Abstract
Astrocytes contribute to brain development and homeostasis and support diverse functions of neurons. These cells also respond to the pathological processes in Alzheimer’s disease (AD). There is still considerable debate concerning the overall contribution of astrocytes to AD pathogenesis since both the protective and harmful effects of these cells on neuronal survival have been documented. This review focuses exclusively on the neurotoxic potential of astrocytes while acknowledging that these cells can contribute to neurodegeneration through other mechanisms, for example, by lowered neurotrophic support. We identify reactive oxygen and nitrogen species, tumor necrosis factor α (TNF-α), glutamate, and matrix metalloproteinase (MMP)-9 as molecules that can be directly toxic to neurons and are released by reactive astrocytes. There is also considerable evidence suggesting their involvement in AD pathogenesis. We further discuss the signaling molecules that trigger the neurotoxic response of astrocytes with a focus on human cells. We also highlight microglia, the immune cells of the brain, as critical regulators of astrocyte neurotoxicity. Nuclear imaging and magnetic resonance spectroscopy (MRS) could be used to confirm the contribution of astrocyte neurotoxicity to AD progression. The molecular mechanisms discussed in this review could be targeted in the development of novel therapies for AD.
Keywords: Reactive astrocytes, neurodegeneration, microglia, reactive oxygen species, reactive nitrogen species, tumor necrosis factor α, glutamate, matrix metalloproteinases.
Current Alzheimer Research
Title:Diversity and Regulation of Astrocyte Neurotoxicity in Alzheimer's Disease
Volume: 18 Issue: 12
Author(s): Sadayuki Hashioka, James G. McLarnon and Andis Klegeris*
Affiliation:
- Department of Biology, University of British Columbia Okanagan Campus, Kelowna, British Columbia, V1V 1V7,Canada
Keywords: Reactive astrocytes, neurodegeneration, microglia, reactive oxygen species, reactive nitrogen species, tumor necrosis factor α, glutamate, matrix metalloproteinases.
Abstract: Astrocytes contribute to brain development and homeostasis and support diverse functions of neurons. These cells also respond to the pathological processes in Alzheimer’s disease (AD). There is still considerable debate concerning the overall contribution of astrocytes to AD pathogenesis since both the protective and harmful effects of these cells on neuronal survival have been documented. This review focuses exclusively on the neurotoxic potential of astrocytes while acknowledging that these cells can contribute to neurodegeneration through other mechanisms, for example, by lowered neurotrophic support. We identify reactive oxygen and nitrogen species, tumor necrosis factor α (TNF-α), glutamate, and matrix metalloproteinase (MMP)-9 as molecules that can be directly toxic to neurons and are released by reactive astrocytes. There is also considerable evidence suggesting their involvement in AD pathogenesis. We further discuss the signaling molecules that trigger the neurotoxic response of astrocytes with a focus on human cells. We also highlight microglia, the immune cells of the brain, as critical regulators of astrocyte neurotoxicity. Nuclear imaging and magnetic resonance spectroscopy (MRS) could be used to confirm the contribution of astrocyte neurotoxicity to AD progression. The molecular mechanisms discussed in this review could be targeted in the development of novel therapies for AD.
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Cite this article as:
Hashioka Sadayuki , McLarnon G. James and Klegeris Andis *, Diversity and Regulation of Astrocyte Neurotoxicity in Alzheimer's Disease, Current Alzheimer Research 2021; 18 (12) . https://dx.doi.org/10.2174/1567205018666211117100342
DOI https://dx.doi.org/10.2174/1567205018666211117100342 |
Print ISSN 1567-2050 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5828 |
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