c-FLIP Protects Eosinophils from TNF-α-Mediated Cell Death In Vivo

被引:12
作者
Gordy, Claire [1 ]
Liang, Jie [1 ]
Pua, Heather [1 ]
He, You-Wen [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Immunol, Durham, NC 27706 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
NF-KAPPA-B; GLUCOCORTICOID-RECEPTOR; ACTIVATION; APOPTOSIS; INDUCE; NEUTROPHILS; MECHANISMS; EXPRESSION; PATHWAY; DISEASE;
D O I
10.1371/journal.pone.0107724
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Understanding the signals that regulate eosinophil survival and death is critical to developing new treatments for asthma, atopy, and gastrointestinal disease. Previous studies suggest that TNF-alpha stimulation protects eosinophils from apoptosis, and this TNF-alpha-mediated protection is mediated by the upregulation of an unknown protein by NF-kappa B. Here, we show for the first time that eosinophils express the caspase 8-inhibitory protein c-FLIP, and c-FLIP expression is upregulated upon TNF-alpha stimulation. Considering that c-FLIP expression is regulated by NF-kappa B, we hypothesized that c-FLIP might serve as the "molecular switch'' that converts TNFRI activation to a pro-survival signal in eosinophils. Indeed, we found that one c-FLIP isoform, c-FLIPL, is required for mouse eosinophil survival in the presence of TNF-alpha both in vitro and in vivo. Importantly, our results suggest c-FLIP as a potential therapeutic target for the treatment of eosinophil-mediated disease.
引用
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页数:8
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