Neutrophils sense microbe size and selectively release neutrophil extracellular traps in response to large pathogens

被引:766
|
作者
Branzk, Nora [1 ]
Lubojemska, Aleksandra [1 ]
Hardison, Sarah E. [2 ]
Wang, Qian [1 ]
Gutierrez, Maximiliano G. [3 ]
Brown, Gordon D. [2 ]
Papayannopoulos, Venizelos [1 ]
机构
[1] Natl Inst Med Res, MRC, Div Mol Immunol, London NW7 1AA, England
[2] Univ Aberdeen, Aberdeen Fungal Grp, Inst Med Sci, Aberdeen, Scotland
[3] Natl Inst Med Res, MRC, Div Mycobacterial Res, London NW7 1AA, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
CANDIDA-ALBICANS; MYELOPEROXIDASE DEFICIENCY; PHAGOSOME MATURATION; DECTIN-1; ELASTASE; PHAGOCYTOSIS; MECHANISMS; RECOGNITION; YEAST; ACTIVATION;
D O I
10.1038/ni.2987
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Neutrophils are critical for antifungal defense, but the mechanisms that clear hyphae and other pathogens that are too large to be phagocytosed remain unknown. We found that neutrophils sensed microbe size and selectively released neutrophil extracellular traps (NETs) in response to large pathogens, such as Candida albicans hyphae and extracellular aggregates of Mycobacterium bovis, but not in response to small yeast or single bacteria. NETs were fundamental in countering large pathogens in vivo. Phagocytosis via dectin-1 acted as a sensor of microbe size and prevented NET release by downregulating the translocation of neutrophil elastase (NE) to the nucleus. Dectin-1 deficiency led to aberrant NET release and NET-mediated tissue damage during infection. Size-tailored neutrophil responses cleared large microbes and minimized pathology when microbes were small enough to be phagocytosed.
引用
收藏
页码:1017 / 1025
页数:9
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