Activation of PKC-β isoforms mediates HNE-induced MCP-1 release by macrophages

被引:46
作者
Nitti, M
Domenicotti, C
d'Abramo, C
Assereto, S
Cottalasso, D
Melloni, E
Poli, G
Biasi, F
Marinari, UM
Pronzato, MA
机构
[1] Univ Genoa, Dept Expt Med, Gen Pathol Sect, I-16132 Genoa, Italy
[2] Univ Genoa, Dept Expt Med, Biochem Sect, Genoa, Italy
[3] Univ Turin, S Luigi Gonzaga Hosp, Dept Clin & Biol Sci, Turin, Italy
关键词
PKC isoenzymes; 4-hydroxynonenal; MCP-1; cell signaling; macrophages;
D O I
10.1016/S0006-291X(02)00512-0
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
4-Hydroxynonenal (FINE) in the concentration range detectable in many pathophysiologic conditions is able to modulate signal transduction cascades and gene expression. Here, we report the stimulating effect of 1 muM HNE on the release of the monocyte chemotactic protem-1 (MCP-1) by murine macrophages. MCP-1-increased export following 1-h cell treatment with HNE proved to be comparable to that exerted by standard amounts of bacterial lipopolysaccharide (LPS). However, the key molecular event in HNE-induced secretion of MCP-1 appeared to be the increased activity of beta-PKC isoforms, which are recognized as playing a role in the regulation of cell protein transport and secretion. On the other hand, in LPS-stimulated cells, the delta isoform was seen to be involved and was probably related to LPS-mediated effects on MCP-1 expression and synthesis. In conclusion, HNE might interact with other pro-inflammatory stimuli, like LPS, in a concerted amplification of MCP-1 production and secretion. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:547 / 552
页数:6
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