Neutrophil Apoptosis: A Target for Enhancing the Resolution of Inflammation

被引:60
作者
Filep, Janos G. [1 ]
El Kebir, Driss [1 ]
机构
[1] Univ Montreal, Maisonneuve Rosemont Hosp, Res Ctr, Dept Pathol & Cell Biol, Montreal, PQ H1T 2M4, Canada
基金
加拿大健康研究院;
关键词
NEUTROPHILS; APOPTOSIS; beta(2) INTEGRINS; FPR2/ALX RECEPTOR; ASPIRIN-TRIGGERED LIPOXINS; RESOLUTION OF INFLAMMATION; SERUM-AMYLOID-A; NF-KAPPA-B; CELL-DEATH; MYELOPEROXIDASE; ACTIVATION; EXPRESSION; PROTEIN; PHAGOCYTOSIS; INTEGRINS; PATHWAYS;
D O I
10.1002/jcb.22351
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
Neutrophils are essential for host defense and their programmed cell death and removal are critical for the optimal expression as well as for efficient resolution of inflammation. Delayed neutrophil apoptosis or impaired clearance of apoptotic neutrophils by macrophages contributes to the progression of chronic inflammation. Under most conditions, neutrophils are exposed to multiple factors and their fate would ultimately depend on the balance between pro-survival and pro-apoptotic signals. Life or death decisions are tightly controlled by a complex network of intracellular signaling pathways. Accumulating data indicate that receptors, such as the formyl peptide receptor 2/lipoxin receptor or beta(2)- integrins can generate contrasting cues in neutrophils in a ligand-specific manner and suggest a hierarchy among these signals. In this article, we review recent advances on how pro-apoptosis and pro-survival signals interact to determine the fate of neutrophils and the inflammatory response, and highlight novel pharmacological strategies that could be used to enhance the resolution of inflammation by redirecting neutrophils to apoptosis. J. Cell. Biochem. 108: 1039-1046, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:1039 / 1046
页数:8
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