Diverse and Composite Roles of miRNA in Non-Neuronal Cells and Neuronal Synapses in Alzheimer’s Disease

Xinrong Li, Shih-Chi Chen, Jacque Pak Kan Ip*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

8 Citations (Scopus)
45 Downloads (CityUHK Scholars)

Abstract

Neurons interact with astrocytes, microglia, and vascular cells. These interactions become unbalanced in disease states, resulting in damage to neurons and synapses, and contributing to cognitive impairment. Importantly, synaptic loss and synaptic dysfunction have been considered for years as a main pathological factor of cognitive impairment in Alzheimer’s disease (AD). Recently, miRNAs have emerged as essential regulators of physiological and pathological processes in the brain. Focusing on the role of miRNAs in regulating synaptic functions, as well as different cell types in the brain, offers opportunities for the early prevention, diagnosis, and potential treatment of AD-related cognitive impairment. Here, we review the recent research conducted on miRNAs regulating astrocytes, microglia, cerebrovasculature, and synaptic functions in the context of AD-related cognitive impairment. We also review potential miRNA-related biomarkers and therapeutics, as well as emerging imaging technologies relevant for AD research.
Original languageEnglish
Article number1505
JournalBiomolecules
Volume12
Issue number10
Online published17 Oct 2022
DOIs
Publication statusPublished - Oct 2022

Funding

This work is partially supported by the Lo Kwee-Seong Biomedical Research Fund (J.I.), Faculty Innovation Awards (FIA2020/A/04) from the Faculty of Medicine, CUHK (J.I.), and the Hong Kong Research Grants Council General Research Fund (14117221; J.I.), Area of Excellence Scheme (AoE/M-604/16; J.I.), Theme-based Research Scheme (T13-605/18-W; J.I.).

Research Keywords

  • Alzheimer’s disease
  • astrocyte
  • cerebrovasculature
  • microglia
  • microRNA
  • synapse

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

RGC Funding Information

  • RGC-funded

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