Innate immune responses in central nervous system inflammation

被引:44
作者
Finsen, Bente [1 ]
Owens, Trevor [1 ]
机构
[1] Univ So Denmark, Inst Mol Med, DK-5000 Odense C, Denmark
关键词
T cell; Microglia; Astrocyte; Oligodendrocyte; Cytokine; Chemokine; T-CELLS; MULTIPLE-SCLEROSIS; INTERFERON-BETA; DIFFERENTIAL REGULATION; DENDRITIC CELLS; ANGIOTENSIN-II; MYELOID CELLS; BRAIN; MICROGLIA; DEGENERATION;
D O I
10.1016/j.febslet.2011.05.030
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
In autoimmune diseases of the central nervous system (CNS), innate glial cell responses play a key role in determining the outcome of leukocyte infiltration. Access of leukocytes is controlled via complex interactions with glial components of the blood-brain barrier that include angiotensin II receptors on astrocytes and immunoregulatory mediators such as Type I interferons which regulate cellular traffic. Myeloid cells at the blood-brain barrier present antigen to T cells and influence cytokine effector function. Myelin-specific T cells interact with microglia and promote differentiation of oligodendrocyte precursor cells in response to axonal injury. These innate responses offer potential targets for immunomodulatory therapy. (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3806 / 3812
页数:7
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