Evidence map›Paper›PMID 38867276›Full record

ArticleStem cell research & therapy2024

Inhibition and reversal of a TGF-β1 induced myofibroblast phenotype by adipose tissue-derived paracrine factors.

S Higginbotham, V L Workman, A-V Giblin, N H Green, D W Lambert, V Hearnden

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Article in Stem cell research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

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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

6 authors.

S HigginbothamDepartment of Materials Science and Engineering, University of Sheffield, Sheffield, UK. samhigginbotham98@gmail.com.ORCID 0000-0002-6017-3507
V L WorkmanDepartment of Materials Science and Engineering, University of Sheffield, Sheffield, UK.ORCID 0000-0002-9135-8993
A-V GiblinDepartment of Plastic Surgery, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.ORCID 0000-0002-6593-9831
N H GreenDepartment of Materials Science and Engineering, University of Sheffield, Sheffield, UK.ORCID 0000-0001-5413-0642
D W LambertSchool of Clinical Dentistry, University of Sheffield, Sheffield, UK.ORCID 0000-0001-9003-3145
V HearndenDepartment of Materials Science and Engineering, University of Sheffield, Sheffield, UK.ORCID 0000-0003-0838-7783

Funding

EPSRC Doctoral Training Programme Scholarship EP/R513313/1
6 · The paper itself

Abstract

backgroundHypertrophic scarring results from myofibroblast differentiation and persistence during wound healing. Currently no effective treatment for hypertrophic scarring exists however, autologous fat grafting has been shown to improve scar elasticity, appearance, and function. The aim of this study was to understand how paracrine factors from adipose tissues and adipose-derived stromal cells (ADSC) affect fibroblast to myofibroblast differentiation.

methodsThe transforming growth factor-β1 (TGF-β1) induced model of myofibroblast differentiation was used to test the effect of conditioned media from adipose tissue, ADSC or lipid on the proportion of fibroblasts and myofibroblasts.

resultsAdipose tissue conditioned media inhibited the differentiation of fibroblasts to myofibroblasts but this inhibition was not observed following treatment with ADSC or lipid conditioned media. Hepatocyte growth factor (HGF) was readily detected in the conditioned medium from adipose tissue but not ADSC. Cells treated with HGF, or fortinib to block HGF, demonstrated that HGF was not responsible for the inhibition of myofibroblast differentiation. Conditioned media from adipose tissue was shown to reduce the proportion of myofibroblasts when added to fibroblasts previously treated with TGF-β1, however, conditioned media treatment was unable to significantly reduce the proportion of myofibroblasts in cell populations isolated from scar tissue.

conclusionsCultured ADSC or adipocytes have been the focus of most studies, however, this work highlights the importance of considering whole adipose tissue to further our understanding of fat grafting. This study supports the use of autologous fat grafts for scar treatment and highlights the need for further investigation to determine the mechanism.

Indexed as

Adipose TissueCell DifferentiationHepatocyte Growth FactorMyofibroblastsTransforming Growth Factor beta1AdipocytesCells, CulturedCulture Media, ConditionedFibroblastsHumansParacrine CommunicationPhenotypeStromal CellsCulture Media, ConditionedHepatocyte Growth FactorTransforming Growth Factor beta1Adipose-derived stromal cellsAutologous fat graftingMyofibroblastsScarringTransforming growth factor β-1

Identifiers

PMID38867276
PMCPMC11170827

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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.