Evidence map›Paper›PMID 35298658›Full record

ArticleStem cells translational medicine2022

Comparative Effects of Bone Marrow-derived Versus Umbilical Cord Tissue Mesenchymal Stem Cells in an Experimental Model of Bronchopulmonary Dysplasia.

Merline Benny, Benjamin Courchia, Sebastian Shrager, Mayank Sharma, Pingping Chen, Joanne Duara, Krystalenia Valasaki, Michael A Bellio, Andreas Damianos, Jian Huang and 7 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 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 23 citations in OpenAlex.

  1. Development of a peripheral blood transcriptomic gene signature to predict bronchopulmonary dysplasia.American journal of physiology. Lung cellular and molecular physiology · 2023
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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

17 authors at 2 institutions in 1 country.

Merline BennyDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Benjamin CourchiaDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Sebastian ShragerDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Mayank SharmaDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Pingping ChenDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Joanne DuaraDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Krystalenia ValasakiThe Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, FL, USA.
Michael A BellioThe Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, FL, USA.
Andreas DamianosDepartment 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.
Ronald ZambranoDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Augusto SchmidtDepartment 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.
Omaida C VelazquezDepartment of Surgery, University of Miami Miller School of Medicine, Miami, FL, USA.
Joshua M HareThe Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, FL, USA.
Aisha KhanThe Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, FL, USA.
Karen C 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

Bronchopulmonary dysplasia (BPD) is a life-threatening condition in preterm infants with few effective therapies. Mesenchymal stem or stromal cells (MSCs) are a promising therapeutic strategy for BPD. The ideal MSC source for BPD prevention is however unknown. The objective of this study was to compare the regenerative effects of MSC obtained from bone marrow (BM) and umbilical cord tissue (UCT) in an experimental BPD model. In vitro, UCT-MSC demonstrated greater proliferation and expression of anti-inflammatory cytokines as compared to BM-MSC. Lung epithelial cells incubated with UCT-MSC conditioned media (CM) had better-wound healing following scratch injury. UCT-MSC CM and BM-MSC CM had similar pro-angiogenic effects on hyperoxia-exposed pulmonary microvascular endothelial cells. In vivo, newborn rats exposed to normoxia or hyperoxia (85% O2) from postnatal day (P) 1 to 21 were given intra-tracheal (IT) BM or UCT-MSC (1 × 106 cells/50 μL), or placebo (PL) on P3. Hyperoxia PL-treated rats had marked alveolar simplification, reduced lung vascular density, pulmonary vascular remodeling, and lung inflammation. In contrast, administration of both BM-MSC and UCT-MSC significantly improved alveolar structure, lung angiogenesis, pulmonary vascular remodeling, and lung inflammation. UCT-MSC hyperoxia-exposed rats however had greater improvement in some morphometric measures of alveolarization and less lung macrophage infiltration as compared to the BM-MSC-treated group. Together, these findings suggest that BM-MSC and UCT-MSC have significant lung regenerative effects in experimental BPD but UCT-MSC suppresses lung macrophage infiltration and promotes lung epithelial cell healing to a greater degree.

Indexed as

Bronchopulmonary DysplasiaHyperoxiaMesenchymal Stem CellsPneumoniaAnimalsAnimals, NewbornBone MarrowCulture Media, ConditionedDisease Models, AnimalEndothelial CellsHumansInfant, NewbornInfant, PrematureLungRatsRats, Sprague-DawleyCulture Media, Conditionedbone marrowbronchopulmonary dysplasiacell therapymesenchymal stem cellsumbilical cord tissue

Identifiers

PMID35298658
PMCPMC8929420
OpenAlexW4206724061

What OpenQuestion holds

Textmetadata
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.