吡喃结构域
目标2
细胞质
炎症体
先天免疫系统
细胞生物学
转染
基因敲除
生物
分子生物学
核酸
模式识别受体
化学
DNA
受体
基因
生物化学
作者
Tara L. Roberts,Adi Idris,Jasmyn A. Dunn,Gregory M. Kelly,Carol M. Burnton,Samantha Hodgson,Lani Hardy,Valérie Garceau,Matthew J. Sweet,Ian L. Ross,David Hume,Katryn J. Stacey
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2009-01-09
卷期号:323 (5917): 1057-1060
被引量:794
标识
DOI:10.1126/science.1169841
摘要
The mammalian innate immune system is activated by foreign nucleic acids. Detection of double-stranded DNA (dsDNA) in the cytoplasm triggers characteristic antiviral responses and macrophage cell death. Cytoplasmic dsDNA rapidly activated caspase 3 and caspase 1 in bone marrow–derived macrophages. We identified the HIN-200 family member and candidate lupus susceptibility factor, p202, as a dsDNA binding protein that bound stably and rapidly to transfected DNA. Knockdown studies showed p202 to be an inhibitor of DNA-induced caspase activation. Conversely, the related pyrin domain–containing HIN-200 factor, AIM2 (p210), was required for caspase activation by cytoplasmic dsDNA. This work indicates that HIN-200 proteins can act as pattern recognition receptors mediating responses to cytoplasmic dsDNA.
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