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Updated: Oct 8, 2025

Isolation of Cortical Microglia with Preserved Immunophenotype and Functionality From Murine Neonates
Published on: January 30, 2014
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.
Abstract:
The N6-methyladenosine (m6A) modification is the most abundant posttranscriptional mRNA modification in mammalian cells and is dynamically modulated by a series of "writers," "erasers," and "readers." Studies have shown that m6A affects RNA metabolism in terms of RNA processing, nuclear export, translation, and decay. However, the role of the m6A modification in retinal microglial activation remains unclear. Here, we analyzed the single-cell RNA sequencing data of retinal cells from mice with uveitis and found that the m6A-binding protein YTH domain-containing 1 (YTHDC1) was significantly downregulated in retinal microglia in the context of uveitis. Further studies showed that YTHDC1 deficiency resulted in M1 microglial polarization, an increased inflammatory response and the promotion of microglial migration. Mechanistically, YTHDC1 maintained sirtuin 1 (SIRT1) mRNA stability, which reduced signal transducer and activator of transcription 3 (STAT3) phosphorylation, thus inhibiting microglial M1 polarization. Collectively, our data show that YTHDC1 is critical for microglial inflammatory response regulation and can serve as a target for the development of therapeutics for autogenic immune diseases.
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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