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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.
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页码:579 / 584
页数:6
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