Evidence map›Paper›PMID 28820426›Full record

ArticleInternational journal of molecular sciences2017

Burn Eschar Stimulates Fibroblast and Adipose Mesenchymal Stromal Cell Proliferation and Migration but Inhibits Endothelial Cell Sprouting.

Hanneke N Monsuur, Lenie J van den Broek, Renushka L Jhingoerie, Adrianus F P M Vloemans, Susan Gibbs

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Recent Advances in Scar Biology.International journal of molecular sciences · 2018
    Article
  9. Nanoparticle-functionalized dressings for the treatment of third-degree skin burns - histopathological and immunohistochemical study.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Article
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

5 authors at 3 institutions in 1 country.

Hanneke N MonsuurDepartment of Dermatology, VU University Medical Center, Amsterdam Movement Sciences, 1081 HZ Amsterdam, The Netherlands. h.monsuur@vumc.nl.
Lenie J van den BroekDepartment of Dermatology, VU University Medical Center, Amsterdam Movement Sciences, 1081 HZ Amsterdam, The Netherlands. l.vandenbroek@vumc.nl.
Renushka L JhingoerieDepartment of Dermatology, VU University Medical Center, Amsterdam Movement Sciences, 1081 HZ Amsterdam, The Netherlands. renushkajhingoerie@gmail.com.
Adrianus F P M VloemansBurn Center, Red Cross Hospital, 1942 LE Beverwijk, The Netherlands. jvloemans@rkz.nl.
Susan GibbsDepartment of Dermatology, VU University Medical Center, Amsterdam Movement Sciences, 1081 HZ Amsterdam, The Netherlands. s.gibbs@vumc.nl.
Amsterdam UMC Location Vrije Universiteit Amsterdam · NLAcademic Center for Dentistry Amsterdam · NLAssociation of Dutch Burn Centres · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The majority of full-thickness burn wounds heal with hypertrophic scar formation. Burn eschar most probably influences early burn wound healing, since granulation tissue only forms after escharotomy. In order to investigate the effect of burn eschar on delayed granulation tissue formation, burn wound extract (BWE) was isolated from the interface between non-viable eschar and viable tissue. The influence of BWE on the activity of endothelial cells derived from dermis and adipose tissue, dermal fibroblasts and adipose tissue-derived mesenchymal stromal cells (ASC) was determined. It was found that BWE stimulated endothelial cell inflammatory cytokine (CXCL8, IL-6 and CCL2) secretion and migration. However, BWE had no effect on endothelial cell proliferation or angiogenic sprouting. Indeed, BWE inhibited basic Fibroblast Growth Factor (bFGF) induced endothelial cell proliferation and sprouting. In contrast, BWE stimulated fibroblast and ASC proliferation and migration. No difference was observed between cells isolated from dermis or adipose tissue. The inhibitory effect of BWE on bFGF-induced endothelial proliferation and sprouting would explain why excessive granulation tissue formation is prevented in full-thickness burn wounds as long as the eschar is still present. Identifying the eschar factors responsible for this might give indications for therapeutic targets aimed at reducing hypertrophic scar formation which is initiated by excessive granulation tissue formation once eschar is removed.

Indexed as

Adipose TissueAdultAgedBurnsCell MovementCell ProliferationCicatrix, HypertrophicCytokinesDermisEndothelial CellsFemaleFibroblast Growth Factor 2FibroblastsHumansMaleMesenchymal Stem CellsCytokinesFibroblast Growth Factor 2Tissue ExtractsASCburnendothelial cellfibroblastgranulation tissueskinwound extractwound healing

Identifiers

PMID28820426
PMCPMC5578178
OpenAlexW2749320522

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.