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Chondrogenic Differentiation of Human Adipose Tissue-Derived Stem Cells on PLCL/Fibrin Hybrid Scaffolds

Authors
Kim, Sang HeeJung, YoungmeeKim, Sang-HeonRhie, Jong WonKim, Young HaKim, Chul GeunKim, Soo Hyun
Issue Date
Mar-2009
Publisher
KOREAN TISSUE ENGINEERING REGENERATIVE MEDICINE SOC
Keywords
Poly(L-lactide-co-e-caprolactone); fibrin; hybrid scaffold; human adipose tissue-derived stem cells; chondrogenic differentiation
Citation
TISSUE ENGINEERING AND REGENERATIVE MEDICINE, v.6, no.1-3, pp.313 - 319
Indexed
SCIE
SCOPUS
KCI
OTHER
Journal Title
TISSUE ENGINEERING AND REGENERATIVE MEDICINE
Volume
6
Number
1-3
Start Page
313
End Page
319
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/177140
ISSN
1738-2696
Abstract
In cartilage tissue engineering, choosing on an appropriate cell source and a scaffold for cartilaginous tissue formation seriously influences the clinical application of an engineered cartilage. The purpose of this study is to investigate chondrogenic differentiation of human adipose tissue-derived stromal cells(hASCs) by hybridizing of fibrin gels for mimicking 3-dimensional environments of native cartilage and a poly(L-lactide-co-epsilon-caprolactone)(PLCL) scaffold. PLCL scaffolds with 85% porosity and 300-500 mu m pore size were fabricated by a gel-pressing method. For examining chondrogenic differentiation of hASCs, cells were mixed with 0.5% fibrin solutions and subsequently they were seeded onto PLCL scaffolds. After that, cell-scaffold constructs were implanted subcutaneously in nude mice for Lip to 8 weeks. Specimens were harvested after 8 weeks and analyzed. From in Vivo Studies, the constructs used with fibrin-PLCL hybrid scaffolds showed more depositions of cartilage-specific ECM components, such as GAGs and collagen type II, as compared to the constructs used with PLCL scaffolds alone. Furthermore, the constructs seeded with hASCs that were induced to chondrogenesis in vitro prior to implantation improved cartilage matrix deposition as compare to the constructs seeded with non-induced hASCs. These results indicated that the use of the fibrin gels-PLCL hybrid scaffold Could enhance chondrogenic differentiation of hASCs and cartilaginous tissue formation. Also, the induction for chondrogenesis of hASCs prior to implantation in vitro could affect cartilaginous tissue formation in vivo. In conclusion, the hybrid system which was fabricated with the inoculation of ASCs and fibrin gels onto a PLCL scaffold could be a meaningful system in cartilage tissue engineering.
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