p38 map kinase regulates TNF-α production in human astrocytes and microglia by multiple mechanisms

被引:109
作者
Lee, YB
Schrader, JW
Kim, SU
机构
[1] Univ British Columbia, Dept Med, Div Neurol, Vancouver, BC V6T 2B5, Canada
[2] Univ British Columbia, Biomed Res Ctr, Vancouver, BC, Canada
关键词
cell culture; cytokine; human astrocytes; human microglia; IL-1; beta; lipopolysaccharide; p38 MAP kinase; TNF-alpha;
D O I
10.1006/cyto.2000.0688
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 the vertebrate central nervous system (CNS), tumour necrosis factor-alpha (TNF-alpha) is produced by astrocytes and microglia and mediates cell injury in nerve cells and oligodendrocytes. In the present study, we have used a specific inhibitor of p38 MAP kinase, SB203580 to examine the role of p38 MAP kinase in regulation of TNF-alpha production in human astrocytes and microglia in terms of levels of mRNA and secreted protein. A reverse transcriptase polymerase chain reaction (RT-PCR) analysis showed that increased levels of TNF-alpha mRNA were induced in astrocytes by IL-1 beta treatment, and in microglia by bacterial lipopolysaccharide (LPS), In microglia, treatment with SB203580 reduced the level of TNF-alpha mRNA, but in astrocytes it did not, However, the secretion of TNF-alpha by both astrocytes and microglia was markedly inhibited by SB203580 at a low concentration. TNF-alpha secretion was reduced approximately 80% in astrocytes and 85% in microglia, The results demonstrate a key role played by p38 MAP kinase in upregulation of TNF-alpha mRNA levels in UPS-activated human microglia, whereas p38 MAP kinase is involved in post-transcriptional regulation of TNF-alpha production at translational level in IL-1 beta-activated human astrocytes. (C) 2000 Academic Press.
引用
收藏
页码:874 / 880
页数:7
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