Evidence map›Paper›PMID 41601638›Full record

ArticleFrontiers in immunology2025

Revealing the role of regulatory microglial IRF7-NLRP3 interactions in optic nerve damage of normal-tension glaucoma based on single-cell RNA sequencing.

Leyi Qiu, Fengyi Guo, Xinna Liu, Di Zhang, Qi Wang, Mengxian Du, Qianmei Yuan, Shiqi Zhang, Wulian Song, Huiping Yuan

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Neuroinflammation in glaucoma: a myriad of cellular pathways and players.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Leyi QiuDepartment of Ophthalmology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Fengyi GuoDepartment of Ophthalmology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Xinna LiuDepartment of Ophthalmology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Di ZhangDepartment of Ophthalmology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Qi WangDepartment of Ophthalmology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Mengxian DuDepartment of Ophthalmology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Qianmei YuanDepartment of Ophthalmology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Shiqi ZhangDepartment of Ophthalmology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Wulian SongDepartment of Ophthalmology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Huiping YuanDepartment of Ophthalmology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Normal-tension glaucoma (NTG) is a subtype of primary open-angle glaucoma (POAG). Patients with NTG still experience significant optic nerve damage despite maintaining normal intraocular pressures. The mechanism of optic nerve damage in glaucoma with normal pressure is still unclear. Research has shown that OPTN (E50K) mutations exacerbate the inflammatory response of retinal microglia. However, there is still a lack of evidence on how OPTN (E50K) mutations directly regulate their inflammatory pathways through key molecules. This study explores the role of microglial inflammation caused by the interaction between IRF7 and NLRP3 molecules in NTG optic nerve injury. Single-cell RNA sequencing (scRNA-seq) was employed to analyze retinal microglial cells from both wild-type (WT) and OPTN (E50K) mutant mice. The analysis revealed significant enrichment of inflammatory pathways and a critical role of IRF7 in modulating NLRP3 activation. Techniques such as Western blot (WB), qPCR, immunofluorescence (IF), and molecular docking were utilized to confirm the interactions between IRF7 and NLRP3. The findings demonstrate that the OPTN (E50K) mutation reduces the suppressive effect of IRF7 on NLRP3, leading to a pro-inflammatory microglial phenotype and exacerbating the optic nerve damage of NTG. This study provides a new therapeutic target for the treatment of NTG optic nerve damage.

Indexed as

Interferon Regulatory Factor-7Low Tension GlaucomaMicrogliaNLR Family, Pyrin Domain-Containing 3 ProteinOptic NerveAnimalsCell Cycle ProteinsDisease Models, AnimalMaleMembrane Transport ProteinsMiceMice, Inbred C57BLMutationSingle-Cell AnalysisCell Cycle ProteinsInterferon Regulatory Factor-7Irf7 protein, mouseMembrane Transport ProteinsNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseOptn protein, mouseIRF7microgliaNLRP3normal-tension glaucomaoptic nerve damageOPTN (E50K) mutationsingle-cell RNA sequencing

Identifiers

PMID41601638
PMCPMC12832388

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.