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Chondrogenesis of human bone marrow mesenchymal cells by transforming growth factors β1 through cell shape changes on controlled biomaterials
Journal of biomedical materials research. Part A, 2012-12, Vol.100A (12), p.3344-3352
Shao, Hung-Jen
Ho, Chia-Chi
Lee, Yu-Tsang
Chen, Chiang-Sang
Wang, Jyh-Horng
Young, Tai-Horng
2012
Details
Autor(en) / Beteiligte
Shao, Hung-Jen
Ho, Chia-Chi
Lee, Yu-Tsang
Chen, Chiang-Sang
Wang, Jyh-Horng
Young, Tai-Horng
Titel
Chondrogenesis of human bone marrow mesenchymal cells by transforming growth factors β1 through cell shape changes on controlled biomaterials
Ist Teil von
Journal of biomedical materials research. Part A, 2012-12, Vol.100A (12), p.3344-3352
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
2012
Link zum Volltext
Quelle
Wiley Online Library
Beschreibungen/Notizen
The phenotypic responses of human bone marrow mesenchymal cells (hBMSCs) on different ratio of chitosan/polycaprolactone (PCL) blends were investigated in this study. The results showed that hBMSCs existed different morphology on chitosan/PCL blends due to the different adhesion characteristic of cell on neat PCL and neat chitosan. Interestingly, comparing to hBMSCs on neat PCL, hBMSCs aggregated to form spheroid and to express ascendant trend of transforming growth factor β1, collagen type II, collagen type X, and Sox9 mRNA on the chitosan/PCL blended substrates with the decrease of PCL content. To confirm chondrogenesis of hBMSCs with spheroid on test substrates, Alcian Blue and Safranin O staining were used to detect the cartilaginous extracellular matrix (ECM). It revealed hBMSCs with spheroid on neat chitosan and 10 wt % PCL did turn to chondrogenic differentiation and synthesize cartilaginous ECM. Therefore, these findings provided new insights into the role of chitosan/PCL blended material could mediate the endogenous gene expression of hBMSCs to alter the phenotypic behavior through mediating the cell shape. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 100A:3344–3352, 2012.
Sprache
Englisch
Identifikatoren
ISSN: 1549-3296
eISSN: 1552-4965
DOI: 10.1002/jbm.a.34291
Titel-ID: cdi_proquest_miscellaneous_1114950610
Format
–
Schlagworte
Actins - metabolism
,
Adult
,
Biocompatible Materials - pharmacology
,
Biological and medical sciences
,
Biomaterials
,
Biomedical materials
,
blends
,
Bone biomaterials
,
Bone marrow
,
Bone Marrow Cells - cytology
,
Bone Marrow Cells - drug effects
,
Bone Marrow Cells - metabolism
,
Bone Marrow Cells - ultrastructure
,
Cartilage - drug effects
,
Cartilage - metabolism
,
Cell Proliferation - drug effects
,
Cell Shape - drug effects
,
Cell size
,
Cells, Cultured
,
Chitosan
,
Chondrogenesis
,
Chondrogenesis - drug effects
,
Collagen
,
Collagen (type II)
,
Cytoskeleton - drug effects
,
Cytoskeleton - metabolism
,
Extracellular matrix
,
Extracellular Matrix - drug effects
,
Extracellular Matrix - metabolism
,
Gene expression
,
Gene Expression Regulation - drug effects
,
Growth factors
,
human bone marrow mesenchymal cells
,
Humans
,
Medical sciences
,
Mesenchymal Stromal Cells - cytology
,
Mesenchymal Stromal Cells - drug effects
,
Mesenchymal Stromal Cells - metabolism
,
Mesenchymal Stromal Cells - ultrastructure
,
Mesenchyme
,
Middle Aged
,
Mixtures
,
Morphology
,
Polycaprolactone
,
RNA, Messenger - genetics
,
RNA, Messenger - metabolism
,
Sox9 protein
,
Substrates
,
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
,
Technology. Biomaterials. Equipments
,
Transforming Growth Factor beta1 - antagonists & inhibitors
,
Transforming Growth Factor beta1 - genetics
,
Transforming Growth Factor beta1 - metabolism
,
transforming growth factor β1
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