Siegenthaler G, Saurat J H, Hotz R, Camenzind M, Merot Y
J Invest Dermatol. 1986 Jan;86(1):42-5. doi: 10.1111/1523-1747.ep12283788.
Cellular retinoid binding proteins are thought to be involved in the molecular action of retinoids, a family of compounds successfully used in the treatment of psoriasis. Therefore, both cellular retinol (CRBP)- and retinoic acid (CRABP)-binding proteins were analyzed in psoriatic skin. Three facts emerged from our study: both CRABP and CRBP are detectable in the skin of psoriatic patients; qualitatively, they both appear similar to the corresponding proteins of normal human skin, in terms of their elution profile and apparent Kd; and quantitatively, only CRABP was found to be 3 times higher in psoriatic plaques as compared to either nonlesional skin of psoriatic patients or the skin of normal subjects. Since psoriatic plaques are particularly responsive to systemic retinoids, specifically to retinoic acid analogues, our results suggest for the first time a link between the levels of CRABP and the responsiveness of a nonneoplastic hyperproliferative tissue to systemic administration of retinoids in the human.
细胞视黄醇结合蛋白被认为参与了类视黄醇的分子作用,类视黄醇是一类成功用于治疗银屑病的化合物。因此,对银屑病皮肤中的细胞视黄醇(CRBP)结合蛋白和视黄酸(CRABP)结合蛋白都进行了分析。我们的研究得出了三个结论:在银屑病患者的皮肤中可检测到CRABP和CRBP;在定性方面,就其洗脱曲线和表观解离常数而言,它们两者看起来都与正常人类皮肤中的相应蛋白相似;在定量方面,与银屑病患者的非皮损皮肤或正常受试者的皮肤相比,仅发现CRABP在银屑病斑块中的含量高3倍。由于银屑病斑块对全身性类视黄醇,特别是对视黄酸类似物特别敏感,我们的结果首次表明在人类中CRABP水平与非肿瘤性增殖性组织对全身性类视黄醇给药的反应性之间存在联系。