Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2008-9-15
pubmed:abstractText
Acceleration of the wound healing process by using angiogenic peptides has been demonstrated previously. Here we used select laminin-111 peptides, A13 and C16, from the laminin alpha1 and gamma1 chain, respectively, to test whether they are able to stimulate wound healing in a rat full thickness wound model. The 12-mer peptides C16 and A13 are highly angiogenic and bind to integrins alphavbeta3 and alpha5beta1. We show that A13 increases wound re-epithelialization as much as 17% over controls by day 4 and C16 increases coverage by 11%. Contraction of the treated wounds was increased as much as 11% for A13 and 8% for C16 at day 4. No differences were observed at day 7 with either peptide. The peptides also stimulated fibroblast migration in Boyden chamber assays. A13 increased cell migration as much as 2.4-fold on uncoated filters and as much as 16-fold on collagen type IV-coated filters over negative controls. Similarly, C16 also stimulated migration 1.8-fold on uncoated filters and as much as 12-fold on collagen-coated filters. A13 and C16 significantly decreased expression of the pro and active forms of matrix metalloproteinase 2 in foreskin fibroblasts indicating their role in collagen accumulation. We conclude that small bioactive angiogenic peptides can promote dermal wound healing and may offer a new class of stable and chemically manipulable therapeutics for wound healing.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-10189356, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-10564562, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-10697171, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-10978889, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-11083552, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-12706114, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-12714040, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-1279183, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-12809772, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-1297987, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-1376557, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-15225204, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-1524367, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-15541073, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-1569118, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-15979864, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-15993569, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-17194893, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-17276196, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-1734035, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-17719208, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-2071570, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-2491959, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-7823364, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-8447113, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-8841427, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-8867813, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-8908195, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-8930117, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-9105037, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-9194528, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-9211848, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-9232815, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-9410218, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-9531563, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-9551940, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-9645941, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-9665817, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-9777972, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-9852164, http://linkedlifedata.com/resource/pubmed/commentcorrection/18603014-9872929
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1357-2725
pubmed:author
pubmed:issnType
Print
pubmed:volume
40
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2771-80
pubmed:dateRevised
2011-9-26
pubmed:meshHeading
pubmed-meshheading:18603014-Angiogenic Proteins, pubmed-meshheading:18603014-Animals, pubmed-meshheading:18603014-Cell Movement, pubmed-meshheading:18603014-Cells, Cultured, pubmed-meshheading:18603014-Collagen Type IV, pubmed-meshheading:18603014-Dose-Response Relationship, Drug, pubmed-meshheading:18603014-Endothelium, pubmed-meshheading:18603014-Endothelium, Vascular, pubmed-meshheading:18603014-Fibroblasts, pubmed-meshheading:18603014-Humans, pubmed-meshheading:18603014-Integrin alpha5beta1, pubmed-meshheading:18603014-Integrin alphaVbeta3, pubmed-meshheading:18603014-Laminin, pubmed-meshheading:18603014-Matrix Metalloproteinase 2, pubmed-meshheading:18603014-Neovascularization, Physiologic, pubmed-meshheading:18603014-Rats, pubmed-meshheading:18603014-Skin, pubmed-meshheading:18603014-Time Factors, pubmed-meshheading:18603014-Umbilical Veins, pubmed-meshheading:18603014-Wound Healing
pubmed:year
2008
pubmed:articleTitle
Angiogenic laminin-derived peptides stimulate wound healing.
pubmed:affiliation
Review Branch DERA, NHLBI, NIH, Bethesda, MD 20892-1857, USA.
pubmed:publicationType
Journal Article