Microglial Turnover in Ageing-Related Neurodegeneration: Therapeutic Avenue to Intervene in Disease Progression

Microglia are brain-dwelling macrophages and major parts of the neuroimmune system that broadly contribute to brain development, homeostasis, ageing and injury repair in the central nervous system (CNS). Apart from other brain macrophages, they have the ability to constantly sense changes in the bra...

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Main Authors: Shofiul Azam, Md. Ezazul Haque, In-Su Kim, Dong-Kug Choi
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/10/1/150
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author Shofiul Azam
Md. Ezazul Haque
In-Su Kim
Dong-Kug Choi
author_facet Shofiul Azam
Md. Ezazul Haque
In-Su Kim
Dong-Kug Choi
author_sort Shofiul Azam
collection DOAJ
description Microglia are brain-dwelling macrophages and major parts of the neuroimmune system that broadly contribute to brain development, homeostasis, ageing and injury repair in the central nervous system (CNS). Apart from other brain macrophages, they have the ability to constantly sense changes in the brain’s microenvironment, functioning as housekeepers for neuronal well-being and providing neuroprotection in normal physiology. Microglia use a set of genes for these functions that involve proinflammatory cytokines. In response to specific stimuli, they release these proinflammatory cytokines, which can damage and kill neurons via neuroinflammation. However, alterations in microglial functioning are a common pathophysiology in age-related neurodegenerative diseases, such as Alzheimer’s, Parkinson’s, Huntington’s and prion diseases, as well as amyotrophic lateral sclerosis, frontotemporal dementia and chronic traumatic encephalopathy. When their sentinel or housekeeping functions are severely disrupted, they aggravate neuropathological conditions by overstimulating their defensive function and through neuroinflammation. Several pathways are involved in microglial functioning, including the <i>Trem2</i>, <i>Cx3cr1</i> and progranulin pathways, which keep the microglial inflammatory response under control and promote clearance of injurious stimuli. Over time, an imbalance in this system leads to protective microglia becoming detrimental, initiating or exacerbating neurodegeneration. Correcting such imbalances might be a potential mode of therapeutic intervention in neurodegenerative diseases.
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spelling doaj.art-da3f42011e764cf787e39a0b9781f7372023-12-03T13:08:49ZengMDPI AGCells2073-44092021-01-0110115010.3390/cells10010150Microglial Turnover in Ageing-Related Neurodegeneration: Therapeutic Avenue to Intervene in Disease ProgressionShofiul Azam0Md. Ezazul Haque1In-Su Kim2Dong-Kug Choi3Department of Applied Life Science & Integrated Bioscience, Graduate School, BK21 Program, Konkuk University, Chungju 27478, KoreaDepartment of Applied Life Science & Integrated Bioscience, Graduate School, BK21 Program, Konkuk University, Chungju 27478, KoreaDepartment of Integrated Bioscience & Biotechnology, College of Biomedical and Health Science, Research Institute of Inflammatory Disease (RID), Konkuk University, Chungju 27478, KoreaDepartment of Applied Life Science & Integrated Bioscience, Graduate School, BK21 Program, Konkuk University, Chungju 27478, KoreaMicroglia are brain-dwelling macrophages and major parts of the neuroimmune system that broadly contribute to brain development, homeostasis, ageing and injury repair in the central nervous system (CNS). Apart from other brain macrophages, they have the ability to constantly sense changes in the brain’s microenvironment, functioning as housekeepers for neuronal well-being and providing neuroprotection in normal physiology. Microglia use a set of genes for these functions that involve proinflammatory cytokines. In response to specific stimuli, they release these proinflammatory cytokines, which can damage and kill neurons via neuroinflammation. However, alterations in microglial functioning are a common pathophysiology in age-related neurodegenerative diseases, such as Alzheimer’s, Parkinson’s, Huntington’s and prion diseases, as well as amyotrophic lateral sclerosis, frontotemporal dementia and chronic traumatic encephalopathy. When their sentinel or housekeeping functions are severely disrupted, they aggravate neuropathological conditions by overstimulating their defensive function and through neuroinflammation. Several pathways are involved in microglial functioning, including the <i>Trem2</i>, <i>Cx3cr1</i> and progranulin pathways, which keep the microglial inflammatory response under control and promote clearance of injurious stimuli. Over time, an imbalance in this system leads to protective microglia becoming detrimental, initiating or exacerbating neurodegeneration. Correcting such imbalances might be a potential mode of therapeutic intervention in neurodegenerative diseases.https://www.mdpi.com/2073-4409/10/1/150microglianeurodegenerationneuroinflammationmacrophageshomeostasis
spellingShingle Shofiul Azam
Md. Ezazul Haque
In-Su Kim
Dong-Kug Choi
Microglial Turnover in Ageing-Related Neurodegeneration: Therapeutic Avenue to Intervene in Disease Progression
Cells
microglia
neurodegeneration
neuroinflammation
macrophages
homeostasis
title Microglial Turnover in Ageing-Related Neurodegeneration: Therapeutic Avenue to Intervene in Disease Progression
title_full Microglial Turnover in Ageing-Related Neurodegeneration: Therapeutic Avenue to Intervene in Disease Progression
title_fullStr Microglial Turnover in Ageing-Related Neurodegeneration: Therapeutic Avenue to Intervene in Disease Progression
title_full_unstemmed Microglial Turnover in Ageing-Related Neurodegeneration: Therapeutic Avenue to Intervene in Disease Progression
title_short Microglial Turnover in Ageing-Related Neurodegeneration: Therapeutic Avenue to Intervene in Disease Progression
title_sort microglial turnover in ageing related neurodegeneration therapeutic avenue to intervene in disease progression
topic microglia
neurodegeneration
neuroinflammation
macrophages
homeostasis
url https://www.mdpi.com/2073-4409/10/1/150
work_keys_str_mv AT shofiulazam microglialturnoverinageingrelatedneurodegenerationtherapeuticavenuetointerveneindiseaseprogression
AT mdezazulhaque microglialturnoverinageingrelatedneurodegenerationtherapeuticavenuetointerveneindiseaseprogression
AT insukim microglialturnoverinageingrelatedneurodegenerationtherapeuticavenuetointerveneindiseaseprogression
AT dongkugchoi microglialturnoverinageingrelatedneurodegenerationtherapeuticavenuetointerveneindiseaseprogression