首页> 外文期刊>The Journal of investigative dermatology. >All-trans retinoic acid induces cellular retinol-binding protein in human skin in vivo.
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All-trans retinoic acid induces cellular retinol-binding protein in human skin in vivo.

机译:全反式维甲酸在体内诱导人皮肤中的细胞视黄醇结合蛋白。

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摘要

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 acidand all-trans retinol.
机译:我们检查了全反式视黄酸和全反式视黄醇对人体内皮肤视黄醇结合蛋白(CRBP)mRNA和蛋白表达的调节。用全反式视黄酸(0.1%)或全反式视黄醇(1.6%)处理人皮肤24小时,诱导的CRBP mRNA分别为5.5倍(p <0.01,n = 10)和5.7倍(p <0.01,与用赋形剂或十二烷基硫酸钠(用作刺激性对照)治疗的皮肤相比,n = 5)。来自全反式视黄酸,全反式视黄醇,十二烷基硫酸钠和媒介物处理的人皮肤的poly A + RNA的体外翻译表明,在全反式视黄酸和全反式视黄醇处理的皮肤中观察到的CRBP mRNA升高皮肤能够指导增加的CRBP蛋白合成(2.3-2.9倍)。核糖探针原位杂交显示,在人皮肤全反式维甲酸处理后,CRBP mRNA在整个表皮和真皮细胞中均匀升高。 Western分析显示,在体内全反式维甲酸处理24小时和96小时后,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)。分别与媒介物和十二烷基硫酸钠处理过的皮肤相比。此外,通过[3H]全反式视黄醇结合测定的功能性CRBP水平在24小时和94小时分别升高了1.9倍(p <0.01,n = 6)和3.5倍(p <0.01,n = 6)。与经媒介物或十二烷基硫酸钠处理的皮肤相比,经全反式视黄酸处理后的皮肤。凝胶迁移率迁移分析表明,人皮肤核提取物中的类维生素A受体与小鼠CRBP基因中含有视黄酸反应元件的DNA探针形成了特定的复合物。核类视黄醇受体的单克隆抗体证明,主要是视黄酸受体-α/类视黄醇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,人皮肤在体内的CRBP表达受到外源全反式视黄酸和全反式视黄醇的调节。

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