Control of autoimmune CNS inflammation by astrocytes

被引:148
|
作者
Rothhammer, Veit [1 ]
Quintana, Francisco J. [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Ann Romney Ctr Neurol Dis, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
Multiple sclerosis; Astrocyte; Cytokine; Chemokine; Blood-brain barrier; CENTRAL-NERVOUS-SYSTEM; NITRIC-OXIDE SYNTHASE; NF-KAPPA-B; MONOCYTE CHEMOATTRACTANT PROTEIN-1; MESSENGER-RNA EXPRESSION; TOLL-LIKE RECEPTOR-3; MULTIPLE-SCLEROSIS; T-CELLS; MURINE ASTROCYTES; INTERFERON-GAMMA;
D O I
10.1007/s00281-015-0515-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Multiple sclerosis is a neurologic disease caused by immune cell infiltration into the central nervous system, resulting in gray and white matter inflammation, progressive demyelination, and neuronal loss. Astrocytes, the most abundant cell population in the central nervous system (CNS), have been considered inert scaffold or housekeeping cells for many years. However, recently, it has become clear that this cell population actively modulates the immune response in the CNS at multiple levels. While being exposed to a plethora of cytokines during ongoing autoimmune inflammation, astrocytes modulate local CNS inflammation by secreting cytokines and chemokines, among other factors. This review article gives an overview of the most recent understanding about cytokine networks operational in astrocytes during autoimmune neuroinflammation and highlights potential targets for immunomodulatory therapies for multiple sclerosis.
引用
收藏
页码:625 / 638
页数:14
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