T cell-microglial dialogue in Parkinson's disease and amyotrophic lateral sclerosis: are we listening?

被引:201
作者
Appel, Stanley H. [1 ]
Beers, David R. [1 ]
Henkel, Jenny S. [1 ]
机构
[1] Methodist Hosp, Res Inst, Dept Neurol, Methodist Neurol Inst, Houston, TX 77030 USA
关键词
CENTRAL-NERVOUS-SYSTEM; FACIAL MOTONEURON SURVIVAL; WILD-TYPE MICROGLIA; ALPHA-SYNUCLEIN; MOUSE MODEL; DOPAMINERGIC-NEURONS; NITRIC-OXIDE; MULTIPLE-SCLEROSIS; MOTOR-NEURONS; FAMILIAL ALS;
D O I
10.1016/j.it.2009.09.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Neuroinflammation is a pathological hallmark in Parkinson's disease (PD) and amyotrophic lateral sclerosis (ALS), and is characterized by activated microglia and infiltrating T cells at sites of neuronal injury. In PD and ALS, neurons do not die alone; neuronal injury is non-cell-autonomous and depends on a well-orchestrated dialogue in which neuronally secreted misfolded proteins activate microglia and initiate a self-propagating cycle of neurotoxicity. Diverse populations and phenotypes of CD4(+) T cells crosstalk with microglia, and depending on their activation status, influence this dialogue and promote neuroprotection or neurotoxicity. A greater understanding of the T cell population that mediates these effects, as well as the molecular signals involved should provide targets for neuroprotective immunomodulation to treat these devastating neurodegenerative diseases.
引用
收藏
页码:7 / 17
页数:11
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