INCA, a novel human caspase recruitment domain protein that inhibits interleukin-1β generation

被引:80
作者
Lamkanfi, M [1 ]
Denecker, G [1 ]
Kalai, M [1 ]
D'hondt, K [1 ]
Meeus, A [1 ]
Declercq, W [1 ]
Saelens, X [1 ]
Vandenabeele, P [1 ]
机构
[1] State Univ Ghent VIB, Dept Mol Biomed Res, Unit Mol Signalling & Cell Death, B-9052 Zwijnaarde, Belgium
关键词
D O I
10.1074/jbc.M407891200
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
Using in silico methods for screening the human genome for new caspase recruitment domain (CARD) proteins, we have identified INCA ( Inhibitory CARD) as a protein that shares 81% identity with the prodomain of caspase-1. The INCA gene is located on chromosome 11q22 between the genes of COP/Pseudo-ICE and ICEBERG, two other CARD proteins that arose from caspase-1 gene duplications. We show that INCA mRNA is expressed in many tissues. INCA is specifically upregulated by interferon-gamma in the monocytic cell lines THP-1 and U937. INCA physically interacts with procaspase-1 and blocks the release of mature IL-1beta from LPS-stimulated macrophages. Unlike COP/Pseudo-ICE and procaspase-1, INCA does not interact with RIP2 and does not induce NF-kappaB activation. Our data show that INCA is a novel intracellular regulator of procaspase-1 activation, involved in the regulation of pro-IL-1beta processing and its release during inflammation.
引用
收藏
页码:51729 / 51738
页数:10
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