Down-regulation of the macrophage lineage through interaction with OX2 (CD200)

被引:812
作者
Hoek, RM
Ruuls, SR
Murphy, CA
Wright, GJ
Goddard, R
Zurawski, SM
Blom, B
Homola, ME
Streit, WJ
Brown, MH
Barclay, AN
Sedgwick, JD
机构
[1] DNAX Res Inst Mol & Cellular Biol Inc, Palo Alto, CA 94304 USA
[2] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
[3] Univ Florida, Coll Med, Dept Neurosci, Gainesville, FL 32610 USA
[4] Univ Florida, Inst Brain, Gainesville, FL 32610 USA
关键词
D O I
10.1126/science.290.5497.1768
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
OX2 (CD200) is a broadly expressed membrane glycoprotein, shown here to be important for regulation of the macrophage Lineage. In mice lacking CD200, macrophage lineage cells, including brain microglia, exhibited an activated phenotype and were more numerous. Upon facial nerve transection, damaged CD200-deficient neurons elicited an accelerated microglial response. Lack of CD200 resulted in a more rapid onset of experimental autoimmune encephalomyelitis (EAE). Outside the brain, disruption of CD200-CD200 receptor interaction precipitated susceptibility to collagen-induced arthritis(CIA) in mice normally resistant to this disease. Thus, in diverse tissues OX2 delivers an inhibitory signal for the macrophage Lineage.
引用
收藏
页码:1768 / 1771
页数:4
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