Immune Activation in Brain Aging and Neurodegeneration: Too Much or Too Little?

被引:585
作者
Lucin, Kurt M. [1 ,2 ]
Wyss-Coray, Tony [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
[2] Vet Affairs Palo Alto Hlth Care Syst, Ctr Geriatr Res Educ & Clin, Palo Alto, CA 94304 USA
关键词
AMYOTROPHIC-LATERAL-SCLEROSIS; AMYLOID-BETA-PEPTIDE; TOLL-LIKE RECEPTORS; MARROW-DERIVED MICROGLIA; PROTEIN TRANSGENIC MICE; CENTRAL-NERVOUS-SYSTEM; ALZHEIMERS-DISEASE PATIENTS; GENE-EXPRESSION PROFILE; MOUSE MODEL; PARKINSONS-DISEASE;
D O I
10.1016/j.neuron.2009.08.039
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Until recently, the brain was studied almost exclusively by neuroscientists and the immune system by immunologists, fuelling the notion that these systems represented two isolated entities. However, as more data suggest an important role of the immune system in regulating the progression of brain aging and neurodegenerative disease, it has become clear that the crosstalk between these systems can no longer be ignored and a new interdisciplinary approach is necessary. A central question that emerges is whether immune and inflammatory pathways become hyperactivated with age and promote degeneration or whether insufficient immune responses, which fail to cope with age-related stress, may contribute to disease. We try to explore here the consequences of gain versus loss of function with an emphasis on microglia as sensors and effectors of immune function in the brain, and we discuss the potential role of the peripheral environment in neurodegenerative diseases.
引用
收藏
页码:110 / 122
页数:13
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