Astrocyte contribution to dysfunction, risk and progression in neurodegenerative disorders

被引:225
作者
Brandebura, Ashley N. [1 ]
Paumier, Adrien [1 ]
Onur, Tarik S. [1 ]
Allen, Nicola J. [1 ]
机构
[1] Salk Inst Biol Studies, Mol Neurobiol Lab, La Jolla, CA 92037 USA
关键词
FIBRILLARY ACIDIC PROTEIN; SUBCLINICAL EPILEPTIFORM ACTIVITY; AMYOTROPHIC-LATERAL-SCLEROSIS; ALZHEIMERS-DISEASE; PARKINSONS-DISEASE; REACTIVE ASTROCYTES; APOLIPOPROTEIN-E; MOUSE MODELS; MITOCHONDRIAL DYSFUNCTION; FRONTOTEMPORAL DEMENTIA;
D O I
10.1038/s41583-022-00641-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
There is increasing evidence that neurons are not the only cells affected by and contributing to neurodegenerative disorders. In this Review, Brandebura and colleagues discuss the role astrocytes play in neurodegenerative disorders as initiators of and contributors to disease progression. There is increasing appreciation that non-neuronal cells contribute to the initiation, progression and pathology of diverse neurodegenerative disorders. This Review focuses on the role of astrocytes in disorders including Alzheimer disease, Parkinson disease, Huntington disease and amyotrophic lateral sclerosis. The important roles astrocytes have in supporting neuronal function in the healthy brain are considered, along with studies that have demonstrated how the physiological properties of astrocytes are altered in neurodegenerative disorders and may explain their contribution to neurodegeneration. Further, the question of whether in neurodegenerative disorders with specific genetic mutations these mutations directly impact on astrocyte function, and may suggest a driving role for astrocytes in disease initiation, is discussed. A summary of how astrocyte transcriptomic and proteomic signatures are altered during the progression of neurodegenerative disorders and may relate to functional changes is provided. Given the central role of astrocytes in neurodegenerative disorders, potential strategies to target these cells for future therapeutic avenues are discussed.
引用
收藏
页码:23 / 39
页数:17
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