Ascorbic acid enhances the expression of type 1 and type 4 collagen and SVCT2 in cultured human skin fibroblasts

被引:72
|
作者
Kishimoto, Yuki [1 ,2 ]
Saito, Norikatsu [3 ]
Kurita, Katsumi [3 ]
Shimokado, Kentaro [2 ]
Maruyama, Naoki [1 ]
Ishigami, Akihito [1 ]
机构
[1] Tokyo Metropolitan Inst Gerontol, Tokyo 1730015, Japan
[2] Tokyo Med & Dent Univ, Dept Geriatr & Vasc Med, Tokyo 1138510, Japan
[3] RISOU Co Ltd, Tokyo 1040061, Japan
关键词
Ascorbic acid; Fibroblast; Sodium-dependent vitamin C transporter; Type; 1; collagen; 4; VITAMIN-C; GENE-EXPRESSION; CELLS; HYDROXYLATION; BIOSYNTHESIS; REDUCTANT; OXIDASE; DAMAGE; MICE;
D O I
10.1016/j.bbrc.2012.11.110
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ascorbic acid (AA) is essential for collagen biosynthesis as a cofactor for prolyl and lysyl hydroxylase and as a stimulus for collagen gene expression. Many studies have evaluated the relationship between AA and collagen expression in short- and long-term effects on cells after a single administration of AA into the culture medium. However, no such study has monitored in detail the stability of AA in medium or the alterations of intracellular AA levels during a protracted interval. Therefore, we examined here intracellular AA levels and stability throughout its exposure to human skin fibroblasts in vitro. Moreover, we determined the effects on type 1 and type 4 collagen and sodium-dependent vitamin C transporter (SVCT) gene expression when medium containing 100 mu M AA was replaced every 24 h for 5 days to avoid depletion of AA. Throughout this long-term culture, intracellular AA levels remained constant; the expression of type 1 and type 4 collagens and SVCT2 mRNA was enhanced, and type 1 procollagen synthesis increased. Thus, these results indicate that human skin fibroblasts exposed to AA over time had rising levels of type 1/type 4 collagens and SVCT2 mRNA expression and type 1 procollagen synthesis. Crown Copyright (C) 2012 Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:579 / 584
页数:6
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