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Author:

Zhang, F. (Zhang, F..) | Ran, Y. (Ran, Y..) | Tahir, M. (Tahir, M..) | Li, Z. (Li, Z..) | Wang, J. (Wang, J..) | Chen, X. (Chen, X..)

Indexed by:

Scopus SCIE

Abstract:

N6-methyladenosine (m6A) is the most abundant post-transcription modification, widely occurring in eukaryotic mRNA and non-coding RNA. m6A modification is highly enriched in the mammalian brain and is associated with neurological diseases like Alzheimer’s disease (AD) and Parkinson’s disease (PD). Ischemic stroke (IS) was discovered to alter the cerebral m6A epi-transcriptome, which might have functional implications in post-stroke pathophysiology. Moreover, it is observed that m6A modification could regulate microglia’s pro-inflammatory and anti-inflammatory responses. Given the critical regulatory role of microglia in the inflammatory processes in the central nervous system (CNS), we speculate that m6A modification could modulate the post-stroke microglial inflammatory responses. This review summarizes the vital regulatory roles of m6A modification in microglia-mediated inflammation and IS. Stroke is associated with a high recurrence rate, understanding the relationship between m6A modification and stroke may help stroke rehabilitation and develop novel therapies in the future. Copyright © 2022 Zhang, Ran, Tahir, Li, Wang and Chen.

Keyword:

ischemic stroke polarization microglia RNA methylation neuroinflammation

Author Community:

  • [ 1 ] [Zhang, F.]Beijing International Science and Technology Cooperation Base for Antiviral Drugs, Faculty of Environment and Life, Beijing University of Technology, Beijing, China
  • [ 2 ] [Ran, Y.]Department of Rehabilitation, Beijing Rehabilitation Hospital, Capital Medical University, Beijing, China
  • [ 3 ] [Tahir, M.]Beijing International Science and Technology Cooperation Base for Antiviral Drugs, Faculty of Environment and Life, Beijing University of Technology, Beijing, China
  • [ 4 ] [Li, Z.]Beijing International Science and Technology Cooperation Base for Antiviral Drugs, Faculty of Environment and Life, Beijing University of Technology, Beijing, China
  • [ 5 ] [Wang, J.]Beijing International Science and Technology Cooperation Base for Antiviral Drugs, Faculty of Environment and Life, Beijing University of Technology, Beijing, China
  • [ 6 ] [Chen, X.]Beijing International Science and Technology Cooperation Base for Antiviral Drugs, Faculty of Environment and Life, Beijing University of Technology, Beijing, China

Reprint Author's Address:

  • [Chen, X.]Beijing International Science and Technology Cooperation Base for Antiviral Drugs, China

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Source :

Frontiers in Cellular Neuroscience

ISSN: 1662-5102

Year: 2022

Volume: 16

5 . 3

JCR@2022

5 . 3 0 0

JCR@2022

ESI Discipline: NEUROSCIENCE & BEHAVIOR;

ESI HC Threshold:37

JCR Journal Grade:1

CAS Journal Grade:2

Cited Count:

WoS CC Cited Count: 63

SCOPUS Cited Count: 33

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 7

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