Lipopolysaccharide induces the expression of cellular inhibitor of apoptosis protein-2 in human macrophages

被引:42
作者
Cui, XF
Imaizumi, T
Yoshida, H
Tanji, K
Matsumiya, T
Satoh, K
机构
[1] Hirosaki Univ, Sch Med, Dept Vasc Biol, Inst Brain Sci, Hirosaki, Aomori 0368562, Japan
[2] Hirosaki Univ, Sch Med, Inst Brain Sci, Dept Mol Biol, Hirosaki, Aomori 0368562, Japan
[3] Hirosaki Univ, Sch Med, Dept Dent & Oral Surg, Hirosaki, Aomori 0368562, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2000年 / 1524卷 / 2-3期
关键词
cellular inhibitor of apoptosis protein-2; lipopolysaccharide; macrophage; U937; cell; caspase;
D O I
10.1016/S0304-4165(00)00155-0
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
Apoptosis is an important process in normal animal development as well as in diseases, and inhibitor of apoptosis protein (IAP) is one of the important factors that regulate apoptotic cell death. We found that lipopolysaccharide (LPS) enhances the expression of mRNA and protein of cellular IAP-2 (cIAP2) in human monoblastic U937 cells differentiated by phorbol ester pretreatment. cIAP2 mRNA was not detected in undifferentiated U937 cells. mRNAs of cIAP1 and X-chromosome-linked IAP (XIAP) were expressed constitutively and not affected by LPS in both undifferentiated and differentiated cells. LPS stimulated the expression of cIAP2. mRNA and protein in time- and concentration-dependent manners. LPS enhanced the expression of cIAP2 mRNA and protein in human monocyte-derived macrophages, which was associated with the inhibition of the caspase-3 activation, i.e., decrease in active p17 fragment of caspase-3 with simultaneous accumulation of precursor p20 fragment. We conclude that LPS may inhibit apoptosis of macrophages, at least in part, through the induction of cIAP2. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:178 / 182
页数:5
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