MODULATION OF IL-4 PRODUCTION IN MURINE SPLEEN-CELLS BY PROSTAGLANDINS

被引:17
|
作者
PARKER, CW
HUBER, MG
GODT, SM
机构
[1] Department of Internal Medicine, Division of Immunology, Washington University School of Medicine
关键词
D O I
10.1016/0008-8749(95)80039-L
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recently, it has been reported that IL-4 production by murine Th2 cell lines is insensitive to inhibition by E-type prostaglandins. In the present study, IL-4 production in vitro by freshly isolated concanavalin A (Con A)-stimulated murine spleen cells was readily suppressed by PGE(2) with an I-50 Of 2 nM. Comparable suppression by PGE(2) was seen after priming by anti-CD3 epsilon antibody instead of Con A or with other changes in the culture conditions. PGE(2) was an effective inhibitor after elimination of Ly2.2(+) T cells, consistent with a direct effect on Th2 cells. In the absence of added prostaglandins, IL-4 production was enhanced 1.5- to 7.0-fold by 0.2-2.0 mu M indomethacin, indicating that endogenous arachidonate metabolites such as PGE(2) and PGI(2) regulate IL-4 production in our usual culture system. The inhibition of Th2 cell secretion by PGE(2) in. vitro may have physiologic and pharmacologic implications for the regulation of Th2 cell function and IgE production in vivo. (C) 1995 Academic Press, Inc.
引用
收藏
页码:278 / 285
页数:8
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