Plateroti M, Sambuy Y, Nobili F, Bises G, Perozzi G
Istituto Nazionale della Nutrizione, Rome, Italy.
Exp Cell Res. 1993 Sep;208(1):137-47. doi: 10.1006/excr.1993.1231.
This study was undertaken with the aim of investigating the effects of retinoids on the expression of differentiated traits in intestinal cell models. The cell lines used included epithelial cells isolated from fetal rat intestines (FRIC), displaying a relatively undifferentiated phenotype, and the human colon adenocarcinoma cell lines Caco 2 and HT29, which express some of the traits of the mature enterocytes under defined culture conditions. The effects of retinoids were also studied in organ cultures of fetal rat intestine, where the epithelial-mesenchymal interactions are preserved. All-trans-retinol and all-trans-retinoic acid treatments were compared in their ability to regulate the expression of genes coding for proteins involved in retinoid metabolism and for cytoskeletal proteins. The results have shown that the effects of the two retinoids were qualitatively similar. A specific induction of the cellular retinol-binding protein CRBP I mRNA was observed following retinoid treatment in one of the two FRIC lines examined (FRIC B) and in organ culture. The expression of the retinoic acid receptors RAR alpha and gamma was not affected by treatment in any of the cultures examined, while RAR beta was expressed only by the organ cultures and was transcriptionally induced by retinoic acid treatment. The retinoids also induced a reorganization of the actin cytoskeleton in the FRIC B cell line, accompanied by a decrease in the expression of two components of the microvillar cytoskeleton, ezrin and villin. The results obtained in both cell and organ cultures suggest that retinoids alone are not able to trigger the differentiation program in the intestinal epithelial cell, irrespective of the level of differentiation already achieved at the time of treatment.
本研究旨在调查类视黄醇对肠道细胞模型中分化特征表达的影响。所使用的细胞系包括从胎鼠肠道分离的上皮细胞(FRIC),其表现出相对未分化的表型,以及人结肠腺癌细胞系Caco 2和HT29,它们在特定培养条件下表达一些成熟肠上皮细胞的特征。还在保留上皮-间充质相互作用的胎鼠肠道器官培养物中研究了类视黄醇的作用。比较了全反式视黄醇和全反式视黄酸在调节参与类视黄醇代谢的蛋白质和细胞骨架蛋白编码基因表达方面的能力。结果表明,两种类视黄醇的作用在性质上相似。在所检测的两个FRIC细胞系之一(FRIC B)和器官培养物中,类视黄醇处理后观察到细胞视黄醇结合蛋白CRBP I mRNA的特异性诱导。在所检测的任何培养物中,视黄酸受体RARα和γ的表达均不受处理的影响,而RARβ仅在器官培养物中表达,并由视黄酸处理转录诱导。类视黄醇还诱导了FRIC B细胞系中肌动蛋白细胞骨架的重组,同时微绒毛细胞骨架的两个成分埃兹蛋白和绒毛蛋白的表达减少。在细胞和器官培养物中获得的结果表明,无论处理时已达到的分化水平如何,仅类视黄醇都无法触发肠道上皮细胞的分化程序。