Low Expression of YTH Domain-Containing 1 Promotes Microglial M1 Polarization by Reducing the Stability of Sirtuin 1

Hongxiu Zhou1,2,3,4, Zongren Xu1,2,3,4, Xingyun Liao1,2,3,4

  • 1The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

Insights

N6-methyladenosine (m6A) modification impacts RNA metabolism. In uveitis, YTHDC1 downregulation in retinal microglia promotes inflammation and M1 polarization, suggesting YTHDC1 as a therapeutic target for immune diseases.

Area of Science:

  • Immunology
  • Molecular Biology
  • RNA Biology

Background:

  • N6-methyladenosine (m6A) is the most prevalent mRNA modification in mammals.
  • m6A influences RNA processing, export, translation, and decay.
  • The role of m6A in retinal microglial activation is not well understood.

Purpose of the Study:

  • To investigate the role of m6A modification in retinal microglial activation during uveitis.
  • To identify key m6A-binding proteins involved in this process.

Main Methods:

  • Analysis of single-cell RNA sequencing data from mice with uveitis.
  • Investigating the effects of YTHDC1 deficiency in retinal microglia.
  • Assessing microglial polarization, inflammatory response, and migration.

Main Results:

  • YTHDC1 was significantly downregulated in retinal microglia during uveitis.
  • YTHDC1 deficiency led to M1 microglial polarization, increased inflammation, and enhanced migration.
  • YTHDC1 maintains SIRT1 mRNA stability, reducing STAT3 phosphorylation and M1 polarization.

Conclusions:

  • YTHDC1 is crucial for regulating the inflammatory response of retinal microglia.
  • YTHDC1 deficiency exacerbates M1 polarization and inflammation in uveitis.
  • YTHDC1 represents a potential therapeutic target for autoimmune diseases affecting the eye.

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