Chertow B S, Moore M R, Blaner W S, Wilford M R, Cordle M B
Department of Medicine, Marshall University School of Medicine, Huntington, WV 25704.
Diabetes. 1989 Dec;38(12):1544-8. doi: 10.2337/diab.38.12.1544.
Vitamin A (retinol) is required for insulin secretion, and retinoic acid substitutes for retinol in this function. To determine if retinol acts at the beta-cell level, we assayed beta-cells of the rat insulinoma (RINm5F) line for cytosolic retinol- and retinoic acid-binding proteins (CRBP and CRABP) by radioimmunoassay (RIA) and [3H]retinol and [3H]retinoic acid binding to cytosol extracts. Furthermore, we tested whether insulin release from cells was affected by addition of retinol or retinoic acid to culture medium. RINm5F cells were grown to near confluence before assay of CRBP and CRABP. Scatchard analysis showed the Kd for retinol to be approximately 6 nM at a level of 4.5 pmol/mg protein or 300,000 sites/cell. Sucrose density-gradient assay showed single discrete peaks migrating at 2S for both retinol and retinoic acid. RIA of whole-cell extracts showed CRBP and CRABP levels of 5.27 +/- 0.41 and 2.95 +/- 0.75 pmol/mg protein, respectively. Retinol (1.75 microM) and retinoic acid (0.175 and 1.75 microM) increased KCl-induced insulin release. Considered together, the presence of CRBP and CRABP in a beta-cell line and the increase in KCl-induced insulin release by retinol and retinoic acid are consistent with the idea that retinol has a functional role in insulin secretion and suggest a potential mechanism of action at the beta-cell level similar to that observed in other retinoid-responsive cells.
维生素A(视黄醇)是胰岛素分泌所必需的,视黄酸在该功能中可替代视黄醇。为了确定视黄醇是否在β细胞水平发挥作用,我们通过放射免疫分析(RIA)以及[3H]视黄醇和[3H]视黄酸与细胞溶质提取物的结合,检测大鼠胰岛素瘤(RINm5F)细胞系的β细胞中的细胞溶质视黄醇结合蛋白和视黄酸结合蛋白(CRBP和CRABP)。此外,我们测试了向培养基中添加视黄醇或视黄酸是否会影响细胞的胰岛素释放。在检测CRBP和CRABP之前,将RINm5F细胞培养至接近汇合状态。Scatchard分析表明,在蛋白质水平为4.5 pmol/mg或300,000个位点/细胞时,视黄醇的解离常数(Kd)约为6 nM。蔗糖密度梯度分析显示,视黄醇和视黄酸在2S处均出现单一离散峰。全细胞提取物的RIA显示,CRBP和CRABP水平分别为5.27±0.41和2.95±0.75 pmol/mg蛋白质。视黄醇(1.75 microM)、视黄酸(0.175和1.75 microM)可增加氯化钾诱导的胰岛素释放。综合来看,β细胞系中存在CRBP和CRABP,以及视黄醇和视黄酸可增加氯化钾诱导的胰岛素释放,这与视黄醇在胰岛素分泌中具有功能作用的观点一致,并提示了在β细胞水平上类似于在其他类维生素A反应性细胞中观察到的潜在作用机制。