res Commun. 2010 Mar 26;394(1):106-11. doi: 10.1016/j.bbrc.2010.02.125. Epub 2010 Feb 23.
Barrier function of the epidermis is maintained by precise expression of keratinocyte-specific structural proteins to form the cornified cell envelope (CE). Loricrin, a major component of the CE, is expressed at the late stage of keratinocyte differentiation. In this study, we reveal the isoform-specific function of protein kinase C (PKC) in the regulation of loricrin expression. Both PKCdelta and PKCeta have been recognized as differentiation-promoting isoforms. However, loricrin expression was inversely controlled by PKCdelta and PKCeta in cultured keratinocytes and 3D skin culture; i.e. loricrin expression was decreased by PKCdelta and increased by PKCeta. To clarify the mechanisms that PKCdelta and PKCeta oppositely regulate the loricrin expression, we examined the expression of activator protein-1 (AP-1) family proteins, which modulate the transcription of loricrin and are downstream molecules of PKC. PKCdelta decreased c-Jun expression, whereas PKCeta increased JunD, which are positive regulators of loricrin transcription. These findings suggest that inverse effects of PKCdelta and PKCeta on loricrin expression attributes to the expression of c-Jun and JunD.
表皮的屏障功能是通过角质形成细胞特异性结构蛋白的精确表达来维持的,从而形成角蛋白细胞包膜(CE)。丝聚蛋白是 CE 的主要成分之一,在角质形成细胞分化的晚期表达。在本研究中,我们揭示了蛋白激酶 C(PKC)异构体在调节丝聚蛋白表达中的特异性功能。PKCδ和 PKCeta 都被认为是促进分化的异构体。然而,在培养的角质形成细胞和 3D 皮肤培养物中,PKCδ和 PKCeta 对丝聚蛋白表达的调控呈相反趋势;即 PKCδ降低丝聚蛋白的表达,而 PKCeta 增加丝聚蛋白的表达。为了阐明 PKCδ和 PKCeta 相反调节丝聚蛋白表达的机制,我们检查了激活蛋白-1(AP-1)家族蛋白的表达,这些蛋白调节丝聚蛋白的转录,是 PKC 的下游分子。PKCδ 降低 c-Jun 的表达,而 PKCeta 增加 JunD,它们是丝聚蛋白转录的正调节因子。这些发现表明,PKCδ 和 PKCeta 对丝聚蛋白表达的相反影响归因于 c-Jun 和 JunD 的表达。