Targeting granulocyte apoptosis: mechanisms, models, and therapies

被引:104
作者
Duffin, Rodger [1 ]
Leitch, Andrew E. [1 ]
Fox, Sarah [1 ]
Haslett, Chris [1 ]
Rossi, Adriano G. [1 ]
机构
[1] Univ Edinburgh, Queens Med Res Inst, MRC Ctr Inflammat Res, Edinburgh EH16 4TJ, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
inflammation; neutrophil; eosinophil; basophil; apoptosis; phagocytosis; NF-KAPPA-B; INFLAMMATORY CELL APOPTOSIS; COLONY-STIMULATING FACTOR; IN-VIVO; NEUTROPHIL APOPTOSIS; BONE-MARROW; MACROPHAGE PHAGOCYTOSIS; HUMAN BASOPHILS; TNF-ALPHA; PHOSPHATIDYLINOSITOL; 3-KINASE;
D O I
10.1111/j.1600-065X.2010.00922.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The inflammatory process is a complex series of tightly controlled cellular and biochemical events initiated by the immune system, which has evolved to eliminate or contain infectious agents and to repair damaged tissue. Apoptosis is essential for the clearance of potentially injurious inflammatory cells, such as neutrophils, eosinophils, and basophils, and the subsequent efficient resolution of inflammation. In this review, we aim to cover key features of the granulocyte life-cycle ranging from their differentiation within the bone marrow to their maturation and ultimate clearance, with a focus on granulocyte apoptosis and macrophage efferocytosis. We further aim to discuss current and emerging models of inflammation and suggest novel ways of terminating or resolving deleterious inflammatory responses with a specific view to the translation of these strategies into fully realized, pro-resolution therapies.
引用
收藏
页码:28 / 40
页数:13
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