Bioactive polymer/extracellular matrix scaffolds fabricated with a flow perfusion bioreactor for cartilage tissue engineering.
Bioactive polymer/extracellular matrix scaffolds fabricated with a flow perfusion bioreactor for cartilage tissue engineering.
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DOI:
10.1016/j.biomaterials.2010.07.110
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发表时间:
2010-12
期刊:
影响因子:
14
通讯作者:
Mikos, Antonios G.
中科院分区:
文献类型:
--
作者:
Liao, Jiehong;Guo, Xuan;Grande-Allen, K. Jane;Kasper, F. Kurtis;Mikos, Antonios G.
关键词:
In this study, electrospun poly(ε-caprolactone) (PCL) microfiber scaffolds, coated with cartilaginous extracellular matrix (ECM), were fabricated by first culturing chondrocytes under dynamic conditions in a flow perfusion bioreactor and then decellularizing the cellular constructs. The decellularization procedure yielded acellular PCL/ECM composite scaffolds containing glycosaminoglycan and collagen. PCL/ECM composite scaffolds were evaluated for their ability to support the chondrogenic differentiation of mesenchymal stem cells (MSCs) in vitro using serum-free medium with or without the addition of transforming growth factor-β1 (TGF-β1). PCL/ECM composite scaffolds supported chondrogenic differentiation induced by TGF-β1 exposure, as evidenced in the up-regulation of aggrecan (11.6 ± 3.8 fold) and collagen type II (668.4 ± 317.7 fold) gene expression. The presence of cartilaginous matrix alone reduced collagen type I gene expression to levels observed with TGF-β1 treatment. Cartilaginous matrix further enhanced the effects of growth factor treatment on MSC chondrogenesis as evidenced in the higher glycosaminoglycan synthetic activity for cells cultured on PCL/ECM composite scaffolds. Therefore, flow perfusion culture of chondrocytes on electrospun microfiber scaffolds is a promising method to fabricate polymer/extracellular matrix composite scaffolds that incorporate both natural and synthetic components to provide biological signals for cartilage tissue engineering applications.
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影响因子:
9.7
作者:
Liao, Jiehong;Guo, Xuan;Nelson, Dan;Kasper, F. Kurtis;Mikos, Antonios G.
通讯作者:
Mikos, Antonios G.
影响因子:
--
作者:
Farrell, E;O'Brien, FJ;Campbell, VA
通讯作者:
Campbell, VA
影响因子:
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作者:
Gomes, ME;Bossano, CM;Mikos, AG
通讯作者:
Mikos, AG
影响因子:
14
作者:
Li, WJ;Tuli, R;Tuan, RS
通讯作者:
Tuan, RS
影响因子:
14
作者:
Hu, JC;Athanasiou, KA
通讯作者:
Athanasiou, KA