Evidence map›Paper›PMID 38987265›Full record

ArticleNature communications2024

Compartmentalized mitochondrial ferroptosis converges with optineurin-mediated mitophagy to impact airway epithelial cell phenotypes and asthma outcomes.

Kazuhiro Yamada, Claudette St Croix, Donna B Stolz, Yulia Y Tyurina, Vladimir A Tyurin, Laura R Bradley, Alexander A Kapralov, Yanhan Deng, Xiuxia Zhou, Qi Wei and 8 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
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  8. Airway epithelial heterogeneity and mucus plugging in asthmatic bronchioles.American journal of respiratory and critical care medicine · 2026
    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

18 authors.

Kazuhiro YamadaDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA.ORCID 0000-0001-6460-8312
Claudette St CroixDepartment of Cell Biology, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Donna B StolzDepartment of Cell Biology, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Yulia Y TyurinaDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Vladimir A TyurinDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Laura R BradleyDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Alexander A KapralovDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA.ORCID 0000-0002-3006-916X
Yanhan DengDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Xiuxia ZhouDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Qi WeiDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA.ORCID 0009-0002-9616-5055
Bo LiaoDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Nobuhiko FukudaDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Mara SullivanDepartment of Cell Biology, University of Pittsburgh, Pittsburgh, PA, 15261, USA.ORCID 0000-0003-3772-1998
John TrudeauDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Anuradha RayDepartment of Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, PA, 15260, USA.ORCID 0000-0001-6844-8918
Valerian E KaganDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA.ORCID 0000-0002-7245-1885
Jinming ZhaoDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA. JinmingZhao@pitt.edu.ORCID 0000-0003-4700-9734
Sally E WenzelDepartment of Environmental and Occupational Health, School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15261, USA. swenzel@pitt.edu.ORCID 0000-0002-4242-0164

Funding

Project 2 Impact of Innate and Adaptive Immunity At the Airway Epithelium in Severe AsthmaP01AI106684 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Anuradha Ray, Sally E Wenzel · 2015 to 2026
$18.9M
Protein-Oxidized Phospholipid Interactions Determine Epithelial Cell Fate and Asthma Control  R01AI145406 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Sally E Wenzel · 2020 to 2026
$2.9M
Mucin sialylation drives epithelial cell senescence and severe asthmaR01HL153058 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BOUCHER, RICHARD CHARLES, WENZEL, SALLY E · 2020 to 2023
$2.8M
NHLBI NIH HHS R01 HL153058NIAID NIH HHS P01 AI106684NIAID NIH HHS R01 AI145406U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL153058U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI145406U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) P01 AI106684-06A1
6 · The paper itself

Abstract

A stable mitochondrial pool is crucial for healthy cell function and survival. Altered redox biology can adversely affect mitochondria through induction of a variety of cell death and survival pathways, yet the understanding of mitochondria and their dysfunction in primary human cells and in specific disease states, including asthma, is modest. Ferroptosis is traditionally considered an iron dependent, hydroperoxy-phospholipid executed process, which induces cytosolic and mitochondrial damage to drive programmed cell death. However, in this report we identify a lipoxygenase orchestrated, compartmentally-targeted ferroptosis-associated peroxidation process which occurs in a subpopulation of dysfunctional mitochondria, without promoting cell death. Rather, this mitochondrial peroxidation process tightly couples with PTEN-induced kinase (PINK)-1(PINK1)-Parkin-Optineurin mediated mitophagy in an effort to preserve the pool of functional mitochondria and prevent cell death. These combined peroxidation processes lead to altered epithelial cell phenotypes and loss of ciliated cells which associate with worsened asthma severity. Ferroptosis-targeted interventions of this process could preserve healthy mitochondria, reverse cell phenotypic changes and improve disease outcomes.

Indexed as

AsthmaCell Cycle ProteinsEpithelial CellsFerroptosisMembrane Transport ProteinsMitochondriaMitophagyPhenotypeTranscription Factor TFIIIAAnimalsFemaleHumansLipid PeroxidationMaleMiceMiddle AgedCell Cycle ProteinsMembrane Transport ProteinsOPTN protein, humanparkin proteinProtein KinasesPTEN-Induced Putative KinaseTranscription Factor TFIIIAUbiquitin-Protein Ligases

Identifiers

PMID38987265
PMCPMC11237105

What OpenQuestion holds

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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.