Evidence map›Paper›PMID 28646271›Full record

ArticleStem cell reviews and reports2017

Characterization of Adipose-Derived Stem Cells Following Burn Injury.

Anesh Prasai, Amina El Ayadi, Randy C Mifflin, Michael D Wetzel, Clark R Andersen, Heinz Redl, David N Herndon, Celeste C Finnerty

Open access · hybridAbstract read
In one paragraph

Article in Stem cell reviews and reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Adipose tissue: a neglected organ in the response to severe trauma?Cellular and molecular life sciences : CMLS · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Skin tissue regeneration for burn injury.Stem cell research & therapy · 2019
    Review
  12. 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

8 authors at 3 institutions in 2 countries.

Anesh PrasaiCell Biology Graduate Program, University of Texas Medical Branch, Galveston, TX, USA.
Amina El AyadiDepartment of Surgery, University of Texas Medical Branch, Galveston, TX, USA.
Randy C MifflinDepartment of Surgery, University of Texas Medical Branch, Galveston, TX, USA.
Michael D WetzelCell Biology Graduate Program, University of Texas Medical Branch, Galveston, TX, USA.
Clark R AndersenDepartment of Surgery, University of Texas Medical Branch, Galveston, TX, USA.
Heinz RedlLudwig Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.
David N HerndonDepartment of Surgery, University of Texas Medical Branch, Galveston, TX, USA.
Celeste C FinnertyDepartment of Surgery, University of Texas Medical Branch, Galveston, TX, USA. ccfinner@utmb.edu.
The University of Texas Medical Branch at Galveston · USLudwig Boltzmann Institute for Experimental and Clinical Traumatology · ATShriners Hospitals for Children - Galveston · US

Funding

Project 9: The role of androgen/corticosteroid in fat, muscle and glucose metabolism of burn victimsP50GM060338 · NIGMS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI HERNDON, DAVID N. · 2000 to 2017
$24.2M
UTMB Clinical and Translational Science AwardUL1TR000071 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BRASIER, ALLAN R. · 2012 to 2014
$14.4M
MODULATION OF THE POSTBURN HYPERMETABOLIC RESPONSER01GM056687 · NIGMS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI HERNDON, DAVID N. · 1998 to 2017
$9.0M
Effects of Chronic Catecholamine Exposure on Post-burn ScarringR01GM112936 · NIGMS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI FINNERTY, CELESTE CAMPBELL · 2015 to 2019
$1.8M
Anderson Foundation NoneGillson Longenbaugh Foundation NoneNational Institute of General Medical Sciences P50GM060338National Institute of General Medical Sciences R01GM056687National Institutes of Health UL1TR000071NCATS NIH HHS UL1 TR000071NIGMS NIH HHS P50 GM060338NIGMS NIH HHS R01 GM056687NIGMS NIH HHS R01 GM112936Shriners of North America 80500Shriners of North America 84202
6 · The paper itself

Abstract

Severe burns induce a prolonged inflammatory response in subcutaneous adipose tissue that modulates signaling in adipose-derived stem cells (ASCs), which hold potential for healing burn wounds or generating skin substitutes. Using a 60% rat scald burn model, we conducted a series of experiments to determine which cells isolated from the adipose tissue produced inflammatory mediators and how these changes affect ASC fate and function. The stromal vascular fraction (SVF), adipocytes, and ASCs were isolated from adipose tissue at varying times up to 4 weeks postburn and from non-injured controls. Endpoints included inflammatory marker expression, expression of ASC-specific cell-surface markers, DNA damage, differentiation potential, and proliferation. Inflammatory marker expression was induced in adipocytes and the SVF at 24 and 48 h postburn; expression of inflammatory marker mRNA transcripts and protein returned to normal in the SVF isolated 1 week postburn. In enriched ASCs, burns did not alter cell-surface expression of stem cell markers, markers of inflammation, differentiation potential, or proliferative ability. These results suggest that adipocytes and the SVF produce large quantities of inflammatory mediators, but that ASCs do not, after burns and that ASCs are unaffected by burn injury or culturing procedures.. They also suggest that cells isolated over 48 h after injury are best for cell culture or tissue engineering purposes.

Indexed as

AdipocytesAdipose TissueAnimalsBurnsCell DifferentiationCell ProliferationHumansMesenchymal Stem CellsRatsStem CellsTissue EngineeringVascular GraftingWound HealingAdipocytesAdipose-derived stem cellAdipose tissueBurnsInflammationStromal vascular fraction

Identifiers

PMID28646271
PMCPMC5730636
OpenAlexW2690794406

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.