Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2007-2-14
pubmed:abstractText
Besides their microbicidal functions, human beta-defensins (hBD) and LL-37 activate different immune and inflammatory cells, and their expression is enhanced in inflamed skin and cutaneous wound sites. To protect against pathogens, the skin produces antimicrobial peptides including hBDs and LL-37. Therefore, the aim of our study was to investigate whether hBDs participate in cutaneous inflammation and wound healing by inducing keratinocyte migration, proliferation, and production of proinflammatory cytokines/chemokines. We found that hBD-2, -3, and -4 but not hBD-1 stimulated human keratinocytes to increase their gene expression and protein production of IL-6, IL-10, IP-10, monocyte chemoattractant protein-1, macrophage inflammatory protein-3alpha, and RANTES. This stimulatory effect was markedly suppressed by pertussis toxin and U-73122, inhibitors for G protein and phospholipase C, respectively. We also demonstrated that hBDs elicited intracellular Ca2+ mobilization, and increased keratinocyte migration, and proliferation. In addition, these peptides induced phosphorylation of EGFR, signal transducer and activator of transcription (STAT)1, and STAT3, which are intracellular signaling molecules involved in keratinocyte migration and proliferation. In our study, inhibition of these molecules significantly reduced hBD-mediated keratinocyte migration and proliferation. In conclusion, this study provides evidence that human antimicrobial peptides may be involved in skin immunity through stimulating cytokine/chemokine production, and participate in wound healing by promoting keratinocyte migration and proliferation.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/1-(6-((3-methoxyestra-1,3,5(10)-trie..., http://linkedlifedata.com/resource/pubmed/chemical/Antimicrobial Cationic Peptides, http://linkedlifedata.com/resource/pubmed/chemical/CCL20 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL20, http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL5, http://linkedlifedata.com/resource/pubmed/chemical/Chemokines, http://linkedlifedata.com/resource/pubmed/chemical/Chemokines, CC, http://linkedlifedata.com/resource/pubmed/chemical/Cytokines, http://linkedlifedata.com/resource/pubmed/chemical/Estrenes, http://linkedlifedata.com/resource/pubmed/chemical/Macrophage Inflammatory Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Pyrrolidinones, http://linkedlifedata.com/resource/pubmed/chemical/beta-Defensins
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1523-1747
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
127
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
594-604
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:17068477-Antimicrobial Cationic Peptides, pubmed-meshheading:17068477-Cell Movement, pubmed-meshheading:17068477-Cell Proliferation, pubmed-meshheading:17068477-Chemokine CCL20, pubmed-meshheading:17068477-Chemokine CCL5, pubmed-meshheading:17068477-Chemokines, pubmed-meshheading:17068477-Chemokines, CC, pubmed-meshheading:17068477-Cytokines, pubmed-meshheading:17068477-Epidermis, pubmed-meshheading:17068477-Estrenes, pubmed-meshheading:17068477-Gene Expression Regulation, pubmed-meshheading:17068477-Humans, pubmed-meshheading:17068477-Inflammation, pubmed-meshheading:17068477-Keratinocytes, pubmed-meshheading:17068477-Macrophage Inflammatory Proteins, pubmed-meshheading:17068477-Pyrrolidinones, pubmed-meshheading:17068477-Signal Transduction, pubmed-meshheading:17068477-beta-Defensins
pubmed:year
2007
pubmed:articleTitle
Antimicrobial peptides human beta-defensins stimulate epidermal keratinocyte migration, proliferation and production of proinflammatory cytokines and chemokines.
pubmed:affiliation
Atopy (Allergy) Research Center, Juntendo University School of Medicine, Tokyo, Japan. francois@med.juntendo.ac.jp
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't