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Chondrogenic differentiation of human bone marrow and adipose tissue-derived mesenchymal stem cells
Ľuboš Danišovič, Petr Lesný, Vojtěch Havlas, Petr Teyssler, Zdeňka Syrová, Martin Kopáni, Gabriela Fujeríková, Tomáš Trč, Eva Syková, Pavla Jendelová
Jazyk angličtina Země Česko
Grantová podpora
NR8121
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Část
Zdroj
NLK
Free Medical Journals
od 2003 do 2013
Freely Accessible Science Journals
od 2003 do 2013
ROAD: Directory of Open Access Scholarly Resources
od 2002
- MeSH
- finanční podpora výzkumu jako téma MeSH
- imunohistochemie metody využití MeSH
- kloubní chrupavka abnormality patologie růst a vývoj MeSH
- kolagen typ II fyziologie genetika MeSH
- kostní dřeň fyziologie chirurgie MeSH
- kultivované buňky fyziologie transplantace MeSH
- lidé MeSH
- mezenchymální kmenové buňky fyziologie MeSH
- polymerázová řetězová reakce s reverzní transkripcí metody využití MeSH
- transformující růstový faktor beta1 terapeutické užití MeSH
- tuková tkáň fyziologie chirurgie MeSH
- Check Tag
- lidé MeSH
Congenital abnormalities, various diseases and injuries may result in the degeneration of articular cartilage. Recently, stem cell therapy has offered new treatment possibilities for this condition. The aim of our study was to verify the chondrogenic differentiation potential of human bone marrow mesenchymal stem cells (BMSCs) and adipose tissue-derived mesenchymal stem cells (AMSCs) in vitro in the presence or absence of transforming growth factor beta (TGF-beta1). Human BMSCs and AMSCs from healthy donors were collected during orthopaedic surgeries and expanded in vitro to obtain a sufficient quantity of cells; their chondrogenic differentiation was studied in the pellet culture system. Spontaneous chondrogenesis occurred in both BMSC and AMSC pellet cultures and was similar in both TGF-beta1 treated and untreated pellet cultures. BMSC pellets contained more cells with a chondrogenic phenotype. The presence of TGF-beta1 led to a decrease in the levels of collagen type I mRNA and to increased levels of collagen type II mRNA only in the BMSC pellet culture. Our results demonstrate that although both mesenchymal cell types can be used in cartilage tissue engineering, the chondrogenic potential of human BMSCs is higher than that of AMSCs.
Citace poskytuje Crossref.org
Grant č. NR 8121 IGA MZČR
Bibliografie atd.Lit.: 33
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- $a Congenital abnormalities, various diseases and injuries may result in the degeneration of articular cartilage. Recently, stem cell therapy has offered new treatment possibilities for this condition. The aim of our study was to verify the chondrogenic differentiation potential of human bone marrow mesenchymal stem cells (BMSCs) and adipose tissue-derived mesenchymal stem cells (AMSCs) in vitro in the presence or absence of transforming growth factor beta (TGF-beta1). Human BMSCs and AMSCs from healthy donors were collected during orthopaedic surgeries and expanded in vitro to obtain a sufficient quantity of cells; their chondrogenic differentiation was studied in the pellet culture system. Spontaneous chondrogenesis occurred in both BMSC and AMSC pellet cultures and was similar in both TGF-beta1 treated and untreated pellet cultures. BMSC pellets contained more cells with a chondrogenic phenotype. The presence of TGF-beta1 led to a decrease in the levels of collagen type I mRNA and to increased levels of collagen type II mRNA only in the BMSC pellet culture. Our results demonstrate that although both mesenchymal cell types can be used in cartilage tissue engineering, the chondrogenic potential of human BMSCs is higher than that of AMSCs.
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