Evidence map›Paper›PMID 24126844›Full record

ArticleThe Journal of investigative dermatology2014

Fibronectin peptides that bind PDGF-BB enhance survival of cells and tissue under stress.

Fubao Lin, Jia Zhu, Marcia G Tonnesen, Breena R Taira, Steve A McClain, Adam J Singer, Richard A F Clark

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.8field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 39 citations in OpenAlex.

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  7. Extracellular matrix-derived peptides in tissue remodeling and fibrosis.Matrix biology : journal of the International Society for Matrix Biology · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Fubao LinDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York, USA.
Jia ZhuDepartments of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, USA.
Marcia G TonnesenDepartment of Dermatology, Stony Brook University, Stony Brook, New York, USA; Department of Medicine, Northport VA Medical Center, Northport, New York, USA.
Breena R TairaOlive View-UCLA Medical Center, Sylmar, California, USA.
Steve A McClainDepartment of Emergency Medicine, Stony Brook University, Stony Brook, New York, USA.
Adam J SingerDepartment of Emergency Medicine, Stony Brook University, Stony Brook, New York, USA.
Richard A F ClarkDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York, USA; Department of Dermatology, Stony Brook University, Stony Brook, New York, USA. Electronic address: richard.clark@stonybrook.edu.
Stony Brook University · USNorthport VA Medical Center · USOlive View-UCLA Medical Center · US

Funding

FIBRONECTIN AND CELL RECRUITMENTR37AG010143 · NIA · STATE UNIVERSITY NEW YORK STONY BROOK · PI CLARK, RICHARD AUGUST · 1996 to 2005
$2.4M
Novel peptide to inhibit burn injury progressionRC2AR059384 · NIAMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI CLARK, RICHARD AUGUST, SINGER, ADAM JOHN · 2009 to 2010
$1.7M
NIAMS NIH HHS RC2 AR059384NIA NIH HHS R37 AG010143PHS HHS NA10143
6 · The paper itself

Abstract

Stressors after injury from a multitude of factors can lead to cell death. We have identified four fibronectin (FN) peptides: two from the first FN type III repeat (FNIII1), one from the 13th FN type III repeat (FNIII13), and one from FN variable region (IIICS), which when tethered to a surface acted as platelet-derived growth factor-BB (PDGF-BB) enhancers to promote cell survival. One of the FNIII1 peptides and its smallest (14-mer) bioactive form (P12) were also active in solution. Specifically, P12 bound PDGF-BB (KD=200 nM), enhanced adult human dermal fibroblast (AHDF) survival under serum starvation, oxidative or endoplasmic reticulum stressors, and limited burn-injury progression in a rat hot comb model. Furthermore, P12 inhibited endoplasmic reticulum stress-induced c-Jun N-terminal kinase (JNK) activation. Although many growth factors have been found to bind FN directly or indirectly, here we identify peptide sequences of growth factor-binding sites in FN. The finding of these peptides further delineated how the extracellular matrix protein FN can support cell survival. As the peptide P12 is active in either soluble form or tethered to a substrate, it will have multifactorial uses as a bioactive peptide by itself or in tissue engineering.

Indexed as

Cell SurvivalAnimalsApoptosisBecaplerminBinding SitesBurnsCells, CulturedDisease ProgressionEndoplasmic Reticulum StressFibroblastsFibronectinsHumansIntercellular Signaling Peptides and ProteinsMiceOxygenPeptidesBecaplerminFibronectinsIntercellular Signaling Peptides and ProteinsOxygenPeptidesProto-Oncogene Proteins c-sis

Identifiers

PMID24126844
PMCPMC3961564
OpenAlexW1987710329

What OpenQuestion holds

Textmetadata
LicenceTDM
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.