Okuyama R, Ogawa E, Nagoshi H, Yabuki M, Kurihara A, Terui T, Aiba S, Obinata M, Tagami H, Ikawa S
Department of Dermatology, Tohoku University, Graduate School of Medicine, Tohoku University, Aoba-ku, Sendai, Japan.
Oncogene. 2007 Jul 5;26(31):4478-88. doi: 10.1038/sj.onc.1210235. Epub 2007 Jan 22.
p53 homologue, p51/p63, predominantly expressed in keratinocyte stem cells, is indispensable for the formation of epidermis. Notch1, another such gene indispensable for the process, induces growth arrest and differentiation in keratinocytes. We found that exogenous expression of DeltaNp51B (DeltaNp63alpha), one of the isoforms of p51 specifically expressed in basal keratinocytes, blocked Notch 1-dependent growth arrest and differentiation in mouse keratinocytes by inhibiting p21 expression and maintaining integrins expression. Furthermore, DeltaNp51B by itself was found to have ability to induce expression of integrin alpha6beta4, which promotes attachment of basal cells to basal membrane thereby keeping the cells in immature state. Therefore, we conclude that DeltaNp51B expression warrants integrin expression even under the influence of Notch1 and that DeltaNp51B is a long-sought factor required to maintain basal cell keratinocytes immaturity by inhibiting Notch1 activity. We will postulate a plausible model explaining the maintenance of the squamous epithelium architectures as well as offering mechanistic explanations for pathological features of skin diseases, including cancers, psoriasis along with physiological wound healings.
p53 同源物 p51/p63 主要在角质形成干细胞中表达,对表皮形成至关重要。Notch1 是该过程中另一个不可或缺的基因,可诱导角质形成细胞生长停滞和分化。我们发现,在基底角质形成细胞中特异性表达的 p51 异构体之一 DeltaNp51B(DeltaNp63α)的外源性表达,通过抑制 p21 表达和维持整合素表达,阻断了小鼠角质形成细胞中 Notch1 依赖性生长停滞和分化。此外,发现 DeltaNp51B 自身具有诱导整合素α6β4 表达的能力,整合素α6β4 可促进基底细胞与基底膜的附着,从而使细胞保持不成熟状态。因此,我们得出结论,即使在 Notch1 的影响下,DeltaNp51B 的表达也能保证整合素的表达,并且 DeltaNp51B 是通过抑制 Notch1 活性来维持基底细胞角质形成细胞不成熟所长期寻求的因子。我们将提出一个合理的模型,解释鳞状上皮结构的维持,并为包括癌症、银屑病在内的皮肤疾病的病理特征以及生理性伤口愈合提供机理解释。