Evidence map›Paper›PMID 25584990›Full record

ArticleActa biomaterialia2015

Collagen-gelatin mixtures as wound model, and substrates for VEGF-mimetic peptide binding and endothelial cell activation.

Tania R Chan, Patrick J Stahl, Yang Li, S Michael Yu

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  14. Targeting collagen for diagnostic imaging and therapeutic delivery.Journal of controlled release : official journal of the Controlled Release Society · 2016
    Review
  15. Taking cues from the extracellular matrix to design bone-mimetic regenerative scaffolds.Matrix biology : journal of the International Society for Matrix Biology
    Review
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

4 authors at 2 institutions in 1 country.

Tania R ChanDepartment of Materials Science and Engineering, The Johns Hopkins University, 3400 N. Charles St, Baltimore, MD 21218, USA.
Patrick J StahlDepartment of Materials Science and Engineering, The Johns Hopkins University, 3400 N. Charles St, Baltimore, MD 21218, USA.
Yang LiDepartment of Bioengineering, University of Utah, 36 S Wasatch Drive, 3100 SMBB, Salt Lake City, UT 84112, USA.
S Michael YuDepartment of Bioengineering, University of Utah, 36 S Wasatch Drive, 3100 SMBB, Salt Lake City, UT 84112, USA. Electronic address: michael.yu@utah.edu.
Johns Hopkins University · USUniversity of Utah · US

Funding

Study and Application of Collagen Mimetic Peptide-Collagen HybridizationR01AR060484 · NIAMS · UNIVERSITY OF UTAH · PI YU, MICHAEL S · 2011 to 2015
$1.7M
Collagen-Targeted Therapeutics of Cathepsin InhibitorsR21AR065124 · NIAMS · UNIVERSITY OF UTAH · PI YU, MICHAEL S · 2014 to 2015
$381k
Howard Hughes Medical InstituteNIAMS NIH HHS R01 AR060484NIAMS NIH HHS R01AR060484NIAMS NIH HHS R21 AR065124NIAMS NIH HHS R21AR065124
6 · The paper itself

Abstract

In humans, high level of collagen remodeling is seen during normal physiological events such as bone renewal, as well as in pathological conditions, such as arthritis, tumor growth and other chronic wounds. Our lab recently discovered that collagen mimetic peptide (CMP) is able to hybridize with denatured collagens at these collagen remodeling sites with high affinity. Here, we show that the CMP's high binding affinity to denatured collagens can be utilized to deliver angiogenic signals to scaffolds composed of heat-denatured collagens (gelatins). We first demonstrate hybridization between denatured collagens and QKCMP, a CMP with pro-angiogenic QK domain. We show that high levels of QKCMP can be immobilized to a new artificial matrix containing both fibrous type I collagen and heat denatured collagen through triple helix hybridization, and that the QKCMP is able to stimulate early angiogenic response of endothelial cells (ECs). We also show that the QKCMP can bind to excised tissues from burn injuries in cutaneous mouse model, suggesting its potential for promoting neovascularization of burn wounds.

Indexed as

Amino Acid SequenceAnimalsBurnsCattleCollagen Type IFluorescenceGelatinHumansHuman Umbilical Vein Endothelial CellsMiceMolecular Sequence DataMolecular WeightPeptidesProtein BindingProtein DenaturationRatsCollagen Type IGelatinPeptidesVascular Endothelial Growth Factor AAngiogenesisCollagenMicrovasculatureTissue engineeringVEGF

Identifiers

PMID25584990
PMCPMC4404521
OpenAlexW2091950308

What OpenQuestion holds

Textmetadata
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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.