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1,25-二羟基维生素D3对Caco-2细胞增殖和分化的影响。

Effects of 1,25-dihydroxyvitamin D3 on proliferation and differentiation of Caco-2 cells.

作者信息

Halline A G, Davidson N O, Skarosi S F, Sitrin M D, Tietze C, Alpers D H, Brasitus T A

机构信息

Section of Digestive and Liver Diseases, University of Illinois at Chicago 60612.

出版信息

Endocrinology. 1994 Apr;134(4):1710-7. doi: 10.1210/endo.134.4.8137734.

DOI:10.1210/endo.134.4.8137734
PMID:8137734
Abstract

The effect of 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3], or calcitriol, on the proliferation and differentiation of Caco-2 cells was studied. Vitamin D receptor mRNA was detected in both pre- and postconfluent cells, and its abundance was unchanged with time and in response to calcitriol. 1,25-(OH)2D3-binding activity increased during differentiation, but there was no difference in binding between 1,25-(OH)2D3-treated and control cells. 1,25-(OH)2D3 caused a dose-dependent reduction in proliferation, as assessed by [3H]thymidine incorporation and DNA content. 1,25-(OH)2D3 significantly enhanced the normal rise in alkaline phosphatase activity during differentiation and increased alkaline phosphatase mRNA abundance. In contrast, 1,25-(OH)2D3 inhibited the normal rise in sucrase-isomaltase activity and the corresponding mRNA level, although the inhibition occurred after the initial period of cell differentiation (> 10 days postplating). Morphological analysis demonstrated that by day 12 postplating, 1,25-(OH)2D3 increased the mean dome diameter and microvillus length and density. Although 1,25-(OH)2D3 decreases the proliferation of Caco-2 cells and enhances certain parameters of differentiation, not all brush-border hydrolases respond in a similar fashion, making it necessary to interpret with caution their individual use as markers of differentiation.

摘要

研究了1,25 - 二羟基维生素D3[1,25-(OH)2D3],即骨化三醇,对Caco - 2细胞增殖和分化的影响。在汇合前和汇合后的细胞中均检测到维生素D受体mRNA,其丰度不随时间变化,也不受骨化三醇影响。1,25-(OH)2D3结合活性在分化过程中增加,但1,25-(OH)2D3处理组和对照组细胞的结合没有差异。通过[3H]胸腺嘧啶核苷掺入和DNA含量评估,1,25-(OH)2D3导致增殖呈剂量依赖性降低。1,25-(OH)2D3显著增强了分化过程中碱性磷酸酶活性的正常升高,并增加了碱性磷酸酶mRNA丰度。相反,1,25-(OH)2D3抑制了蔗糖酶 - 异麦芽糖酶活性和相应mRNA水平的正常升高,尽管这种抑制发生在细胞分化初期之后(接种后> 10天)。形态学分析表明,接种后第12天,1,25-(OH)2D3增加了平均穹顶直径、微绒毛长度和密度。虽然1,25-(OH)2D3可降低Caco - 2细胞的增殖并增强某些分化参数,但并非所有刷状缘水解酶都有类似反应,因此在将其单独用作分化标志物时必须谨慎解读。

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