SOCS1 and SOCS3 in the control of CNS immunity

被引:241
作者
Baker, Brandi J. [1 ]
Akhtar, Lisa Nowoslawski [1 ]
Benveniste, Etty N. [1 ]
机构
[1] Univ Alabama Birmingham, Dept Cell Biol, Birmingham, AL 35294 USA
基金
美国国家卫生研究院;
关键词
SPINAL-CORD-INJURY; MULTIPLE-SCLEROSIS PATIENTS; CYTOKINE INTERFERON-GAMMA; BLOOD MONONUCLEAR-CELLS; CD40; GENE-EXPRESSION; GLIOBLASTOMA-MULTIFORME; T-CELLS; AUTOIMMUNE ENCEPHALOMYELITIS; PREVENTS DEVELOPMENT; SENSORY NEURONS;
D O I
10.1016/j.it.2009.07.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the decade following their initial discovery, the suppressor of cytokine signaling (SOCS) proteins have been studied for their potential use as immunomodulators in disease. SOCS proteins, especially SOCS1 and SOCS3, are expressed by immune cells and cells of the central nervous system (CNS) and have the potential to impact immune processes within the CNS, including inflammatory cytokine and chemokine production, activation of microglia, macrophages and astrocytes, immune cell infiltration and autoimmunity. We describe CNS-relevant in vitro and in vivo studies that have examined the function of SOCS1 or SOCS3 under various neuroinflammatory or neuropathological conditions, including exposure of CNS cells to inflammatory cytokines or bacterial infection, demyelinating insults, stroke, spinal cord injury, multiple sclerosis and glioblastoma multiforme.
引用
收藏
页码:392 / 400
页数:9
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