p38丝裂原活化蛋白激酶
先天免疫系统
炭疽杆菌
细胞生物学
激酶
转录因子
MAPK/ERK通路
生物
细胞凋亡
巨噬细胞
丝裂原活化蛋白激酶
蛋白激酶A
免疫系统
微生物学
免疫学
基因
生物化学
细菌
遗传学
体外
作者
Jin Mo Park,Florian R. Greten,Zhiwei Li,Michael Karin
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2002-09-19
卷期号:297 (5589): 2048-2051
被引量:499
标识
DOI:10.1126/science.1073163
摘要
The bacterium Bacillus anthracis causes the death of macrophages, which may allow it to avoid detection by the innate immune system. We found that B. anthracis lethal factor (LF) selectively induces apoptosis of activated macrophages by cleaving the amino-terminal extension of mitogen-activated protein kinase (MAPK) kinases (MKKs) that activate p38 MAPKs. Because macrophages that are deficient in transcription factor nuclear factor κB (NF-κB) are also sensitive to activation-induced death and p38 is required for expression of certain NF-κB target genes, p38 is probably essential for synergistic induction of those NF-κB target genes that prevent apoptosis of activated macrophages. This dismantling of the p38 MAPK module represents a strategy used by B. anthracis to paralyze host innate immunity.
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