Evidence map›Paper›PMID 40667045›Full record

ArticlebioRxiv : the preprint server for biology2025

A multimodal imaging approach for imaging the metabolic changes resulting from bronchopulmonary dysplasia.

Brittney L Gorman, Zhi Li, Gail Deutsch, Heidi L Huyck, Niana Beishembieva, Heather Olson, Jorge Villazon, Ping Yu, Gloria S Pryhuber, Geremy Clair and 2 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

12 authors.

Brittney L GormanEnvironmental and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, 99354, United States.ORCID 0000-0002-5087-3606
Zhi LiShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, La Jolla, California 92093, United States.
Gail DeutschSeattle Children's Hospital, Seattle, WA 98105, United States.ORCID 0000-0002-0571-0285
Heidi L HuyckDepartment of Pediatrics, University of Rochester Medical Center, Rochester, NY 14642, United States.
Niana BeishembievaEnvironmental and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, 99354, United States.
Heather OlsonEnvironmental and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, 99354, United States.ORCID 0000-0002-4501-9587
Jorge VillazonShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, La Jolla, California 92093, United States.ORCID 0009-0006-8296-5894
Ping YuShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, La Jolla, California 92093, United States.
Gloria S PryhuberDepartment of Pediatrics, University of Rochester Medical Center, Rochester, NY 14642, United States.ORCID 0000-0002-9185-3994
Geremy ClairEnvironmental and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, 99354, United States.ORCID 0000-0003-0478-8520
Lingyan ShiShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, La Jolla, California 92093, United States.ORCID 0000-0003-1373-3206
Christopher R AndertonEnvironmental and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, 99354, United States.ORCID 0000-0002-6170-1033

Funding

BioRepository for INvestigation of Diseases of the Lung (BRINDL) - Phase IIIU01HL148861 · NHLBI · UNIVERSITY OF ROCHESTER · PI GLORIA S PRYHUBER · 2019 to 2026
$9.7M
The Human Lung BioMolecular Multi-Scale Atlas Program (HuBMAP-Lung)U54HL165443 · NHLBI · UNIVERSITY OF ROCHESTER · PI PRYHUBER, GLORIA S · 2022 to 2025
$8.0M
Biorepository for Investigation of Neonatal Diseases of Lung-Normal (BRINDL-NL)U01HL122700 · NHLBI · UNIVERSITY OF ROCHESTER · PI PRYHUBER, GLORIA S · 2014 to 2018
$6.1M
Research Center for Spatiotemporal Lung Imaging and OmicsU01HL148860 · NHLBI · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI ADKINS, JOSHUA N., CARSON, JAMES PAUL · 2019 to 2023
$4.7M
NHLBI NIH HHS U01 HL122700NHLBI NIH HHS U01 HL148860NHLBI NIH HHS U01 HL148861NHLBI NIH HHS U54 HL165443
6 · The paper itself

Abstract

Lung tissue is composed of various functional units, each essential for maintaining the intricate functions of the lung. Disruptions in the molecular and cellular mechanisms in the lung can cause tissue fibrosis, inflammation, and severe breathing difficulties, which are common in conditions such as bronchopulmonary dysplasia (BPD). BPD's molecular changes are not well understood, which hinders effective diagnosis and treatment. Here, we present a new multimodal imaging workflow for detailed molecular and metabolic characterization of tissues at multiple spatial scales. We applied a combined imaging approach using matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) and ultrafast focused light-based imaging & photonics platform (U-FLIP) that included two-photon fluorescence (TPF), second harmonic generation (SHG), and stimulated Raman scattering (SRS). We also developed a hierarchical multimodal registration network (HiMReg) for the precise co-registration of each modality. This approach revealed previously unknown metabolic changes in distinct functional tissue units affected by BPD, including altered lipid distributions, reduced optical redox states, and specific collagen remodeling in bronchioles. Our findings evidenced alterations in lipid composition and metabolism of BPD-affected alveoli compared to healthy tissue, providing novel insights into disease pathophysiology. Our findings elucidate the intricate spatial and molecular complexity of BPD, building on prior research that did not provide the spatial resolution necessary to capture the nuances of metabolic alterations. This multimodal approach offers exceptional insights into disease exploration and could transform the way we study spatially heterogeneous conditions. By providing detailed maps of the metabolic shifts occurring in distinct tissue microanatomical features, the methods developed here could enable the discovery of new therapeutic avenues, making it highly attractive for the field of biomedical research.

Indexed as

LipidomicslungMALDIMass spectrometrySecond harmonic generationStimulated Raman ScatteringTwo photon fluorescence

Identifiers

PMID40667045
PMCPMC12262683

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

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.