Synergistic Effect of TGF-β1 And BMP-7 on Chondrogenesis and Extracellular Matrix Synthesis: An In Vitro Study

The purpose of the present study seeks to determine the signal timing of BMP-7 and TGF-β1 from a novel chitosan based hydrogel system that may affect chondrocyte proliferation resulting in the presence of a synergism seen conspicuously in consecutive controlled delivery. Four groups of cultured chon...

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Bibliographic Details
Published in:The open orthopaedics journal Vol. 6; no. 1; pp. 406 - 413
Main Authors: Gokce, Alper, Yilmaz, Ibrahim, Bircan, Rifat, Tonbul, Murat, Gokay, Nevzat Selim, Gokce, Cigdem
Format: Journal Article
Language:English
Published: United Arab Emirates Bentham Open 07-09-2012
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Summary:The purpose of the present study seeks to determine the signal timing of BMP-7 and TGF-β1 from a novel chitosan based hydrogel system that may affect chondrocyte proliferation resulting in the presence of a synergism seen conspicuously in consecutive controlled delivery. Four groups of cultured chondrocytes were seeded on a novel designed chitosan based hydrogel. The hydrogel was left empty (control) in one group and loaded with BMP-7, TGF-β1 and their combination in the other groups, respectively. Hydrogel structure was analyzed with scanning electron microscope. The release kinetics of Growth Factors (GFs) was determined with ELISA. Chondrocyte viability and toxicity after being tested with MTS and collagen type II synthesis, were quantified with western blotting. Canonical regression analysis was used for measuring statistical evaluation. Chitosan based hydrogel allowed controlled release of GFs in different time intervals for BMP-7 and TGF-β1. Double peak concentration gradient was found to be present in the group loaded with both GFs. In this group, substantially higher chondrocyte growth and collagen synthesis were also detected. We concluded that, chitosan based hydrogel systems may be adjusted to release GFs consecutively during biodegradation at the layers of surface, which may increase the cell number and enhance collagen type II synthesis.
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ISSN:1874-3250
1874-3250
DOI:10.2174/1874325001206010406