Synapse Dysfunctions in Multiple Sclerosis

被引:8
|
作者
Schwarz, Karin [1 ]
Schmitz, Frank [1 ]
机构
[1] Saarland Univ, Inst Anat & Cell Biol, Med Sch, Dept Neuroanat, D-66421 Homburg, Germany
关键词
multiple sclerosis; synapse; astrocyte; microglia; glutamate; ionotropic glutamate receptors; synaptopathy; glutamate excitotoxicity; TUMOR-NECROSIS-FACTOR; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; PRO-INFLAMMATORY CYTOKINES; AMPA-RECEPTOR TRAFFICKING; NEURONAL NMDA RECEPTORS; LONG-TERM POTENTIATION; TNF-ALPHA; GLUTAMATE RELEASE; COGNITIVE IMPAIRMENT; RISK-FACTORS;
D O I
10.3390/ijms24021639
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
Multiple sclerosis (MS) is a chronic neuroinflammatory disease of the central nervous system (CNS) affecting nearly three million humans worldwide. In MS, cells of an auto-reactive immune system invade the brain and cause neuroinflammation. Neuroinflammation triggers a complex, multi-faceted harmful process not only in the white matter but also in the grey matter of the brain. In the grey matter, neuroinflammation causes synapse dysfunctions. Synapse dysfunctions in MS occur early and independent from white matter demyelination and are likely correlates of cognitive and mental symptoms in MS. Disturbed synapse/glia interactions and elevated neuroinflammatory signals play a central role. Glutamatergic excitotoxic synapse damage emerges as a major mechanism. We review synapse/glia communication under normal conditions and summarize how this communication becomes malfunctional during neuroinflammation in MS. We discuss mechanisms of how disturbed glia/synapse communication can lead to synapse dysfunctions, signaling dysbalance, and neurodegeneration in MS.
引用
收藏
页数:30
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