Evidence map›Paper›PMID 27381039›Full record

ArticleScientific reports2016

MSC from fetal and adult lungs possess lung-specific properties compared to bone marrow-derived MSC.

Sara Rolandsson Enes, Annika Andersson Sjöland, Ingrid Skog, Lennart Hansson, Hillevi Larsson, Katarina Le Blanc, Leif Eriksson, Leif Bjermer, Stefan Scheding, Gunilla Westergren-Thorsson

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
4.1field-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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
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  14. Host Defense againstJournal of immunology (Baltimore, Md. : 1950) · 2021
    Article
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  16. Article
  17. Article
  18. The vascular nature of lung-resident mesenchymal stem cells.Stem cells translational medicine · 2021
    Article
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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

10 authors at 3 institutions in 1 country.

Sara Rolandsson EnesDepartment of Experimental Medical Science, Lung Biology Unit, Lund University, Lund, Sweden.
Annika Andersson SjölandDepartment of Experimental Medical Science, Lung Biology Unit, Lund University, Lund, Sweden.
Ingrid SkogDepartment of Respiratory Medicine and Allergology, Lund University and Skåne University Hospital, Lund, Sweden.
Lennart HanssonDepartment of Respiratory Medicine and Allergology, Lund University and Skåne University Hospital, Lund, Sweden.
Hillevi LarssonDepartment of Respiratory Medicine and Allergology, Lund University and Skåne University Hospital, Lund, Sweden.
Katarina Le BlancDivision of Clinical Immunology; Centre for Allogeneic Stem Cell Transplantation, Karolinska Institutet, Huddinge University Hospital, Stockholm, Sweden.
Leif ErikssonDepartment of Experimental Medical Science, Lung Biology Unit, Lund University, Lund, Sweden.
Leif BjermerDepartment of Respiratory Medicine and Allergology, Lund University and Skåne University Hospital, Lund, Sweden.
Stefan SchedingLund Stem Cell Center, Lund University, Lund, Sweden.
Gunilla Westergren-ThorssonDepartment of Experimental Medical Science, Lung Biology Unit, Lund University, Lund, Sweden.
Lund University · SESkåne University Hospital · SEKarolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stromal cells (MSC) are multipotent cells with regenerative and immune-modulatory properties. Therefore, MSC have been proposed as a potential cell-therapy for bronchiolitis obliterans syndrome (BOS). On the other hand, there are publications demonstrating that MSC might be involved in the development of BOS. Despite limited knowledge regarding the functional role of tissue-resident lung-MSC, several clinical trials have been performed using MSC, particularly bone marrow (BM)-derived MSC, for various lung diseases. We aimed to compare lung-MSC with the well-characterized BM-MSC. Furthermore, MSC isolated from lung-transplanted patients with BOS were compared to patients without BOS. Our study show that lung-MSCs are smaller, possess a higher colony-forming capacity and have a different cytokine profile compared to BM-MSC. Utilizing gene expression profiling, 89 genes including lung-specific FOXF1 and HOXB5 were found to be significantly different between BM-MSC and lung-MSC. No significant differences in cytokine secretion or gene expression were found between MSC isolated from BOS patients compared recipients without BOS. These data demonstrate that lung-resident MSC possess lung-specific properties. Furthermore, these results show that MSC isolated from lung-transplanted patients with BOS do not have an altered phenotype compared to MSC isolated from good outcome recipients.

Indexed as

AdultBiomarkersBone Marrow CellsBronchiolitis ObliteransCell DifferentiationCell ProliferationCell SeparationCell ShapeColony-Forming Units AssayCytokinesFetusForkhead Transcription FactorsGene Expression RegulationHomeodomain ProteinsHumansLungBiomarkersCytokinesForkhead Transcription FactorsFOXF1 protein, humanHomeodomain ProteinsHOXB5 protein, humanRNA

Identifiers

PMID27381039
PMCPMC4933903
OpenAlexW2462641325

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.