Effects of a chitosan scaffold containing TGF-beta 1 encapsulated chitosan microspheres on in vitro chondrocyte culture

Authors
Lee, JEKim, SEKwon, ICAhn, HJCho, HLee, SHKim, HJSeong, SCLee, MC
Issue Date
2004-09
Publisher
WILEY
Citation
ARTIFICIAL ORGANS, v.28, no.9, pp.829 - 839
Abstract
The objectives of this study were (1) to develop a three-dimensional chitosan scaffold in combination with transforming growth factor-beta1 (TGF-beta1)-loaded chitosan microspheres and (2) to evaluate the effect of the TGF-beta1 release on the chondrogenic potential of rabbit chondrocytes in the scaffolds. TGF-beta1 was loaded into chitosan microspheres using an emulsion-crosslinking method, resulting in spherical shapes with a size ranging from 0.3 to 1.5 mum. Controlled release of TGF-beta1, as measured by enzyme-linked immunosorbent assay (ELISA), was observed with chitosan microspheres over 7 days. Chitosan solutions (2% and 3%) were fabricated into two types of scaffolds with different pore morphologies and mechanical properties using a freeze-drying technique, with the result that scaffold with higher concentrations showed smaller pores and lower porosity, leading to a much stronger scaffold. The TGF-beta1 microspheres were incorporated into the scaffolds at a concentration of 10 ng TGF-beta1/scaffold and then chondrocytes seeded into each scaffold and incubated in vitro for 2 weeks. The 2% chitosan scaffolds showed higher cell attachment levels than the 3% chitosan scaffolds (P < 0.01), regardless of the TGF-beta1 microspheres. Both the proliferation rate and glycosaminoglycan (GAG) production were significantly higher for scaffolds incorporating TGF-beta1 microspheres than for the control scaffolds without microspheres 10 days after incubation. Extracellular matrix staining by Safranin O and immunohistochemistry for type II collagen both significantly increased in scaffolds containing TGF-beta1 microspheres. These results suggest that the TGF-beta1 microsphere incorporated in scaffolds have the potential to enhance cartilage formation.
Keywords
GROWTH-FACTOR BETA-1; ARTICULAR-CARTILAGE; CONTROLLED-RELEASE; GENE DELIVERY; MATRIX; OSTEOBLASTS; HYDROGEL; GROWTH-FACTOR BETA-1; ARTICULAR-CARTILAGE; CONTROLLED-RELEASE; GENE DELIVERY; MATRIX; OSTEOBLASTS; HYDROGEL; chitosan; scaffold; chondrocyte; tissue engineering; cartilage; microsphere; growth factor; controlled release
ISSN
0160-564X
URI
https://pubs.kist.re.kr/handle/201004/137290
DOI
10.1111/j.1525-1594.2004.00020.x
Appears in Collections:
KIST Article > 2004
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