Fleet James C, Eksir Faria, Hance Kenneth W, Wood Richard J
Department of Foods and Nutrition, Purdue University, West Lafayette, Indiana 47906, USA.
Am J Physiol Gastrointest Liver Physiol. 2002 Sep;283(3):G618-25. doi: 10.1152/ajpgi.00269.2001.
The parental cell line (P) of Caco-2 cells and two clones, BBe and TC7, were studied at 11 days postconfluence to test the facilitated diffusion model of vitamin D-mediated intestinal calcium absorption (CaTx). Nuclear vitamin D receptor (nVDR) and calbindin D(9k) (CaBP) were measured by Western blot; 1,25-hydroxyvitamin D(3) 24-hydroxylase (CYP24), CaBP, plasma membrane Ca-ATPase (PMCA), and Ca transport channel (CaT1) mRNA levels were examined by RT-PCR; and net apical-to-basolateral CaTx was examined after treating cells with vehicle or 10 nM calcitriol for 8 (mRNA levels) or 48 h (protein, CaBP mRNA, CaTx). nVDR level was lowest in BBe (38% P value) and directly related to CYP24 induction (TC7 = P, which were 1.56 times greater than BBe). nVDR was inversely related to the vitamin D-induced levels of CaT1 mRNA, CaBP mRNA, PMCA mRNA, and net CaTx, with the highest induction seen in BBe. Basal CaBP mRNA (86 times greater than P) and protein levels were highest in TC7 cells and were not associated with higher net CaTx, suggesting CaBP may not be rate limiting for CaTx in these cells.
在汇合后11天对Caco - 2细胞的亲代细胞系(P)以及两个克隆BBe和TC7进行研究,以测试维生素D介导的肠道钙吸收(CaTx)的易化扩散模型。通过蛋白质印迹法检测核维生素D受体(nVDR)和钙结合蛋白D(9k)(CaBP);通过逆转录聚合酶链反应(RT - PCR)检测1,25 - 二羟基维生素D(3)24 - 羟化酶(CYP24)、CaBP、质膜钙ATP酶(PMCA)和钙转运通道(CaT1)的mRNA水平;在用载体或10 nM骨化三醇处理细胞8小时(mRNA水平)或48小时(蛋白质、CaBP mRNA、CaTx)后检测净顶端到基底外侧的CaTx。nVDR水平在BBe中最低(为亲代细胞系P值的38%),且与CYP24的诱导直接相关(TC7 = 亲代细胞系P,比BBe高1.56倍)。nVDR与维生素D诱导后的CaT1 mRNA、CaBP mRNA、PMCA mRNA水平以及净CaTx呈负相关,在BBe中诱导最高。基础CaBP mRNA(比亲代细胞系高86倍)和蛋白质水平在TC7细胞中最高,且与较高的净CaTx无关,这表明CaBP可能不是这些细胞中CaTx的限速因素。