Hypoxic enhancement of type IV collagen secretion accelerates adipose conversion of 3T3-L1 fibroblasts

被引:15
作者
Tajima, R
Kawaguchi, N
Horino, Y
Takahashi, Y
Toriyama, K
Inou, K
Torii, S
Kitagawa, Y [1 ]
机构
[1] Nagoya Univ, Grad Sch Bioagr Sci, Grad Program Regulat Biol Signals, Chikusa Ku, Nagoya, Aichi 4648601, Japan
[2] Tokyo Univ Pharm & Life Sci, Sch Life Sci, Hachioji, Tokyo 1920392, Japan
[3] Nagoya Univ, Sch Med, Dept Plast & Reconstruct Surg, Nagoya, Aichi 4668560, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2001年 / 1540卷 / 03期
基金
日本学术振兴会;
关键词
adipocyte; collagen; fibroblast; fibrosis hypoxia; prolyl hydroxylation;
D O I
10.1016/S0167-4889(01)00114-8
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
Hypoxic modulation of collagen metabolism appears to be related to pathogenesis of many diseases such as fibrosis of connective tissue after injury and scleroderma. Since most of our understanding of how procollagen assembles within the cell has come from studies on cells cultured under normoxia, it may not be helpful for the etiology of the diseases observed in peripheral tissues under hypoxic conditions. As an experimental model for the hypoxic modulation of collagen metabolism, we cultured 3T3-L1 fibroblasts under low partial oxygen pressure and found that hypoxia enhances secretion of type IV collagen 10-fold and accelerates adipose conversion of the cells. The enhanced secretion of type IV collagen was not accompanied by an appreciable increase of al(IV) and alpha2(IV) mRNAs. Prolyl 4-hydroxylase a increased only 3-fold under hypoxia. We suggest that hypoxia creates an environment of prolyl 4-hydroxylase alpha (2)beta (2) tetramers favorable for the folding of type IV procollagen which has many interruptions of the Gly-Xaa-Yaa repeat. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:179 / 187
页数:9
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