Evidence map›Paper›PMID 42436598›Full record

ArticlePhysiological reports2026

A novel two-hit murine model of inhaled occupational exposure-induced lung disease.

Melea Barahona, Ashley DeBie, Logan S Dean, Bethany Klemp, Kaylee Jones, Emmanuel O Oyewole, Mäelis Wahl, Morgan Pauly, Casey McDermott, Francisco J Salguero and 3 more

Abstract read
In one paragraph

Article in Physiological reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Melea BarahonaCell and Molecular Biology Program, Colorado State University, Fort Collins, Colorado, USA.ORCID https://orcid.org/0009-0006-7243-3712
Ashley DeBieDepartment of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, Colorado, USA.
Logan S DeanCell and Molecular Biology Program, Colorado State University, Fort Collins, Colorado, USA.
Bethany KlempDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Kaylee JonesDepartment of Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, Colorado, USA.
Emmanuel O OyewoleDepartment of Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, Colorado, USA.
Mäelis WahlDepartment of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, Colorado, USA.
Morgan PaulyDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Casey McDermottDepartment of Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, Colorado, USA.
Francisco J SalgueroUnited Kingdom Health Security Agency, UKHSA-Porton Down, Salisbury, UK.
G Brooke AndersonDepartment of Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, Colorado, USA.
Marcela Henao-TamayoDepartment of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, USA.
Tara M NordgrenCell and Molecular Biology Program, Colorado State University, Fort Collins, Colorado, USA.ORCID https://orcid.org/0000-0001-6398-8528

Funding

Predoctoral Training in Quantitative Cell & Molecular BiologyT32GM132057 · NIGMS · COLORADO STATE UNIVERSITY · PI Karen Marie Dobos, Brian Munsky · 2019 to 2026
$2.9M
Omega-3 fatty acids induce macrophage IL-22 signaling to promote resolution of dust-induced lung inflammationR01HL158926 · NHLBI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI NORDGREN, TARA M · 2021 to 2025
$2.5M
HHS | National Institutes of Health (NIH) T32GM132057HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL158926NHLBI NIH HHS R01 HL158926NIGMS NIH HHS T32 GM132057
6 · The paper itself

Abstract

The lungs are continuously exposed to environmental insults, rendering the lung epithelium vulnerable to damage and persistent inflammation. Such epithelial damage and prolonged inflammation are hallmark features of various lung diseases, including chronic obstructive pulmonary disease (COPD), pulmonary fibrosis (PF), and lung cancer. Organic dust exposure (ODE), prevalent among workers in livestock and agricultural sectors, is associated with significantly increased risk of these respiratory diseases, yet the underlying mechanisms relating these phenomena remain poorly understood. Here, we have generated a novel murine model of inhaled occupational exposure-induced lung disease using a two-hit approach combining exposure to inhaled organic dust and an established murine model of bleomycin-induced PF to interrogate the signatures of lung damage onset and progression. Following the two-hit treatment in C57Bl/6J mice, we identified a distinct immune cell profile in the bronchoalveolar lavage fluid (BALF), dominated by macrophages and lymphocytes. This response was accompanied by unique inflammatory and injury-related histopathological changes in the lung that have not been observed in models using organic dust or bleomycin alone. These data, combined with additional physiological and cytokine findings, highlight the importance of applying multihit modeling in future work seeking to elucidate the cellular and molecular mechanisms associated with lung disease onset and progression.

Indexed as

Disease Models, AnimalInhalation ExposureLung DiseasesOccupational ExposurePulmonary FibrosisAnimalsBleomycinBronchoalveolar Lavage FluidCytokinesDustLungMaleMiceMice, Inbred C57BLBleomycinCytokinesDustenvironmental toxicantsinflammationorganic dust exposure (ODE)pulmonary fibrosis (PF)

Identifiers

PMID42436598
PMCPMC13356278

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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.