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Understanding the neurobiology of CD200 and the CD200 receptor: a therapeutic target for controlling inflammation in human brains?
被引:0
|作者:
Walker, Douglas G.
[1
]
Lue, Lih-Fen
[1
]
机构:
[1] Banner Sun Hlth Res Inst, Lab Neuroinflammat, 10515 West St Fe Dr, Sun City, AZ 85351 USA
关键词:
aging;
alternative activation;
anti-inflammatory signaling;
cell surface protein;
endogenous inflammatory regulator;
inflammation;
neurodegenerative disease;
neuropathology;
D O I:
10.2217/FNL.13.14
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
CD200 and its receptor, CD200 receptor (CD200R), have unique roles in controlling damaging inflammatory processes. At present, the only identified function for CD200 is as a ligand for CD200R. These proteins interact resulting in the activation of anti-inflammatory signaling by CD200R-expressing cells. When this interaction becomes deficient with aging or disease, chronic inflammation occurs. Experimental animal studies have demonstrated the consequences of disrupting CD200-CD200R interactions in the brain, but there have been few studies in human brains. Deficiency in neuronal CD200 may explain the chronic inflammation in human neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease and multiple sclerosis; however, deficits in the microglial expression of CD200R may also be of functional significance. The purpose of this review is to assess the data regarding the role of CD200-CD200R interactions in relation to the brain in order to determine if this could be a therapeutic target for human brain diseases with inflammatory components, and what additional studies are needed.
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页码:321 / 332
页数:12
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