IL-13 induces serine phosphorylation of cPLA2 in mouse peritoneal macrophages leading to arachidonic acid and PGE2 production and blocks the zymosan-induced serine phosphorylation of cPLA2 and eicosanoid production

被引:10
作者
Rey, A
Quartulli, F
Escoubet, L
Sozzani, P
Caput, D
Ferrara, P
Pipy, B
机构
[1] Hop Rangueil, Lab Macrophages Mediateurs Inflammat & Interact C, Upres EA 2405, F-31403 Toulouse 4, France
[2] Sanofi Rech, F-31676 Labege Innopole, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 1999年 / 1440卷 / 2-3期
关键词
interleukin-13; cytosolic phospholipase A2; mouse peritoneal macrophages; arachidonic acid; serine phosphorylation;
D O I
10.1016/S1388-1981(99)00121-3
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
In a recent investigation, we demonstrated that long-term treatment of macrophages with IL-13 enhances cPLA2 expression and modulates zymosan-stimulated AA mobilization. In the present study, we examine the ability of IL-13 to modify the cPLA2 activity and the AA mobilization of macrophages after a short-period of treatment. We demonstrate that in resting macrophages, IL-13 induces, through a MAP kinase-dependent process, (1) an increase of free AA release within 15 min, followed by increased PGE2 production and (2) a time-dependent serine phosphorylation of cPLA2. Conversely, in macrophages stimulated by zymosan, IL-13 added 30 min before zymosan inhibited the AA release and the serine phosphorylation of cPLA2 induced by the phagocytic agonist. In conclusion, these findings show for the first time that a Th2-type cytokine can upregulate cPLA2 activity and downregulate zymosan-induced AA metabolism. Thus, establishment of the connection between these two events may help to understand the complex regulatory role of IL-13 on the macrophage AA metabolism. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:183 / 193
页数:11
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