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Effects of an Avidin-Biotin Binding System on Chondrocyte Adhesion and Growth on Biodegradable Polymers

✍ Scribed by Wei-Bor Tsai; Min-Cheng Wang


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
167 KB
Volume
5
Category
Article
ISSN
1616-5187

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✦ Synopsis


Abstract

Summary: Cell adhesion to a scaffold is a prerequisite for tissue engineering. Many studies have been focused on enhancing cell adhesion to synthetic materials that are used for scaffold fabrication. In this study, we applied an avidin‐biotin binding system to enhance chondrocyte adhesion to biodegradable polymers. Biotin molecules were conjugated to the cell membrane of chondrocytes, and mediated cell adhesion to avidin‐coated surfaces. We demonstrated that immobilization of biotin molecules to chondrocyte surfaces enhanced cell adhesion to avidin‐coated biodegradable polymers such as poly(L‐lactic acid), poly(D,L‐lactic acid), and polycaprolactone, compared to the adhesion of normal chondrocytes to the same type of biodegradable polymer. The biotinylated chondrocytes still maintained their proliferation ability. This study showed the promise of applying the avidin‐biotin system in cartilage tissue engineering.

The adhesion of B‐chondrocytes to avidin‐adsorbed surfaces (PDLLA) in serum‐free medium (♦) and that of normal chondrocytes to untreated surfaces in the serum‐containing media (▪) (control: adhesion of normal chondrocytes to untreated TCPS in the serum‐containing medium (▴)).

magnified imageThe adhesion of B‐chondrocytes to avidin‐adsorbed surfaces (PDLLA) in serum‐free medium (♦) and that of normal chondrocytes to untreated surfaces in the serum‐containing media (▪) (control: adhesion of normal chondrocytes to untreated TCPS in the serum‐containing medium (▴)).


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## Abstract Cell adhesion to a scaffold is a prerequisite for tissue engineering. Many studies have been focused on enhancing cell adhesion to synthetic materials that are used for scaffold fabrication. Previously, we showed that immobilization of biotin molecules to chondrocyte surfaces enhanced c