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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
Language English Country Czech Republic
Grant support
NR8121
MZ0
CEP Register
Digital library NLK
Full text - Část
Source
NLK
Free Medical Journals
from 2003 to 2013
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from 2003 to 2013
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from 2002
- MeSH
- Research Support as Topic MeSH
- Immunohistochemistry methods utilization MeSH
- Cartilage, Articular abnormalities pathology growth & development MeSH
- Collagen Type II physiology genetics MeSH
- Bone Marrow physiology surgery MeSH
- Cells, Cultured physiology transplantation MeSH
- Humans MeSH
- Mesenchymal Stem Cells physiology MeSH
- Reverse Transcriptase Polymerase Chain Reaction methods utilization MeSH
- Transforming Growth Factor beta1 therapeutic use MeSH
- Adipose Tissue physiology surgery MeSH
- Check Tag
- Humans 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.
References provided by Crossref.org
Grant č. NR 8121 IGA MZČR
Bibliography, etc.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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