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Microglia in Alzheimer’s Disease: A Target for Therapeutic Intervention

Alzheimer’s disease (AD) is one of the most common types of age-related dementia worldwide. In addition to extracellular amyloid plaques and intracellular neurofibrillary tangles, dysregulated microglia also play deleterious roles in the AD pathogenesis. Numerous studies have demonstrated that unbri...

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Autores principales: Zhang, Guimei, Wang, Zicheng, Hu, Huiling, Zhao, Meng, Sun, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651709/
https://www.ncbi.nlm.nih.gov/pubmed/34899188
http://dx.doi.org/10.3389/fncel.2021.749587
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author Zhang, Guimei
Wang, Zicheng
Hu, Huiling
Zhao, Meng
Sun, Li
author_facet Zhang, Guimei
Wang, Zicheng
Hu, Huiling
Zhao, Meng
Sun, Li
author_sort Zhang, Guimei
collection PubMed
description Alzheimer’s disease (AD) is one of the most common types of age-related dementia worldwide. In addition to extracellular amyloid plaques and intracellular neurofibrillary tangles, dysregulated microglia also play deleterious roles in the AD pathogenesis. Numerous studies have demonstrated that unbridled microglial activity induces a chronic neuroinflammatory environment, promotes β-amyloid accumulation and tau pathology, and impairs microglia-associated mitophagy. Thus, targeting microglia may pave the way for new therapeutic interventions. This review provides a thorough overview of the pathophysiological role of the microglia in AD and illustrates the potential avenues for microglia-targeted therapies, including microglial modification, immunoreceptors, and anti-inflammatory drugs.
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spelling pubmed-86517092021-12-09 Microglia in Alzheimer’s Disease: A Target for Therapeutic Intervention Zhang, Guimei Wang, Zicheng Hu, Huiling Zhao, Meng Sun, Li Front Cell Neurosci Cellular Neuroscience Alzheimer’s disease (AD) is one of the most common types of age-related dementia worldwide. In addition to extracellular amyloid plaques and intracellular neurofibrillary tangles, dysregulated microglia also play deleterious roles in the AD pathogenesis. Numerous studies have demonstrated that unbridled microglial activity induces a chronic neuroinflammatory environment, promotes β-amyloid accumulation and tau pathology, and impairs microglia-associated mitophagy. Thus, targeting microglia may pave the way for new therapeutic interventions. This review provides a thorough overview of the pathophysiological role of the microglia in AD and illustrates the potential avenues for microglia-targeted therapies, including microglial modification, immunoreceptors, and anti-inflammatory drugs. Frontiers Media S.A. 2021-11-24 /pmc/articles/PMC8651709/ /pubmed/34899188 http://dx.doi.org/10.3389/fncel.2021.749587 Text en Copyright © 2021 Zhang, Wang, Hu, Zhao and Sun. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular Neuroscience
Zhang, Guimei
Wang, Zicheng
Hu, Huiling
Zhao, Meng
Sun, Li
Microglia in Alzheimer’s Disease: A Target for Therapeutic Intervention
title Microglia in Alzheimer’s Disease: A Target for Therapeutic Intervention
title_full Microglia in Alzheimer’s Disease: A Target for Therapeutic Intervention
title_fullStr Microglia in Alzheimer’s Disease: A Target for Therapeutic Intervention
title_full_unstemmed Microglia in Alzheimer’s Disease: A Target for Therapeutic Intervention
title_short Microglia in Alzheimer’s Disease: A Target for Therapeutic Intervention
title_sort microglia in alzheimer’s disease: a target for therapeutic intervention
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651709/
https://www.ncbi.nlm.nih.gov/pubmed/34899188
http://dx.doi.org/10.3389/fncel.2021.749587
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