CX3CL1/fractalkine is released from apoptotic lymphocytes to stimulate macrophage chemotaxis

被引:353
作者
Truman, Lucy A.
Ford, Catriona A.
Pasikowska, Marta
Pound, John D.
Wilkinson, Sarah J.
Dumitriu, Ingrid E.
Melville, Lynsey
Melrose, Lauren A.
Ogden, Carol Anne
Nibbs, Robert [2 ]
Graham, Gerard [2 ]
Combadiere, Christophe [3 ]
Gregory, Christopher D. [1 ]
机构
[1] Univ Edinburgh, Ctr Inflammat Res, Queens Med Res Inst, MRC, Edinburgh EH16 4TJ, Midlothian, Scotland
[2] Univ Glasgow, Div Immunol Infect & Inflammat, Glasgow, Lanark, Scotland
[3] INSERM, Fac Med Pitie Salpetriere, Lab Immunol Cellulaire, U543, Paris, France
基金
英国医学研究理事会;
关键词
D O I
10.1182/blood-2008-06-162404
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cells undergoing apoptosis are efficiently located and engulfed by phagocytes. The mechanisms by which macrophages, the professional scavenging phagocytes of apoptotic cells, are attracted to sites of apoptosis are poorly defined. Here we show that CX3CL1/fractalkine, a chemokine and intercellular adhesion molecule, is released rapidly from apoptotic lymphocytes, via caspase-and Bcl-2-regulated mechanisms, to attract macrophages. Effective chemotaxis of macrophages to apoptotic lymphocytes is dependent on macrophage fractalkine receptor, CX3CR1. CX3CR1 deficiency caused diminished recruitment of macrophages to germinal centers of lymphoid follicles, sites of high-rate B-cell apoptosis. These results provide the first demonstration of chemokine/chemokine-receptor activity in the navigation of macrophages toward apoptotic cells and identify a mechanism by which macrophage infiltration of tissues containing apoptotic lymphocytes is achieved. (Blood. 2008; 112: 5026-5036)
引用
收藏
页码:5026 / 5036
页数:11
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