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Human keratinocyte growth and differentiation on acellular porcine dermal matrix in relation to wound healing potential
Robert Zajicek, Vaclav Mandys, Ondrej Mestak, Jan Sevcik, Radana Königova, Eva Matouskova
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural
Grantová podpora
NS10507
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
Directory of Open Access Journals
od 2001
Free Medical Journals
od 2000
PubMed Central
od 2000
Europe PubMed Central
od 2000
ProQuest Central
od 2012-01-01
Open Access Digital Library
od 2000-01-01 do 2012-01-02
Open Access Digital Library
od 2001-01-01
Open Access Digital Library
od 2011-01-01
Open Access Digital Library
od 2012-01-03
Medline Complete (EBSCOhost)
od 2012-01-01
Health & Medicine (ProQuest)
od 2012-01-01
Wiley-Blackwell Open Access Titles
od 2000
ROAD: Directory of Open Access Scholarly Resources
od 2001
PubMed
22629190
DOI
10.1100/2012/727352
Knihovny.cz E-zdroje
- MeSH
- extracelulární matrix metabolismus MeSH
- fibroblasty cytologie fyziologie MeSH
- hojení ran fyziologie MeSH
- keratinocyty cytologie fyziologie MeSH
- kultivované buňky MeSH
- lidé MeSH
- proliferace buněk MeSH
- řízená tkáňová regenerace přístrojové vybavení metody MeSH
- tkáňové inženýrství přístrojové vybavení metody MeSH
- tkáňové podpůrné struktury MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Research Support, N.I.H., Extramural MeSH
A number of implantable biomaterials derived from animal tissues are now used in modern surgery. Xe-Derma is a dry, sterile, acellular porcine dermis. It has a remarkable healing effect on burns and other wounds. Our hypothesis was that the natural biological structure of Xe-Derma plays an important role in keratinocyte proliferation and formation of epidermal architecture in vitro as well as in vivo. The bioactivity of Xe-Derma was studied by a cell culture assay. We analyzed growth and differentiation of human keratinocytes cultured in vitro on Xe-Derma, and we compared the results with formation of neoepidermis in the deep dermal wounds treated with Xe-Derma. Keratinocytes cultured on Xe-Derma submerged in the culture medium achieved confluence in 7-10 days. After lifting the cultures to the air-liquid interface, the keratinocytes were stratified and differentiated within one week, forming an epidermis with basal, spinous, granular, and stratum corneum layers. Immunohistochemical detection of high-molecular weight cytokeratins (HMW CKs), CD29, p63, and involucrin confirmed the similarity of organization and differentiation of the cultured epidermal cells to the normal epidermis. The results suggest that the firm natural structure of Xe-Derma stimulates proliferation and differentiation of human primary keratinocytes and by this way improves wound healing.
Department of Pathology 3rd Faculty of Medicine Charles University Prague Prague Czech Republic
Prague Burn Centre 3rd Faculty of Medicine Charles University Prague Prague Czech Republic
Prague Burn Centre University Hospital Kralovske Vinohrady Prague Czech Republic
Citace poskytuje Crossref.org
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