Evidence map›Paper›PMID 39402218›Full record

ArticleScientific reports2024

Proteomic analysis of CD29+ Müller cells reveals metabolic reprogramming in rabbit myopia model.

Chae-Eun Moon, Jun-Ki Lee, Hyunjin Kim, Ji-Min Kwon, Yujin Kang, Jinu Han, Yong Woo Ji, Yuri Seo

Abstract read
In one paragraph

Article in Scientific reports, 2024. 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. 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

8 authors.

Chae-Eun Moon *Department of Ophthalmology, Institute of Vision Research, Severance Hospital, Yonsei University College of Medicine, 50 Yonsei‑ro, Seodaemun‑gu, Seoul, 03722, Republic of Korea.
Jun-Ki Lee *Department of Ophthalmology, Institute of Vision Research, Severance Hospital, Yonsei University College of Medicine, 50 Yonsei‑ro, Seodaemun‑gu, Seoul, 03722, Republic of Korea.
Hyunjin KimDepartment of Ophthalmology, Institute of Vision Research, Severance Hospital, Yonsei University College of Medicine, 50 Yonsei‑ro, Seodaemun‑gu, Seoul, 03722, Republic of Korea.
Ji-Min KwonDepartment of Ophthalmology, Institute of Vision Research, Severance Hospital, Yonsei University College of Medicine, 50 Yonsei‑ro, Seodaemun‑gu, Seoul, 03722, Republic of Korea.
Yujin KangDepartment of Ophthalmology, Institute of Vision Research, Severance Hospital, Yonsei University College of Medicine, 50 Yonsei‑ro, Seodaemun‑gu, Seoul, 03722, Republic of Korea.
Jinu HanDepartment of Ophthalmology, Gangnam Severance Hospital, Yonsei University College of Medicine, 211, Eounju-ro, Gangnam-gu, Seoul, 03722, Republic of Korea.
Yong Woo Ji *Department of Ophthalmology, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin-si, 16995, Gyeonggi-do, Republic of Korea. lusita30@yuhs.ac.
Yuri Seo *Department of Ophthalmology, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin-si, 16995, Gyeonggi-do, Republic of Korea. yrseo@yuhs.ac.

Funding

National Research Foundation of Korea 2020R1I1A1A01070668National Research Foundation of Korea 2021R1A2C4001596
6 · The paper itself

Abstract

The prevalence of myopia is rapidly increasing, significantly impacting the quality of life of affected individuals. Prior research by our group revealed reactive gliosis in Müller cells within myopic retina, prompting further investigation of their role in myopia, which remains unclear. In this study, we analyzed protein expression changes in CD29+ Müller cells isolated from a form deprivation-induced rabbit model of myopia using magnetic activated cell sorting to investigate the role of these cells in myopia. As the principal glial cells in the retina, Müller cells exhibited significant alterations in the components of metabolic pathways, particularly glycolysis and angiogenesis, including the upregulation of glycolytic enzymes, such as lactate dehydrogenase A and pyruvate kinase, implicated in the adaptation to increased metabolic demands under myopic stress. Additionally, a decrease in the expression of proteins associated with oxygen transport suggested enhanced vulnerability to oxidative stress. These findings highlight the proactive role of CD29+ Müller cells in modifying the retinal environment in response to myopic stress and provide valuable insights into mechanisms that could help mitigate myopia progression.

Indexed as

Disease Models, AnimalEpendymoglial CellsMyopiaProteomicsAnimalsGlycolysisMetabolic ReprogrammingOxidative StressRabbitsRetinaGlycolysisMüller cellsMyopiaOxidative stressProteomics

Identifiers

PMID39402218
PMCPMC11473955

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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 OpenQuestion graph.