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Non-Coding RNA in Microglia Activation and Neuroinflammation in Alzheimer’s Disease

Alzheimer’s disease (AD) is a neurodegenerative disorder characterized by complex pathophysiological features. Amyloid plaques resulting from extracellular amyloid deposition and neurofibrillary tangles formed by intracellular hyperphosphorylated tau accumulation serve as primary neuropathological c...

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Autores principales: He, Chunxiang, Li, Ze, Yang, Miao, Yu, Wenjing, Luo, Rongsiqing, Zhou, Jinyong, He, Jiawei, Chen, Qi, Song, Zhenyan, Cheng, Shaowu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10519213/
https://www.ncbi.nlm.nih.gov/pubmed/37753266
http://dx.doi.org/10.2147/JIR.S422114
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author He, Chunxiang
Li, Ze
Yang, Miao
Yu, Wenjing
Luo, Rongsiqing
Zhou, Jinyong
He, Jiawei
Chen, Qi
Song, Zhenyan
Cheng, Shaowu
author_facet He, Chunxiang
Li, Ze
Yang, Miao
Yu, Wenjing
Luo, Rongsiqing
Zhou, Jinyong
He, Jiawei
Chen, Qi
Song, Zhenyan
Cheng, Shaowu
author_sort He, Chunxiang
collection PubMed
description Alzheimer’s disease (AD) is a neurodegenerative disorder characterized by complex pathophysiological features. Amyloid plaques resulting from extracellular amyloid deposition and neurofibrillary tangles formed by intracellular hyperphosphorylated tau accumulation serve as primary neuropathological criteria for AD diagnosis. The activation of microglia has been closely associated with these pathological manifestations. Non-coding RNA (ncRNA), a versatile molecule involved in various cellular functions such as genetic information storage and transport, as well as catalysis of biochemical reactions, plays a crucial role in microglial activation. This review aims to investigate the regulatory role of ncRNAs in protein expression by directly targeting genes, proteins, and interactions. Furthermore, it explores the ability of ncRNAs to modulate inflammatory pathways, influence the expression of inflammatory factors, and regulate microglia activation, all of which contribute to neuroinflammation and AD. However, there are still significant controversies surrounding microglial activation and polarization. The categorization into M1 and M2 phenotypes may oversimplify the intricate and multifaceted regulatory processes in microglial response to neuroinflammation. Limited research has been conducted on the role of ncRNAs in regulating microglial activation and inducing distinct polarization states in the context of neuroinflammation. Moreover, the regulatory mechanisms through which ncRNAs govern microglial function continue to be refined. The current understanding of ncRNA regulatory pathways involved in microglial activation remains incomplete and may be influenced by spatial, temporal, and tissue-specific factors. Therefore, further in-depth investigations are warranted. In conclusion, there are ongoing debates and uncertainties regarding the activation and polarization of microglial cells, particularly concerning the categorization into M1 and M2 phenotypes. The study of ncRNA regulation in microglial activation and polarization, as well as its mechanisms, is still in its early stages and requires further investigation. However, this review offers new insights and opportunities for therapeutic approaches in AD. The development of ncRNA-based drugs may hold promise as a new direction in AD treatment.
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spelling pubmed-105192132023-09-26 Non-Coding RNA in Microglia Activation and Neuroinflammation in Alzheimer’s Disease He, Chunxiang Li, Ze Yang, Miao Yu, Wenjing Luo, Rongsiqing Zhou, Jinyong He, Jiawei Chen, Qi Song, Zhenyan Cheng, Shaowu J Inflamm Res Review Alzheimer’s disease (AD) is a neurodegenerative disorder characterized by complex pathophysiological features. Amyloid plaques resulting from extracellular amyloid deposition and neurofibrillary tangles formed by intracellular hyperphosphorylated tau accumulation serve as primary neuropathological criteria for AD diagnosis. The activation of microglia has been closely associated with these pathological manifestations. Non-coding RNA (ncRNA), a versatile molecule involved in various cellular functions such as genetic information storage and transport, as well as catalysis of biochemical reactions, plays a crucial role in microglial activation. This review aims to investigate the regulatory role of ncRNAs in protein expression by directly targeting genes, proteins, and interactions. Furthermore, it explores the ability of ncRNAs to modulate inflammatory pathways, influence the expression of inflammatory factors, and regulate microglia activation, all of which contribute to neuroinflammation and AD. However, there are still significant controversies surrounding microglial activation and polarization. The categorization into M1 and M2 phenotypes may oversimplify the intricate and multifaceted regulatory processes in microglial response to neuroinflammation. Limited research has been conducted on the role of ncRNAs in regulating microglial activation and inducing distinct polarization states in the context of neuroinflammation. Moreover, the regulatory mechanisms through which ncRNAs govern microglial function continue to be refined. The current understanding of ncRNA regulatory pathways involved in microglial activation remains incomplete and may be influenced by spatial, temporal, and tissue-specific factors. Therefore, further in-depth investigations are warranted. In conclusion, there are ongoing debates and uncertainties regarding the activation and polarization of microglial cells, particularly concerning the categorization into M1 and M2 phenotypes. The study of ncRNA regulation in microglial activation and polarization, as well as its mechanisms, is still in its early stages and requires further investigation. However, this review offers new insights and opportunities for therapeutic approaches in AD. The development of ncRNA-based drugs may hold promise as a new direction in AD treatment. Dove 2023-09-21 /pmc/articles/PMC10519213/ /pubmed/37753266 http://dx.doi.org/10.2147/JIR.S422114 Text en © 2023 He et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
He, Chunxiang
Li, Ze
Yang, Miao
Yu, Wenjing
Luo, Rongsiqing
Zhou, Jinyong
He, Jiawei
Chen, Qi
Song, Zhenyan
Cheng, Shaowu
Non-Coding RNA in Microglia Activation and Neuroinflammation in Alzheimer’s Disease
title Non-Coding RNA in Microglia Activation and Neuroinflammation in Alzheimer’s Disease
title_full Non-Coding RNA in Microglia Activation and Neuroinflammation in Alzheimer’s Disease
title_fullStr Non-Coding RNA in Microglia Activation and Neuroinflammation in Alzheimer’s Disease
title_full_unstemmed Non-Coding RNA in Microglia Activation and Neuroinflammation in Alzheimer’s Disease
title_short Non-Coding RNA in Microglia Activation and Neuroinflammation in Alzheimer’s Disease
title_sort non-coding rna in microglia activation and neuroinflammation in alzheimer’s disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10519213/
https://www.ncbi.nlm.nih.gov/pubmed/37753266
http://dx.doi.org/10.2147/JIR.S422114
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