Literature DB >> 19572391

Pellet culture elicits superior chondrogenic redifferentiation than alginate-based systems.

Peter Bernstein1, Meng Dong, Denis Corbeil, Michael Gelinsky, Klaus-Peter Günther, Stefan Fickert.   

Abstract

Although pellet culture and encapsulation of chondrocytes into gel-like biomaterials have lead to major advances in cartilage tissue engineering, a quantitative comparative characterization of cellular differentiation behavior during those cultivation procedures has not yet been performed. Our study therefore aimed at answering the following question: is the redifferentiation pathway of chondrocytes altered by slight changes in the type of alginate biomaterial (pure alginate, alginate-fibrin, alginate-chitosan) and how do the cells behave in comparison to biomaterial-free (pellet) three-dimensional culturing? Monolayer-expanded chondrocytes from healthy adult porcine knee joints were cultivated in alginate, alginate-chitosan, alginate-fibrin beads and as pellets up to 4 weeks. Quantitative PCR and Immunohistology were used to assess chondrogenic markers. Alginate-fibrin-encapsulated chondrocytes behaved almost like monolayer chondrocytes. Alginate- and alginate-chitosan encapsulation lead to a low chondrogenic marker gene expression. Although all 3D-cultured chondrocytes showed a considerable amount of Sox9 expression, only pellet cultivation lead to a sufficient Collagen II expression. This puts the usage of alginate-cultivated cartilage tissue engineering constructs under question. Fibrin addition is not beneficial for chondrogenic differentiation. Sox9 and Collagen II behave differently, depending upon the surrounding 3D-environment. (c) 2009 American Institute of Chemical Engineers AIChE J, 2009.

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Year:  2009        PMID: 19572391     DOI: 10.1002/btpr.186

Source DB:  PubMed          Journal:  Biotechnol Prog        ISSN: 1520-6033


  19 in total

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3.  An Innovative Laboratory Procedure to Expand Chondrocytes with Reduced Dedifferentiation.

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4.  Engineering a fibrocartilage spectrum through modulation of aggregate redifferentiation.

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5.  Characterization of ex vivo-generated bovine and human cartilage by immunohistochemical, biochemical, and magnetic resonance imaging analyses.

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Journal:  Tissue Eng Part A       Date:  2010-07       Impact factor: 3.845

6.  Genetic engineering of juvenile human chondrocytes improves scaffold-free mosaic neocartilage grafts.

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Review 8.  Monitoring cartilage tissue engineering using magnetic resonance spectroscopy, imaging, and elastography.

Authors:  Mrignayani Kotecha; Dieter Klatt; Richard L Magin
Journal:  Tissue Eng Part B Rev       Date:  2013-06-04       Impact factor: 6.389

9.  Tension-compression loading with chemical stimulation results in additive increases to functional properties of anatomic meniscal constructs.

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Journal:  PLoS One       Date:  2011-11-16       Impact factor: 3.240

10.  Platelet-rich plasma releasate differently stimulates cellular commitment toward the chondrogenic lineage according to concentration.

Authors:  Ronaldo Jfc do Amaral; Amos Matsiko; Marcel Rp Tomazette; Wanessa Kr Rocha; Eric Cordeiro-Spinetti; Tanya J Levingstone; Marcos Farina; Fergal J O'Brien; Marcia C El-Cheikh; Alex Balduino
Journal:  J Tissue Eng       Date:  2015-07-07       Impact factor: 7.813

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