Evidence map›Paper›PMID 38985878›Full record

ArticleScience advances2024

Pulmonary osteoclast-like cells in silica induced pulmonary fibrosis.

Yoshihiro Hasegawa, Jennifer M Franks, Yusuke Tanaka, Yasuaki Uehara, David F Read, Claire Williams, Sanjay Srivatsan, Lori B Pitstick, Nikolaos M Nikolaidis, Ciara M Shaver and 13 more

Abstract read
In one paragraph

Article in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–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

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Murine models of pulmonary fibrosis: mechanisms, limitations and translational insights.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  5. Multi-omics reveals a novel Cxcr4Clinical and translational medicine · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Mechanobiology and Resolution of Lung Fibrosis.Annual review of physiology · 2026
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Characteristics of Human Donor Lungs Used for Research.American journal of respiratory cell and molecular biology · 2025
    Article
  15. Article
  16. Article
  17. Article
  18. Long noncoding RNA MEG3: an active player in fibrosis.Pharmacological reports : PR · 2025
    Review
  19. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors.

Yoshihiro HasegawaDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA.ORCID 0000-0001-7014-1472
Jennifer M FranksDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID 0000-0003-2400-5431
Yusuke TanakaDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA.
Yasuaki UeharaDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA.ORCID 0000-0002-6439-2715
David F ReadDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Claire WilliamsDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID 0000-0001-5467-149X
Sanjay SrivatsanDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID 0000-0001-7282-0487
Lori B PitstickDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA.ORCID 0009-0006-4775-4661
Nikolaos M NikolaidisDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA.ORCID 0000-0003-1823-4924
Ciara M ShaverDivision of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.ORCID 0000-0002-5677-0288
Jonathan KropskiDivision of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.ORCID 0000-0002-8923-1344
Lorraine B WareDivision of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.ORCID 0000-0002-9429-4702
Chase J TaylorDivision of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.ORCID 0000-0002-7942-0483
Nicholas E BanovichDivision of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.ORCID 0000-0003-2604-3247
Huixing WuDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA.
Jason C GardnerDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA.
Andrew R OsterburgDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA.
Jane J YuDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA.ORCID 0000-0002-0469-9459
Elizabeth J KoprasDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA.ORCID 0000-0001-5429-2609
Steven L TeitelbaumDepartment of Pathology and Immunology, and Division of Bone and Mineral Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Kathryn A Wikenheiser-BrokampDivision of Pathology and Laboratory Medicine and Perinatal Institute, Division of Pulmonary Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.ORCID 0000-0002-2932-3095
Cole TrapnellDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID 0000-0002-8105-4347
Francis X McCormackDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA.ORCID 0000-0001-7168-9464

Funding

REPRODUCTIVE AND DEVELOPMENTAL TOXICOLOGY RESEARCHP30ES006096 · NIEHS · UNIVERSITY OF CINCINNATI · PI PINNEY, SUSAN MENGEL · 1992 to 2022
$35.4M
Spatiotemporal genomic regulation of disease initiation and progression in pulmonary fibrosisR01HL145372 · NHLBI · TRANSLATIONAL GENOMICS RESEARCH INST · PI Nicholas Eli Banovich, Jonathan Andrew Kropski · 2019 to 2026
$6.0M
Pulmonary Macrophage Transplantation for Pulmonary Alveolar ProteinosisR01HL118342 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI TRAPNELL, BRUCE C, TRAPNELL, BRUCE COLSTON · 2014 to 2021
$4.5M
The GOLD Study: Goal of Open Lung Ventilation in DonorsR01HL126176 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WARE, LORRAINE B · 2015 to 2020
$2.8M
Novel Mechanisms of Pulmonary FibrosisR01HL162261 · NHLBI · UNIVERSITY OF CINCINNATI · PI Francis Xavier McCormack · 2023 to 2026
$2.5M
Haptoglobin 2 variant and endothelial glycocalyx shedding in sepsis-induced ARDSR01HL158906 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WARE, LORRAINE B · 2021 to 2024
$2.3M
Pathogenesis-Driven Therapeutic Development for Pulmonary Alveolar MicrolithiasisR01HL127455 · NHLBI · UNIVERSITY OF CINCINNATI · PI MCCORMACK, FRANCIS XAVIER · 2015 to 2018
$1.6M
Mechanisms of airspace inflammation caused by cell-free hemoglobin during ARDSK08HL136888 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SHAVER, CIARA M · 2017 to 2021
$858k
NHLBI NIH HHS K08 HL136888NHLBI NIH HHS R01 HL118342NHLBI NIH HHS R01 HL126176NHLBI NIH HHS R01 HL127455NHLBI NIH HHS R01 HL145372NHLBI NIH HHS R01 HL158906NHLBI NIH HHS R01 HL162261NIEHS NIH HHS P30 ES006096
6 · The paper itself

Abstract

The pathophysiology of silicosis is poorly understood, limiting development of therapies for those who have been exposed to the respirable particle. We explored mechanisms of silica-induced pulmonary fibrosis in human lung samples collected from patients with occupational exposure to silica and in a longitudinal mouse model of silicosis using multiple modalities including whole-lung single-cell RNA sequencing and histological, biochemical, and physiologic assessments. In addition to pulmonary inflammation and fibrosis, intratracheal silica challenge induced osteoclast-like differentiation of alveolar macrophages and recruited monocytes, driven by induction of the osteoclastogenic cytokine, receptor activator of nuclear factor κΒ ligand (RANKL) in pulmonary lymphocytes, and alveolar type II cells. Anti-RANKL monoclonal antibody treatment suppressed silica-induced osteoclast-like differentiation in the lung and attenuated pulmonary fibrosis. We conclude that silica induces differentiation of pulmonary osteoclast-like cells leading to progressive lung injury, likely due to sustained elaboration of bone-resorbing proteases and hydrochloric acid. Interrupting osteoclast-like differentiation may therefore constitute a promising avenue for moderating lung damage in silicosis.

Indexed as

Cell DifferentiationOsteoclastsPulmonary FibrosisSilicon DioxideSilicosisAnimalsDisease Models, AnimalFemaleHumansLungMacrophages, AlveolarMaleMiceRANK LigandRANK LigandSilicon Dioxide

Identifiers

PMID38985878
PMCPMC11235167

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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.