Evidence map›Paper›PMID 39699914›Full record

ArticleInvestigative ophthalmology & visual science2024

Proteomic Alterations in Retinal Müller Glial Cells Lacking Interleukin-6 Receptor: A Comprehensive Analysis.

Joshua Glass, Rebekah Robinson, Neel Edupuganti, Jeremy Altman, Grace Greenway, Tae Jin Lee, Wenbo Zhi, Ashok Sharma, Shruti Sharma

Abstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 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. Article
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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

9 authors.

Joshua GlassCenter for Biotechnology & Genomic Medicine, Augusta University, Augusta, Georgia, United States.
Rebekah RobinsonCenter for Biotechnology & Genomic Medicine, Augusta University, Augusta, Georgia, United States.
Neel EdupugantiCenter for Biotechnology & Genomic Medicine, Augusta University, Augusta, Georgia, United States.
Jeremy AltmanCenter for Biotechnology & Genomic Medicine, Augusta University, Augusta, Georgia, United States.
Grace GreenwayCenter for Biotechnology & Genomic Medicine, Augusta University, Augusta, Georgia, United States.
Tae Jin LeeCenter for Biotechnology & Genomic Medicine, Augusta University, Augusta, Georgia, United States.
Wenbo ZhiCenter for Biotechnology & Genomic Medicine, Augusta University, Augusta, Georgia, United States.
Ashok SharmaCenter for Biotechnology & Genomic Medicine, Augusta University, Augusta, Georgia, United States.
Shruti SharmaCenter for Biotechnology & Genomic Medicine, Augusta University, Augusta, Georgia, United States.

Funding

Module 3: Gene Expression/ProteomicsP30EY031631 · NEI · AUGUSTA UNIVERSITY · PI Xingjun Fan · 2020 to 2026
$3.6M
Targeting Interleukin-6 cis-trans balance in Müller cell dysfunctionR01EY035995 · NEI · AUGUSTA UNIVERSITY · PI Shruti Sharma · 2024 to 2026
$1.2M
NEI NIH HHS P30 EY031631NEI NIH HHS R01 EY035995
6 · The paper itself

Abstract

Purpose: Interleukin-6 (IL-6) is an inflammatory cytokine implicated in various retinal pathologies and functions primarily through two signaling pathways: cis-signaling via IL-6 binding to its membrane-bound receptor (IL-6Rα), and trans-signaling via IL-6 binding to soluble IL-6 receptor (sIL-6R). Because the differential effects of IL-6 signaling in retinal Müller glial cells (MGCs) remain unclear, we generated an MGC-specific Il6ra-/- knockout (KO) mouse to eliminate IL-6Rα and, consequently, IL-6 cis-signaling in MGCs. In this study, we examined the proteomic changes in MGCs isolated from KO mice lacking a functional IL-6Rα. Methods: The proteomes of MGCs isolated from wild-type (WT) and KO mice were analyzed using liquid chromatography-tandem mass spectrometry (LC-MS/MS) and validated by parallel reaction monitoring (PRM). Relevant biological functions and pathways were examined using Gene Ontology and Ingenuity Pathway Analysis. Results: LC-MS/MS detected 1866 proteins, of which 81 were significantly altered (41 upregulated, 40 downregulated). PRM analysis confirmed differential expression of Ptgis (fold change [FC] = 3.63), Dpep1 (FC = 2.79), Fmo1 (FC = 2.77), Igfbp7 (FC = 2.07), Rpb1 (FC = 1.73), Pygp (FC = 1.46), Niban 1 (FC = 0.58), Mest (FC = 0.48), and Aldh3a1 (FC = 0.30). The significantly altered proteins are involved in oxidative stress balance, inflammation, mitochondrial dysfunction, and regulation of vascular endothelial growth factor (VEGF) signaling. Conclusions: The absence of IL-6Rα in KO MGCs corresponded to significant changes in their proteomic profile, highlighting the impact of autocrine IL-6 signaling on MGC function. This study provides a basis for future research evaluating distinct roles of IL-6 in MGCs and subsequent effects on retinal pathology.

Indexed as

Ependymoglial CellsMice, KnockoutProteomicsReceptors, Interleukin-6Tandem Mass SpectrometryAnimalsChromatography, LiquidInterleukin-6MiceMice, Inbred C57BLProteomeSignal TransductionInterleukin-6ProteomeReceptors, Interleukin-6

Identifiers

PMID39699914
PMCPMC11668349

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.