Barsony J, Pike J W, DeLuca H F, Marx S J
Mineral Metabolism Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892.
J Cell Biol. 1990 Dec;111(6 Pt 1):2385-95. doi: 10.1083/jcb.111.6.2385.
Prior studies have given no evidence for regulation of vitamin D receptor (VDR) compartmentalization or subcellular organization. Microwave fixation (9-15 s) and an indirect immunodetection system of avidin-biotin enhancement and phycoerythrin fluorophore resulted in sufficient spatial and temporal resolution to allow analysis of these processes. We studied cultured fibroblasts from normals or from patients with four different types of hereditary defect compromising VDR function (mutant cells). Compartmentalization of VDRs in the absence of 1,25-dihydroxyvitamin D3 (calcitriol) was regulated by serum or estrogen. VDRs were mainly cytoplasmic in cells cultured without serum and phenol red, but VDRs were mainly intranuclear after addition of serum or an estrogen to cells for at least 18 h (slow regulation). Calcitriol initiated a rapid and multistep process (rapid regulation) of reorganization in a portion of VDRs: clumping within 15-45 s, alignment of clumps along fibrils within 30-45 s, perinuclear accumulation of clumps within 45-90 s, and intranuclear accumulation of clumps within 1-3 min. We found similar rapid effects of calcitriol on VDRs in various other types of cultured cells. These sequential VDR pattern changes showed calcitriol dose dependency and calcitriol analogue specificity characteristic for the VDR. In mutant fibroblasts VDR pattern changes after calcitriol were absent or severely disturbed at selected steps. Treatment of normal cells with wheat germ agglutinin, which blocks protein transport through nuclear pores, also blocked calcitriol-dependent translocation of VDRs. We conclude that immunocytology after microwave fixation provides evidence for regulation of VDR organization and localization.
先前的研究没有提供维生素D受体(VDR)区室化或亚细胞组织受调控的证据。微波固定(9 - 15秒)以及抗生物素蛋白-生物素增强和藻红蛋白荧光团的间接免疫检测系统产生了足够的空间和时间分辨率,以允许对这些过程进行分析。我们研究了来自正常人或患有四种不同类型损害VDR功能的遗传性缺陷患者(突变细胞)的培养成纤维细胞。在缺乏1,25 - 二羟基维生素D3(骨化三醇)的情况下,VDR的区室化受血清或雌激素调控。在无血清和酚红的条件下培养的细胞中,VDR主要位于细胞质中,但在向细胞中添加血清或雌激素至少18小时后(缓慢调控),VDR主要位于细胞核内。骨化三醇启动了一部分VDR的快速且多步骤的重组过程(快速调控):在15 - 45秒内聚集,在30 - 45秒内沿纤维排列成块,在45 - 90秒内核周聚集,在1 - 3分钟内核内聚集。我们发现在各种其他类型的培养细胞中,骨化三醇对VDR有类似的快速作用。这些连续的VDR模式变化显示了骨化三醇剂量依赖性以及VDR特有的骨化三醇类似物特异性。在突变的成纤维细胞中,骨化三醇后的VDR模式变化在选定步骤中不存在或受到严重干扰。用小麦胚凝集素处理正常细胞,该凝集素可阻断蛋白质通过核孔的转运,也阻断了骨化三醇依赖性的VDR易位。我们得出结论,微波固定后的免疫细胞化学为VDR的组织和定位受调控提供了证据。