Evidence map›Paper›PMID 36719083›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2023

Developmental trajectory of extracellular vesicle characteristics from the lungs of preterm infants.

Meaghan A Ransom, Kaitlyn E Bunn, Nicholas M Negretti, Christopher S Jetter, Zachary J Bressman, Jennifer M S Sucre, Heather H Pua

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% of its field
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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
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  7. Mouse TThe Journal of allergy and clinical immunology · 2025
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  14. The emerging role of extracellular vesicles in bronchopulmonary dysplasia.American journal of physiology. Lung cellular and molecular physiology · 2024
    Review
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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

7 authors at 3 institutions in 1 country.

Meaghan A RansomDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, United States.ORCID 0000-0002-2535-4468
Kaitlyn E BunnDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, United States.
Nicholas M NegrettiDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, United States.
Christopher S JetterDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, United States.
Zachary J BressmanDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, United States.
Jennifer M S SucreDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, United States.ORCID 0000-0002-6613-1439
Heather H PuaDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, United States.ORCID 0000-0002-9271-2608
Nashville Oncology Associates · USVanderbilt University Medical Center · USVanderbilt University · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ben Ho Park · 1995 to 2026
$172.8M
Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MARY Kay WASHINGTON · 2002 to 2026
$29.9M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI OWEN P MCGUINNESS · 2012 to 2026
$29.3M
CLINICAL PHARMACOLOGY TRAINING PROGRAMT32GM007569 · NIGMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Bjorn C Knollmann · 1985 to 2026
$12.4M
TRAINING PROGRAM IN CELLULAR, BIOCHEMICAL, &MOLECULAR ST32GM008554 · NIGMS · VANDERBILT UNIVERSITY · PI PATTON, JAMES G. · 1995 to 2020
$7.4M
Interdisciplinary Training Program in Lung ResearchT32HL094296 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ray Stokes Peebles · 2008 to 2026
$6.3M
Extracellular RNA Communication in Lung InflammationDP2HL152426 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PUA, HEATHER H · 2019 to 2019
$2.5M
Wnt Signaling in Bronchopulmonary DysplasiaK08HL143051 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SUCRE, JENNIFER MALCOLMSRYGLEY · 2019 to 2023
$698k
NCATS NIH HHS UL1 TR002243NCI NIH HHS P30 CA068485NHLBI NIH HHS DP2 HL152426NHLBI NIH HHS K08 HL143051NHLBI NIH HHS L40 HL138848NHLBI NIH HHS T32 HL094296NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P30 DK058404NIGMS NIH HHS T32 GM007569NIGMS NIH HHS T32 GM008554
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are secreted lipid-enclosed particles that have emerged as potential biomarkers and therapeutic agents in lung disease, including bronchopulmonary dysplasia (BPD), a leading complication of preterm birth. Many unanswered questions remain about the content and cargo of EVs in premature infants and their role in lung development. To characterize EVs during human lung development, tracheal aspirates were collected from premature neonates between 22 and 35 wk gestational age and analyzed via nanoparticle tracking analysis, electron microscopy, and bead-based flow cytometry. EVs were detectable across late canalicular through saccular stages of lung development, demonstrating larger sizes earlier in gestation. EVs contained an abundance of the EV-enriched tetraspanins CD9, CD63, and CD81, as well as epithelial cell and immune cell markers. Increases in select surface proteins (CD24 and CD14) on EVs were associated with gestational age and with the risk of BPD. Finally, query of expression data obtained from epithelial cells in a single-cell atlas of murine lung development found that epithelial EV marker expression also changes with developmental time. Together, these data demonstrate an association between EV profile and lung development and provide a foundation for future functional classification of EVs, with the goal of determining their role in cell signaling during development and harnessing their potential as a new therapeutic target in BPD.

Indexed as

Bronchopulmonary DysplasiaExtracellular VesiclesPremature BirthAnimalsFemaleHumansInfant, NewbornInfant, PrematureLungMicebronchopulmonary dysplasiaextracellular vesicleslung development

Identifiers

PMID36719083
PMCPMC10026990
OpenAlexW4318619524

What Socratic holds

Textmetadata
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 Socratic graph.