INTERLEUKIN-4 INHIBITS LIPOPOLYSACCHARIDE-INDUCED EXPRESSION OF PROSTAGLANDIN-H SYNTHASE-2 IN HUMAN ALVEOLAR MACROPHAGES

被引:8
作者
YANO, T
HOPKINS, HA
HEMPEL, SL
MONICK, M
HUNNINGHAKE, GW
机构
[1] UNIV IOWA,COLL MED,DEPT MED,IOWA CITY,IA 52242
[2] UNIV IOWA,COLL MED,VET AFFAIRS MED CTR,IOWA CITY,IA 52242
[3] KAWASAKI HOSP,DEPT INTERNAL MED 2,OKAYAMA,JAPAN
关键词
D O I
10.1002/jcp.1041650110
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Several studies have shown that interleukin-4 (IL-4) down-regulates synthesis of prostaglandin E(2) (PGE(2)). We evaluated the mechanisms for this suppression in human alveolar macrophages (HAMs). Normal HAMs were obtained from healthy nonsmoking volunteers. The cells either remained unstimulated, or were exposed to 10 mu g/ml of lipopolysaccharide (LPS) and/or various amounts of IL-4. LPS alone induced the synthesis of large amounts of PGE(2) and prostaglandin H synthase-2 (PGHS-2) protein. This effect of LPS was suppressed by increasing amounts of IL-4. Expression of LPS-induced PGHS-2 mRNA was also inhibited by IL-4. In addition, IL-4 inhibited expression of CD14, which is a receptor for LPS bound to the LPS-binding protein (LBP). We conclude that IL-4 down-regulates LPS-induced release of PGE(2), by reducing expression of the enzyme, PGHS-2. One potential mechanism for this effect of IL-4 is a reduced expression of CD14, which is the LPS-LBP receptor. (C) 1995 Wiley-Liss, Inc.
引用
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页码:77 / 82
页数:6
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