Evidence map›Paper›PMID 35758326›Full record

ArticleStem cells translational medicine2022

Mesenchymal Stem Cell-derived Extracellular Vesicles Prevent Experimental Bronchopulmonary Dysplasia Complicated By Pulmonary Hypertension.

Mayank Sharma, Michael A Bellio, Merline Benny, Shathiyah Kulandavelu, Pingping Chen, Chawisa Janjindamai, Chenxu Han, Liming Chang, Shanique Sterling, Kevin Williams and 12 more

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

27 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
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  3. LncRNA SNHG14 drives alveolar inflammation in bronchopulmonary dysplasia via DNMT3a-mediated epigenetic silencing of miR-214-3p.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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  12. Mesenchymal stem cell therapy for pulmonary hypertension: an update.Frontiers in bioengineering and biotechnology · 2025
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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

22 authors at 2 institutions in 1 country.

Mayank SharmaDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Michael A BellioInterdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, FL, USA.
Merline BennyDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Shathiyah KulandaveluDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.ORCID 0000-0003-0966-7613
Pingping ChenDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Chawisa JanjindamaiDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Chenxu HanBatchelor Children's Research Institute, University of Miami Miller School of Medicine, Miami, FL, USA.
Liming ChangBatchelor Children's Research Institute, University of Miami Miller School of Medicine, Miami, FL, USA.
Shanique SterlingDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Kevin WilliamsDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Andreas DamianosDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Sunil BatlahallyDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Kaitlyn KellyDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Daniela Aguilar-CaballeroDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Ronald ZambranoDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Shaoyi ChenDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Jian HuangDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Shu WuDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Joshua M HareInterdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, FL, USA.ORCID 0000-0002-7751-5032
Augusto SchmidtDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Aisha KhanInterdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, FL, USA.
Karen YoungDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.ORCID 0000-0002-3921-8467
Children’s Institute · USUniversity of Miami · US

Funding

Protective role of CXCR7 in neonatal hyperoxia-induced systemic vascular dysfunction in adulthoodK08HL153945 · NHLBI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BENNY, MERLINE · 2021 to 2025
$747k
NHLBI NIH HHS K08 HL153945
6 · The paper itself

Abstract

Mesenchymal stem cell (MSC) extracellular vesicles (EVs) have beneficial effects in preclinical bronchopulmonary dysplasia and pulmonary hypertension (BPD-PH) models. The optimal source, dosing, route, and duration of effects are however unknown. The objectives of this study were to (a) compare the efficacy of GMP-grade EVs obtained from Wharton's Jelly MSCs (WJ-MSCs) and bone marrow (BM-MSCs), (b) determine the optimal dosing and route of administration, (c) evaluate its long-term effects, and (d) determine how MSC EVs alter the lung transcriptome. Newborn rats exposed to normoxia or hyperoxia (85% O2) from postnatal day (P)1-P14 were given (a) intra-tracheal (IT) BM or WJ-MSC EVs or placebo, (b) varying doses of IT WJ-MSC EVs, or (c) IT or intravenous (IV) WJ-MSC EVs on P3. Rats were evaluated at P14 or 3 months. Early administration of IT BM-MSC or WJ-MSC EVs had similar beneficial effects on lung structure and PH in hyperoxia-exposed rats. WJ-MSC EVs however had superior effects on cardiac remodeling. Low, medium, and high dose WJ-MSC EVs had similar cardiopulmonary regenerative effects. IT and IV WJ-MSC EVs similarly improved vascular density and reduced PH in hyperoxic rats. Gene-set enrichment analysis of transcripts differentially expressed in WJ-MSC EV-treated rats showed that induced transcripts were associated with angiogenesis. Long-term studies demonstrated that a single early MSC EV dose has pulmonary vascular protective effects 3 months after administration. Together, our findings have significant translational implications as it provides critical insight into the optimal source, dosing, route, mechanisms of action, and duration of effects of MSC-EVs for BPD-PH.

Indexed as

Bronchopulmonary DysplasiaExtracellular VesiclesHyperoxiaHypertension, PulmonaryMesenchymal Stem CellsWharton JellyAnimalsDisease Models, AnimalHumansInfant, NewbornRatsbronchopulmonary dysplasiaextracellular vesiclesmesenchymal stem cellpretermpulmonary hypertension

Identifiers

PMID35758326
PMCPMC9397655
OpenAlexW4283589832

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.