Catapult-like release of mitochondrial DNA by eosinophils contributes to antibacterial defense

被引:750
作者
Yousefi, Shida [1 ]
Gold, Jeffrey A. [2 ]
Andina, Nicola [1 ]
Lee, James J. [3 ]
Kelly, Ann M. [2 ]
Kozlowski, Evelyne [1 ]
Schmid, Ines [1 ]
Straumann, Alex [4 ]
Reichenbach, Janine [5 ]
Gleich, Gerald J. [6 ]
Simon, Hans-Uwe [1 ]
机构
[1] Univ Bern, Inst Pharmacol, CH-3010 Bern, Switzerland
[2] Oregon Hlth & Sci Univ, Div Pulm & Crit Care, Portland, OR 97239 USA
[3] Mayo Clin Arizona, Dept Biochem & Mol Biol, Scottsdale, AZ 85259 USA
[4] Kantonsspital Olten, Dept Gastroenterol, CH-4600 Olten, Switzerland
[5] Univ Childrens Hosp, CH-8032 Zurich, Switzerland
[6] Univ Utah, Dept Dermatol, Salt Lake City, UT 84132 USA
基金
瑞士国家科学基金会;
关键词
D O I
10.1038/nm.1855
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
Although eosinophils are considered useful in defense mechanisms against parasites, their exact function in innate immunity remains unclear. The aim of this study is to better understand the role of eosinophils within the gastrointestinal immune system. We show here that lipopolysaccharide from Gram-negative bacteria activates interleukin-5 (IL-5)- or interferon-gamma-primed eosinophils to release mitochondrial DNA in a reactive oxygen species - dependent manner, but independent of eosinophil death. Notably, the process of DNA release occurs rapidly in a catapult-like manner - in less than one second. In the extracellular space, the mitochondrial DNA and the granule proteins form extracellular structures able to bind and kill bacteria both in vitro and under inflammatory conditions in vivo. Moreover, after cecal ligation and puncture, II5-transgenic but not wild-type mice show intestinal eosinophil infiltration and extracellular DNA deposition in association with protection against microbial sepsis. These data suggest a previously undescribed mechanism of eosinophil-mediated innate immune responses that might be crucial for maintaining the intestinal barrier function after inflammation-associated epithelial cell damage, preventing the host from uncontrolled invasion of bacteria.
引用
收藏
页码:949 / 953
页数:5
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