Evidence map›Paper›PMID 31553626›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2019

Lung inflammatory environments differentially alter mesenchymal stromal cell behavior.

Soraia C Abreu, Sara Rolandsson Enes, Jacob Dearborn, Meagan Goodwin, Amy Coffey, Zachary D Borg, Claúdia C Dos Santos, Matthew J Wargo, Fernanda F Cruz, Roberto Loi and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

33 citing papers in PubMed, 49 citations in OpenAlex.

  1. Trial
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  3. Demographic Factors Affect the BMAC Proteome.Journal of proteome research · 2026
    Article
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  9. Unraveling the Complexities of Mesenchymal Stromal Cell-based Therapies: One Size Doesn't Fit All.American journal of respiratory and critical care medicine · 2024
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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

19 authors at 8 institutions in 5 countries.

Soraia C AbreuDepartment of Medicine, University of Vermont Larner College of Medicine, Burlington, Vermont.
Sara Rolandsson EnesDepartment of Medicine, University of Vermont Larner College of Medicine, Burlington, Vermont.
Jacob DearbornDepartment of Medicine, University of Vermont Larner College of Medicine, Burlington, Vermont.
Meagan GoodwinDepartment of Medicine, University of Vermont Larner College of Medicine, Burlington, Vermont.
Amy CoffeyDepartment of Medicine, University of Vermont Larner College of Medicine, Burlington, Vermont.
Zachary D BorgDepartment of Medicine, University of Vermont Larner College of Medicine, Burlington, Vermont.
Claúdia C Dos SantosDepartments of Medicine and Critical Care Medicine and the Keenan Research Center for Biomedical Science, St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
Matthew J WargoDepartment of Microbial and Molecular Genetics, Larner College of Medicine, University of Vermont, Burlington, Vermont.
Fernanda F CruzLaboratory of Pulmonary Investigation, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Roberto LoiDepartment of Biomedical Sciences, University of Cagliari, Cagliari, Italy.
Michael DeSarnoDepartment of Biostatistics, University of Vermont, Burlington, Vermont.
Takamuru AshikagaDepartment of Biostatistics, University of Vermont, Burlington, Vermont.
Mariana A AntunesLaboratory of Pulmonary Investigation, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Patricia R M RoccoLaboratory of Pulmonary Investigation, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Kathleen D LiuDepartment of Anesthesiology, Medicine and the Cardiovascular Research Institute, University of California, San Francisco, California.
Jae-Woo LeeDepartment of Anesthesiology, Medicine and the Cardiovascular Research Institute, University of California, San Francisco, California.
Michael A MatthayDepartment of Anesthesiology, Medicine and the Cardiovascular Research Institute, University of California, San Francisco, California.
David H McKennaDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota.
Daniel J WeissDepartment of Medicine, University of Vermont Larner College of Medicine, Burlington, Vermont.
University of Vermont · USUniversity of California, San Francisco · USNational Institute of Science and Technology in Regenerative Medicine · BRUniversidade Federal do Rio de Janeiro · BRLund University · SESt. Michael's Hospital · CAUniversity of Cagliari · ITUniversity of Minnesota · US

Funding

Albumin Nanoparticles Incorporating Piceatannol (PANPs) for ALI/ARDS therapyR42HL126456 · NHLBI · NANO BIOTHERAPEUTICS, INC. · PI KANTETI, PRASAD V. S., MALIK, ASRAR B. · 2017 to 2019
$2.7M
Prevention and Early Treatment of Acute Lung InjuryU01HL123004 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MATTHAY, MICHAEL A. · 2014 to 2020
$2.6M
HLS13-13 Albumin nanoparticle based technology to treat ARDSR41HL126456 · NHLBI · CELL BIOLOGICS, INC. · PI BACHMAIER, KURT · 2015 to 2016
$688k
NHLBI NIH HHS HHSN268201000008CNHLBI NIH HHS R41 HL126456NHLBI NIH HHS R42 HL126456NHLBI NIH HHS U01 HL123004
6 · The paper itself

Abstract

Mesenchymal stromal (stem) cells (MSCs) are increasingly demonstrated to ameliorate experimentally induced lung injuries through disease-specific anti-inflammatory actions, thus suggesting that different in vivo inflammatory environments can influence MSC actions. To determine the effects of different representative inflammatory lung conditions, human bone marrow-derived MSCs (hMSCs) were exposed to in vitro culture conditions from bronchoalveolar lavage fluid (BALF) samples obtained from patients with either the acute respiratory distress syndrome (ARDS) or with other lung diseases including acute respiratory exacerbations of cystic fibrosis (CF) (non-ARDS). hMSCs were subsequently assessed for time- and BALF concentration-dependent effects on mRNA expression of selected pro- and anti-inflammatory mediators, and for overall patterns of gene and mRNA expression. Both common and disease-specific patterns were observed in gene expression of different hMSC mediators, notably interleukin (IL)-6. Conditioned media obtained from non-ARDS BALF-exposed hMSCs was more effective in promoting an anti-inflammatory phenotype in monocytes than was conditioned media from ARDS BALF-exposed hMSCs. Neutralizing IL-6 in the conditioned media promoted generation of anti-inflammatory monocyte phenotype. This proof of concept study suggest that different lung inflammatory environments potentially can alter hMSC behaviors. Further identification of these interactions and the driving mechanisms may influence clinical use of MSCs for treating lung diseases.

Indexed as

Anti-Inflammatory AgentsBronchoalveolar Lavage FluidCulture Media, ConditionedCystic FibrosisHumansMesenchymal Stem CellsMesenchymal Stem Cell TransplantationPneumoniaRespiratory Distress SyndromeAnti-Inflammatory AgentsCulture Media, Conditionedacute respiratory distress syndromecystic fibrosisinterleukin 6lung injurymesenchymal stromal (stem) cell

Identifiers

PMID31553626
PMCPMC6962599
OpenAlexW2975592443

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.