Lohman F P, Gibbs S, Fischer D F, Borgstein A M, van de Putte P, Backendorf C
Laboratory of Molecular Genetics, Leiden Institute of Chemistry, The Netherlands.
Oncogene. 1997 Apr 3;14(13):1623-7. doi: 10.1038/sj.onc.1200974.
In stratifying cultures of human keratinocytes, expression of the proto-oncoprotein c-JUN and the small proline rich 2 (SPRR2) protein, a precursor of the cornified cell envelope, are inversely related. Whereas c-JUN is typically found in basal proliferating cells, SPRR2 is restricted to suprabasal differentiating layers. Malignant keratinocytes (derived from squamous cell carcinoma, SCC) have reduced sprr2 expression, consistent with their low potential to differentiate, and express c-jun at higher levels than normal keratinocytes. A direct relation between c-jun and sprr2 expression was shown in several ways: transient ectopic expression of c-jun inhibits sprr2a promoter activity in normal differentiating cells, whereas in malignant keratinocytes a dominant negative c-jun mutant restored at least partially both the low promoter activity and the expression of endogenous sprr2. These effects are mediated via a 134 bp promoter fragment which does not include the sprr2a AP-1 binding site. Interestingly, in an SCC cell line, constitutively expressing the dominant c-jun mutant, expression of the terminal differentiation marker involucrin is also strongly increased, suggesting that c-JUN is a general modulator of keratinocyte terminal differentiation rather than only affecting the expression of sprr2.
在人角质形成细胞的分层培养中,原癌蛋白c-JUN与富含脯氨酸的小分子蛋白2(SPRR2,角质化包膜的前体)的表达呈负相关。c-JUN通常存在于基底增殖细胞中,而SPRR2局限于基底上层的分化层。恶性角质形成细胞(源自鳞状细胞癌,SCC)的sprr2表达降低,这与其低分化潜能一致,并且其c-jun表达水平高于正常角质形成细胞。c-jun与sprr2表达之间的直接关系通过多种方式得以证明:c-jun的瞬时异位表达抑制正常分化细胞中sprr2a启动子的活性,而在恶性角质形成细胞中,显性负性c-jun突变体至少部分恢复了低启动子活性和内源性sprr2的表达。这些效应是通过一个134 bp的启动子片段介导的,该片段不包括sprr2a AP-1结合位点。有趣的是,在一个持续表达显性c-jun突变体的SCC细胞系中,终末分化标志物兜甲蛋白的表达也显著增加,这表明c-JUN是角质形成细胞终末分化的一般调节因子,而不仅仅影响sprr2的表达。