Evidence map›Paper›PMID 25889287›Full record

ArticleStem cell research & therapy2015

Adipose-derived mesenchymal stromal cells modulate tendon fibroblast responses to macrophage-induced inflammation in vitro.

Cionne N Manning, Catherine Martel, Shelly E Sakiyama-Elbert, Matthew J Silva, Shivam Shah, Richard H Gelberman, Stavros Thomopoulos

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 2 pooled it
9.6field-weighted citation impact, top 1% 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

70 citing papers in PubMed, 2 syntheses or guidelines pooled it, 137 citations in OpenAlex.

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  20. Equine peripheral blood CD14Veterinary immunology and immunopathology · 2023
    Article

10 more citing papers are in PubMed but not listed here.

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 1 institution in 2 countries.

Cionne N ManningDepartment of Orthopedic Surgery, Washington University, 425 S Euclid, Box 8233, St Louis, MO, 63110, USA. cionnemanning@gmail.com.
Catherine MartelDepartment of Pathology and Immunology, Washington University, 425 S Euclid, Box 8233, St Louis, MO, 63110, USA. catmartel@gmail.com.
Shelly E Sakiyama-ElbertDepartment of Biomedical Engineering, Washington University, One Brookings Drive, Campus Box 1097, St Louis, MO, USA. sakiyama@wustl.edu.
Matthew J SilvaDepartment of Orthopedic Surgery, Washington University, 425 S Euclid, Box 8233, St Louis, MO, 63110, USA. silvam@wudosis.wustl.edu.
Shivam ShahDepartment of Orthopedic Surgery, Washington University, 425 S Euclid, Box 8233, St Louis, MO, 63110, USA. shivshah03@gmail.com.
Richard H GelbermanDepartment of Orthopedic Surgery, Washington University, 425 S Euclid, Box 8233, St Louis, MO, 63110, USA. gelberman@wudosis.wustl.edu.
Stavros ThomopoulosDepartment of Orthopedic Surgery, Washington University, 425 S Euclid, Box 8233, St Louis, MO, 63110, USA. ThomopoulosS@wudosis.wustl.edu.
Washington University in St. Louis · US

Funding

Enhanced Tendon Healing Through Growth Factor and Cell TherapiesR01AR062947 · NIAMS · WASHINGTON UNIVERSITY · PI GELBERMAN, RICHARD H, THOMOPOULOS, STAVROS · 2012 to 2022
$5.5M
Rotator Cuff Degeneration and RepairR01AR057836 · NIAMS · WASHINGTON UNIVERSITY · PI GALATZ, LEESA M, THOMOPOULOS, STAVROS · 2010 to 2020
$3.1M
Evaluating the Role of Inflammation in Tendinopathy with Transgenic MiceF31AR066452 · NIAMS · WASHINGTON UNIVERSITY · PI SHAH, SHIVAM · 2014 to 2016
$74k
NIAMS NIH HHS F31 AR066452NIAMS NIH HHS R01 AR057836NIAMS NIH HHS R01 AR062947
6 · The paper itself

Abstract

introductionMacrophage-driven inflammation is a key feature of the early period following tendon repair, but excessive inflammation has been associated with poor clinical outcomes. Modulation of the inflammatory environment using molecular or cellular treatments may provide a means to enhance tendon healing.

methodsTo examine the effect of pro-inflammatory cytokines secreted by macrophages on tendon fibroblasts (TF), we established in vitro models of cytokine and macrophage-induced inflammation. Gene expression, protein expression, and cell viability assays were used to examine TF responses. In an effort to reduce the negative effects of inflammatory cytokines on TFs, adipose-derived mesenchymal stromal cells (ASCs) were incorporated into the model and their ability to modulate inflammation was investigated.

resultsThe inflammatory cytokine interleukin 1 beta (IL-1β) and macrophages of varying phenotypes induced up-regulation of pro-inflammatory factors and matrix degradation factors and down-regulation of factors related to extracellular matrix formation by TFs in culture. ASCs did not suppress these presumably negative effects induced by IL-1β. However, ASC co-culture with M1 (pro-inflammatory) macrophages successfully suppressed the effects of M1 macrophages on TFs by inducing a phenotypic switch from a pro-inflammatory macrophage phenotype to an anti-inflammatory macrophage phenotype, thus resulting in exposure of TFs to lower levels of pro-inflammatory cytokines (e.g., IL-1β, tumor necrosis factor alpha (TNFα)).

conclusionsThese findings suggest that IL-1β and M1 macrophages are detrimental to tendon healing and that ASC-mediated modulation of the post-operative inflammatory response may be beneficial for tendon healing.

Indexed as

Adipose TissueAnimalsCell DifferentiationCells, CulturedCell SurvivalCytokinesFibroblastsInflammationInterleukin-1betaMacrophagesMaleMesenchymal Stem CellsMiceMice, Inbred C57BLTendonsWound HealingCytokinesIL1B protein, ratInterleukin-1beta

Identifiers

PMID25889287
PMCPMC4416344
OpenAlexW2126871758

What OpenQuestion holds

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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.