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

被引:17
作者
He, Chunxiang [1 ,2 ]
Li, Ze [1 ,2 ]
Yang, Miao [1 ,2 ]
Yu, Wenjing [1 ,2 ]
Luo, Rongsiqing [1 ,2 ]
Zhou, Jinyong [1 ,2 ]
He, Jiawei [1 ,2 ]
Chen, Qi [1 ,2 ]
Song, Zhenyan [1 ,2 ]
Cheng, Shaowu [1 ,2 ]
机构
[1] Hunan Univ Chinese Med, Sch Integrated Chinese & Western Med, Changsha, Hunan, Peoples R China
[2] Hunan Univ Chinese Med, Coll Integrated Tradit Chinese & Western Med, Key Lab Hunan Prov Integrated Tradit Chinese & Wes, Changsha, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; non-coding RNA; neuroinflammation; microglia activation; miRNA; circRNA; lncRNA; SPINAL-CORD-INJURY; ISCHEMIA-REPERFUSION INJURY; DOWN-REGULATION; COGNITIVE IMPAIRMENT; LNCRNA GAS5; INFLAMMATORY RESPONSE; MOUSE MODEL; MEDIATED NEUROINFLAMMATION; REGULATION CONTRIBUTES; CIRCULATING MIR-125B;
D O I
10.2147/JIR.S422114
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 categoriza-tion 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.
引用
收藏
页码:4165 / 4211
页数:47
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