Tran Nhu Q, Crowe David L
Center for Craniofacial Molecular Biology, University of Southern California, 2250 Alcazar Street, Los Angeles, CA 90033, USA.
Biochem J. 2004 Jul 1;381(Pt 1):267-73. doi: 10.1042/BJ20031653.
Stratified squamous epithelial cells undergo an orderly process of terminal differentiation that is characterized by specific molecular and morphological changes, including expression of the cornified envelope protein involucrin. Significant progress has been made in characterizing the upstream regulatory region of the involucrin gene. Binding sites for AP-1 (activator protein 1) and Sp1 transcription factors were shown to be important for involucrin promoter activity and tissue-specific expression. Defective terminal differentiation is often characterized by decreased or lack of involucrin expression. Recently, a dominant-negative construct of the transcriptional co-activator P/CAF [p300/CBP-associated factor, where CBP stands for CREB (cAMP-response-element-binding protein)-binding protein] was shown to inhibit involucrin expression in immortalized keratinocytes [Kawabata, Kawahara, Kanekura, Araya, Daitoku, Hata, Miura, Fukamizu, Kanzaki, Maruyama and Nakajima (2002) J. Biol. Chem. 277, 8099-8105]. Loss of expression or inactivation of other co-activators has also been demonstrated [Suganuma, Kawabata, Ohshima, and Ikeda (2002) Proc. Natl. Acad. Sci. U.S.A. 99, 13073-13078]. In the present study, we re-expressed CBP and P/CAF in immortalized keratinocyte lines that had lost expression of these co-activator proteins. Re-expression of these proteins restored calcium- and RA (retinoic acid)-responsive involucrin expression in these cells. RA and calcium signalling induced exchange of CBP and P/CAF occupancy at the AP-1 sites of the involucrin promoter. CBP and P/CAF inductions of the involucrin expression were not dependent on MEK (mitogen-activated protein kinase/extracellular-signal-regulated kinase kinase), p38, protein kinase C or CaM kinase (calcium/calmodulin-dependent kinase) signalling. Kinase-induced changes in involucrin promoter activity directly resulted from changes in AP-1 protein expression. We concluded that CBP and P/CAF are important regulators of involucrin expression in stratified squamous epithelial cells.
复层鳞状上皮细胞经历一个有序的终末分化过程,其特征是特定的分子和形态学变化,包括角质化包膜蛋白内披蛋白的表达。在表征内披蛋白基因的上游调控区域方面已经取得了重大进展。已证明AP-1(激活蛋白1)和Sp1转录因子的结合位点对于内披蛋白启动子活性和组织特异性表达很重要。终末分化缺陷通常以内披蛋白表达减少或缺失为特征。最近,转录共激活因子P/CAF [p300/CBP相关因子,其中CBP代表CREB(cAMP反应元件结合蛋白)结合蛋白]的显性负性构建体被证明可抑制永生化角质形成细胞中的内披蛋白表达[河合、川原、金仓、荒谷、大德、羽田、三浦、深水、神崎、丸山和中岛(2002年)《生物化学杂志》277卷,8099 - 8105页]。其他共激活因子的表达缺失或失活也已得到证实[菅沼、河合、大岛和池田(2002年)《美国国家科学院院刊》99卷,13073 - 13078页]。在本研究中,我们在已失去这些共激活蛋白表达的永生化角质形成细胞系中重新表达了CBP和P/CAF。这些蛋白的重新表达恢复了这些细胞中对钙和视黄酸(RA)应答的内披蛋白表达。RA和钙信号诱导CBP和P/CAF在内披蛋白启动子的AP-1位点上的占据发生交换。CBP和P/CAF对内披蛋白表达的诱导不依赖于MEK(丝裂原活化蛋白激酶/细胞外信号调节激酶激酶)、p38、蛋白激酶C或CaM激酶(钙/钙调蛋白依赖性激酶)信号传导。激酶诱导的内披蛋白启动子活性变化直接源于AP-1蛋白表达的变化。我们得出结论,CBP和P/CAF是复层鳞状上皮细胞中内披蛋白表达的重要调节因子。