Fisher G J, Reddy A P, Datta S C, Kang S, Yi J Y, Chambon P, Voorhees J J
Department of Dermatology, University of Michigan Medical Center, Ann Arbor, USA.
J Invest Dermatol. 1995 Jul;105(1):80-6. doi: 10.1111/1523-1747.ep12313352.
We examined the regulation of cellular retinol-binding protein (CRBP) mRNA and protein expression in human skin in vivo by all-trans retinoic acid and all-trans retinol. Treatment of human skin for 24 h with all-trans retinoic acid (0.1%) or all-trans retinol (1.6%) induced CRBP mRNA 5.5-fold (p < 0.01, n = 10) and 5.7-fold (p < 0.01, n = 5), respectively, compared with skin treated with vehicle or sodium lauryl sulfate (used as an irritant control). In vitro translation of poly A+ RNA from all-trans retinoic acid, all-trans retinol, sodium lauryl sulfate, and vehicle-treated human skin demonstrated that the observed increased CRBP mRNA in all-trans retinoic acid- and all-trans retinol-treated skin was able to direct increased (2.3-2.9-fold) CRBP protein synthesis. Riboprobe in situ hybridization revealed that CRBP mRNA was uniformly elevated throughout the epidermis and in dermal cells after all-trans retinoic acid treatment of human skin. Western analysis revealed that CRBP protein was elevated 3.2-fold (p < 0.01, n = 6) and 3.0-fold (p < 0.01, n = 6) after all-trans retinoic acid treatment of human skin in vivo for 24 and 96 h, respectively, compared with vehicle- and sodium lauryl sulfate-treated skin. In addition, functional CRBP levels measured by [3H]all-trans retinol binding were elevated 1.9-fold (p < 0.01, n = 6) and 3.5-fold (p < 0.01, n = 6) at 24 and 94 h, respectively, after all-trans retinoic acid treatment, compared with vehicle- or sodium lauryl sulfate-treated skin. Gel mobility shift analysis revealed that retinoid receptors in nuclear extracts from human skin formed a specific complex with a DNA probe containing the retinoic acid response element in the mouse CRBP gene. Monoclonal antibodies to nuclear retinoid receptors demonstrated that predominantly retinoic acid receptor-alpha/retinoid X receptor-alpha heterodimers bound to the CRBP retinoic acid response element. These data demonstrate that CRBP expression in human skin in vivo is regulated by exogenous all-trans retinoic acid and all-trans retinol.
我们研究了全反式维甲酸和全反式视黄醇对人皮肤中细胞视黄醇结合蛋白(CRBP)mRNA和蛋白表达的体内调节作用。用全反式维甲酸(0.1%)或全反式视黄醇(1.6%)处理人皮肤24小时,与用赋形剂或十二烷基硫酸钠(用作刺激对照)处理的皮肤相比,CRBP mRNA分别诱导增加了5.5倍(p < 0.01,n = 10)和5.7倍(p < 0.01,n = 5)。对来自全反式维甲酸、全反式视黄醇、十二烷基硫酸钠和赋形剂处理的人皮肤的多聚A+RNA进行体外翻译表明,在全反式维甲酸和全反式视黄醇处理的皮肤中观察到的CRBP mRNA增加能够指导CRBP蛋白合成增加(2.3 - 2.9倍)。核糖探针原位杂交显示,用人皮肤进行全反式维甲酸处理后,整个表皮和真皮细胞中的CRBP mRNA均均匀升高。蛋白质免疫印迹分析显示,在体内用人皮肤进行全反式维甲酸处理24小时和96小时后,与用赋形剂和十二烷基硫酸钠处理的皮肤相比,CRBP蛋白分别升高了3.2倍(p < 0.01,n = 6)和3.0倍(p < 0.01,n = 6)。此外,在用全反式维甲酸处理后,分别在24小时和94小时通过[3H]全反式视黄醇结合测定的功能性CRBP水平与用赋形剂或十二烷基硫酸钠处理的皮肤相比,分别升高了1.9倍(p < 0.01,n = 6)和3.5倍(p < 0.01,n = 6)。凝胶迁移率变动分析显示,人皮肤核提取物中的类维生素A受体与含有小鼠CRBP基因中视黄酸反应元件的DNA探针形成了特异性复合物。针对核类维生素A受体的单克隆抗体表明,主要是视黄酸受体α/视黄醇X受体α异二聚体与CRBP视黄酸反应元件结合。这些数据表明,体内人皮肤中的CRBP表达受外源性全反式维甲酸和全反式视黄醇的调节。