Living and dying for inflammation: neutrophils, eosinophils, basophils

被引:192
作者
Geering, Barbara [1 ]
Stoeckle, Christina [1 ]
Conus, Sebastien [1 ]
Simon, Hans-Uwe [1 ]
机构
[1] Univ Bern, Inst Pharmacol, CH-3010 Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
Apoptosis; cytokines; DAMPs; granulocytes; inflammation; PAMPs; THYMIC STROMAL LYMPHOPOIETIN; COLONY-STIMULATING FACTOR; EXTRACELLULAR DNA TRAPS; INNATE LYMPHOID-CELLS; TOLL-LIKE RECEPTORS; IN-VIVO; GRANULOCYTE APOPTOSIS; PROLONGED SURVIVAL; MOLECULAR-MECHANISMS; ENHANCES SURVIVAL;
D O I
10.1016/j.it.2013.04.002
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, eosinophils, and basophils play essential roles during microbe-induced and sterile inflammation. The severity of such inflammatory processes is controlled, at least in part, by factors that regulate cell death and survival of granulocytes. In recent years, major progress has been made in understanding the molecular mechanisms of granulocyte cell death and in identifying novel damage- and pathogen-associated molecular patterns as well as regulatory cytokines impacting granulocyte viability. Furthermore, an increased interest in innate immunity has boosted our overall understanding of granulocyte biology. In this review, we describe and compare factors and mechanisms regulating neutrophil, eosinophil, and basophil lifespan. Because dysregulation of death pathways in granulocytes can contribute to inflammation-associated immunopathology, targeting granulocyte lifespan could be therapeutically promising.
引用
收藏
页码:398 / 409
页数:12
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