z-logo
open-access-imgOpen Access
Optimization of a Chondrogenic Medium Through the Use of Factorial Design of Experiments
Author(s) -
Lars Enochson,
Mats Brittberg,
Anders Lindahl
Publication year - 2012
Publication title -
bioresearch open access
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.457
H-Index - 26
eISSN - 2164-7860
pISSN - 2164-7844
DOI - 10.1089/biores.2012.0277
Subject(s) - chondrocyte , chondrogenesis , chemistry , glycosaminoglycan , factorial experiment , microbiology and biotechnology , in vitro , chemically defined medium , cartilage , biomedical engineering , biochemistry , biology , anatomy , computer science , medicine , machine learning
The standard culture system for in vitro cartilage research is based on cells in a three-dimensional micromass culture and a defined medium containing the chondrogenic key growth factor, transforming growth factor (TGF)-β1. The aim of this study was to optimize the medium for chondrocyte micromass culture. Human chondrocytes were cultured in different media formulations, designed with a factorial design of experiments (DoE) approach and based on the standard medium for redifferentiation. The significant factors for the redifferentiation of the chondrocytes were determined and optimized in a two-step process through the use of response surface methodology. TGF-β1, dexamethasone, and glucose were significant factors for differentiating the chondrocytes. Compared to the standard medium, TGF-β1 was increased 30%, dexamethasone reduced 50%, and glucose increased 22%. The potency of the optimized medium was validated in a comparative study against the standard medium. The optimized medium resulted in micromass cultures with increased expression of genes important for the articular chondrocyte phenotype and in cultures with increased glycosaminoglycan/DNA content. Optimizing the standard medium with the efficient DoE method, a new medium that gave better redifferentiation for articular chondrocytes was determined.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here