TUMOR-NECROSIS-FACTOR-ALPHA UP-REGULATES HUMAN MICROGLIAL CELL PRODUCTION OF INTERLEUKIN-10 IN-VITRO

被引:97
作者
SHENG, WS
HU, SX
KRAVITZ, FH
PETERSON, PK
CHAO, CC
机构
[1] MINNEAPOLIS MED RES FDN INC,HENNEPIN CTY MED CTR,DEPT MED,NEUROIMMUNOBIOL & HOST DEF LAB,MINNEAPOLIS,MN 55404
[2] UNIV MINNESOTA,SCH MED,MINNEAPOLIS,MN 55404
关键词
D O I
10.1128/CDLI.2.5.604-608.1995
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin (IL)-10 appears to play an important regulatory role in the systemic inflammatory response; however, production of IL-10 within the human central nervous system has not been described, Using cultures of human fetal microglial cells, the resident macrophages of the brain, we investigated the production and regulation of bioactive IL-10. Lipopolysaccharide stimulated acute release of tumor necrosis factor (TNF)-alpha (peak by 8 h) and delayed production of IL-10 (over a 48-h period) in microglial cell cultures, Treatment of microglial cell cultures with TNF-alpha and IL-6 resulted in a dose-dependent release of IL-10. These cytokines also induced expression of IL-10 mRNA. Treatment of microglial cell cultures with IL-10 markedly inhibited TNF-alpha and IL-6 production, These findings suggest that during inflammation within the brain, acute release of TNF-alpha and IL-6 by activated microglia could promote subsequent release of IL-10, which functions to minimize the potential neurotoxic effects of proinflammatory cytokines.
引用
收藏
页码:604 / 608
页数:5
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