4.4 Review

Astrocyte contribution to dysfunction, risk and progression in neurodegenerative disorders

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NATURE REVIEWS NEUROSCIENCE
卷 24, 期 1, 页码 23-39

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NATURE PORTFOLIO
DOI: 10.1038/s41583-022-00641-1

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There is increasing evidence that astrocytes play a significant role in neurodegenerative disorders, both as initiators and contributors to disease progression. This review discusses the involvement of astrocytes in disorders such as Alzheimer's disease, Parkinson's disease, Huntington's disease, and amyotrophic lateral sclerosis, and explores their importance in supporting neuronal function in the healthy brain as well as the changes they undergo in pathological conditions.
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.

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