Evidence map›Paper›PMID 39042020›Full record

ArticleAmerican journal of respiratory cell and molecular biology2024

Endoplasmic Reticulum Oxidative Stress Promotes Glutathione-Dependent Oxidation of Collagen-1A1 and Promotes Lung Fibroblast Activation.

Joseph E Druso, Maximilian B MacPherson, Shi B Chia, Evan Elko, Reem Aboushousha, David J Seward, Hend Abdelhamid, Cuixia Erickson, Elizabeth Corteselli, Megan Tarte and 9 more

Abstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Enzymatic and non-enzymatic oxidation of fibrillar collagen.Redox report : communications in free radical research · 2026
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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

19 authors.

Joseph E DrusoDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
Maximilian B MacPhersonDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
Shi B ChiaDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
Evan ElkoDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
Reem AboushoushaDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
David J SewardDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
Hend AbdelhamidDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
Cuixia EricksonDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
Elizabeth CorteselliDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
Megan TarteDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
Zhihua PengDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
Daniel BernierDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
Ester ZitoIstituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Matthew D ShouldersDepartment of Chemistry, Massachusetts Institute of Technology, Boston, Massachusetts.
Victor J ThannickalDepartment of Medicine, Tulane University, New Orleans, Louisiana; and.
Steven HuangDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
Albert van der VlietDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
Vikas AnathyDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.
Yvonne M W Janssen-HeiningerDepartments of Pathology and Laboratory Medicine, College of Medicine, University of Vermont, Burlington, Vermont.ORCID 0000-0002-2735-8745

Funding

S-glutathionylation chemistry in fibrotic lung remodelingR35HL135828 · NHLBI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI JANSSEN-HEININGER, YVONNE M. W. · 2017 to 2023
$6.5M
The Role of KCNMB1 and the Large Conductance Potassium (BK) Channel in Myofibroblast Differentiation and Pulmonary FibrosisR01HL127203 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HUANG, STEVEN K · 2015 to 2024
$4.4M
Heterogeneity and Regulation of the DNA Methylome in IPF Mesenchymal CellsR01HL162963 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI STEVEN K HUANG · 2023 to 2026
$2.7M
Collagen Oxidation, Myofibroblast Activation and Age-Associated Pulmonary FibrosisR01AG074488 · NIA · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Yvonne M. W. Janssen-Heininger · 2022 to 2026
$2.4M
Metabolic Reprogramming of the Alveolar Stem Cell Niche in Pulmonary FibrosisR01HL173154 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI Victor J. Thannickal · 2024 to 2026
$1.8M
DUOX1 in fibroblast-macrophage cross-talk in pulmonary fibrosisR21AG075491 · NIA · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI VAN DER VLIET, ALBERT · 2022 to 2023
$429k
Sirtuins in Lung Aging and FibrosisI01BX003056 · VA · SOUTHEAST LOUISIANA VETERANS HEALTH CARE · PI THANNICKAL, VICTOR J. · 2016 to 2025
–
BLRD VA I01 BX003056NHLBI NIH HHS R01AG074488NHLBI NIH HHS R01 HL127203NHLBI NIH HHS R01 HL162963NHLBI NIH HHS R01 HL173154NHLBI NIH HHS R35 HL135828NIA NIH HHS R01 AG074488NIA NIH HHS R21 AG075491Pulmonary Fibrosis Foundation
6 · The paper itself

Abstract

Changes in the oxidative (redox) environment accompany idiopathic pulmonary fibrosis (IPF). S-glutathionylation of reactive protein cysteines is a post-translational event that transduces oxidant signals into biological responses. We recently demonstrated that increases in S-glutathionylation promote pulmonary fibrosis, which was mitigated by the deglutathionylating enzyme glutaredoxin (GLRX). However, the protein targets of S-glutathionylation that promote fibrogenesis remain unknown. In the present study we addressed whether the extracellular matrix is a target for S-glutathionylation. We discovered increases in COL1A1 (collagen 1A1) S-glutathionylation (COL1A1-SSG) in lung tissues from subjects with IPF compared with control subjects in association with increases in ERO1A (endoplasmic reticulum [ER] oxidoreductin 1) and enhanced oxidation of ER-localized PRDX4 (peroxiredoxin 4), reflecting an increased oxidative environment of the ER. Human lung fibroblasts exposed to TGFB1 (transforming growth factor-β1) show increased secretion of COL1A1-SSG. Pharmacologic inhibition of ERO1A diminished the oxidation of PRDX4, attenuated COL1A1-SSG and total COL1A1 concentrations, and dampened fibroblast activation. Absence of

Indexed as

Collagen Type ICollagen Type I, alpha 1 ChainFibroblastsGlutathioneIdiopathic Pulmonary FibrosisLungOxidation-ReductionOxidative StressEndoplasmic ReticulumEndoplasmic Reticulum StressGlutaredoxinsHumansMembrane GlycoproteinsOxidoreductasesPeroxiredoxinsTransforming Growth Factor beta1COL1A1 protein, humanCollagen Type ICollagen Type I, alpha 1 ChainERO1A protein, humanGlutaredoxinsGlutathioneMembrane GlycoproteinsOxidoreductasesPeroxiredoxinsPRDX4 protein, humanTransforming Growth Factor beta1glutaredoxinglutathionylationidiopathic pulmonary fibrosismechanosensingredox

Identifiers

PMID39042020
PMCPMC11568475

What OpenQuestion holds

Textmetadata
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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 OpenQuestion graph.