Department of Animal Resource Sciences, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8657, Japan.
Cell Death Dis. 2011 May 19;2(5):e157. doi: 10.1038/cddis.2011.40.
To maintain epidermal homeostasis, the balance between keratinocyte proliferation and differentiation is tightly controlled. However, the molecular mechanisms underlying this balance remain unclear. In 3D organotypic coculture with mouse keratinocytes and fibroblasts, the thickness of stratified cell layers was prolonged, and growth arrest and terminal differentiation were delayed when PKCη-null keratinocytes were used. Re-expression of PKCη in PKCη-null keratinocytes restored stratified cell layer thickness, growth arrest and terminal differentiation. We show that in 3D cocultured PKCη-null keratinocytes, p27(Kip1) mRNA was downregulated, whereas JNK/c-Jun signaling was enhanced. Furthermore, inhibition of JNK/c-Jun signaling in PKCη-null keratinocytes led to upregulation of p27(Kip1) mRNA, and to thinner stratified cell layers. Collectively, our findings indicate that PKCη upregulates p27(Kip1) mRNA through suppression of JNK/c-Jun signaling. This results in promoting a proliferation to differentiation switch in keratinocytes.
为了维持表皮的内稳态,角质形成细胞的增殖和分化之间的平衡受到严格控制。然而,这种平衡的分子机制尚不清楚。在与小鼠角质形成细胞和成纤维细胞的 3D 器官型共培养中,当使用 PKCη 缺失的角质形成细胞时,分层细胞层的厚度延长,生长停滞和终末分化被延迟。在 PKCη 缺失的角质形成细胞中重新表达 PKCη 可恢复分层细胞层的厚度、生长停滞和终末分化。我们表明,在 3D 共培养的 PKCη 缺失的角质形成细胞中,p27(Kip1)mRNA 下调,而 JNK/c-Jun 信号增强。此外,在 PKCη 缺失的角质形成细胞中抑制 JNK/c-Jun 信号导致 p27(Kip1)mRNA 的上调,并导致分层细胞层变薄。总之,我们的研究结果表明,PKCη 通过抑制 JNK/c-Jun 信号而上调 p27(Kip1)mRNA,从而促进角质形成细胞的增殖到分化转换。