Comparison of Phenotypic Characterization between "Alginate Bead" and "Pellet Culture Systems as Chondrogenic Differentiation Models for Human Mesenchymal Stem Cells

Chondrogenesis involves the recruitment of mesenchymal cells to differentiate into chondroblasts, and also the cells must synthesize a cartilage-specific extracellular matrix. There were two representative culture systems that promoted the chondrogenic differentiation of human mesenchymal stem cells...

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Published inYonsei medical journal pp. 891 - 900
Main Authors 양익환, 김수향, 김윤희, 선현진, 김성재, 이진우
Format Journal Article
LanguageKorean
Published 연세대학교의과대학 01.10.2004
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ISSN0513-5796
1976-2437

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Summary:Chondrogenesis involves the recruitment of mesenchymal cells to differentiate into chondroblasts, and also the cells must synthesize a cartilage-specific extracellular matrix. There were two representative culture systems that promoted the chondrogenic differentiation of human mesenchymal stem cells. These systems were adaptations of the “pellet” culture system, which was originally described as a method for preventing the phenotypic modulation of chondrocytes, and the “alginate bead” culture system, which was used to maintain encapsulated cells at their differentiated phenotype over time, and also it was used to maintain the cells' proteoglycan synthesis at a rate similar to that of primary chondrocytes. We performed test on the differences of phenotypic characterization with the two methods of differentiating human mesenchymal stem cells into chondrocytes. The typical gene for articular cartilage, collagen type II, was more strongly expressed in the “alginate bead” system than in the “pellet” culture system, in addition, specific gene for hypertrophic cartilage, collagen type X, was more rapidly expressed in the “pellet” system than in “alginate bead” culture system. Therefore, the “alginate bead” culture system is a more phenotypical, practical and appropriate system to differentiate human mesenchymal stem cells into articular chondrocytes than the “pellet” culture system. KCI Citation Count: 40
Bibliography:G704-000409.2004.45.5.010
http://kmbase.medric.or.kr/Main.aspx?d=KMBASE&m=VIEW&i=0311120040450050891
ISSN:0513-5796
1976-2437