Matrix development in self-assembly of articular cartilage.

Articular cartilage is a highly functional tissue which covers the ends of long bones and serves to ensure proper joint movement. A tissue engineering approach that recapitulates the developmental characteristics of articular cartilage can be used to examine the maturation and degeneration of cartil...

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Main Authors: Gidon Ofek, Christopher M Revell, Jerry C Hu, David D Allison, K Jane Grande-Allen, Kyriacos A Athanasiou
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-07-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2464773?pdf=render
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spelling doaj-b2455030ff52437094ff6b2aa440ef072020-11-25T02:13:35ZengPublic Library of Science (PLoS)PLoS ONE1932-62032008-07-0137e279510.1371/journal.pone.0002795Matrix development in self-assembly of articular cartilage.Gidon OfekChristopher M RevellJerry C HuDavid D AllisonK Jane Grande-AllenKyriacos A AthanasiouArticular cartilage is a highly functional tissue which covers the ends of long bones and serves to ensure proper joint movement. A tissue engineering approach that recapitulates the developmental characteristics of articular cartilage can be used to examine the maturation and degeneration of cartilage and produce fully functional neotissue replacements for diseased tissue.This study examined the development of articular cartilage neotissue within a self-assembling process in two phases. In the first phase, articular cartilage constructs were examined at 1, 4, 7, 10, 14, 28, 42, and 56 days immunohistochemically, histologically, and through biochemical analysis for total collagen and glycosaminoglycan (GAG) content. Based on statistical changes in GAG and collagen levels, four time points from the first phase (7, 14, 28, and 56 days) were chosen to carry into the second phase, where the constructs were studied in terms of their mechanical characteristics, relative amounts of collagen types II and VI, and specific GAG types (chondroitin 4-sulfate, chondroitin 6-sulfate, dermatan sulfate, and hyaluronan). Collagen type VI was present in initial abundance and then localized to a pericellular distribution at 4 wks. N-cadherin activity also spiked at early stages of neotissue development, suggesting that self-assembly is mediated through a minimization of free energy. The percentage of collagen type II to total collagen significantly increased over time, while the proportion of collagen type VI to total collagen decreased between 1 and 2 wks. The chondroitin 6- to 4- sulfate ratio decreased steadily during construct maturation. In addition, the compressive properties reached a plateau and tensile characteristics peaked at 4 wks.The indices of cartilage formation examined in this study suggest that tissue maturation in self-assembled articular cartilage mirrors known developmental processes for native tissue. In terms of tissue engineering, it is suggested that exogenous stimulation may be necessary after 4 wks to further augment the functionality of developing constructs.http://europepmc.org/articles/PMC2464773?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Gidon Ofek
Christopher M Revell
Jerry C Hu
David D Allison
K Jane Grande-Allen
Kyriacos A Athanasiou
spellingShingle Gidon Ofek
Christopher M Revell
Jerry C Hu
David D Allison
K Jane Grande-Allen
Kyriacos A Athanasiou
Matrix development in self-assembly of articular cartilage.
PLoS ONE
author_facet Gidon Ofek
Christopher M Revell
Jerry C Hu
David D Allison
K Jane Grande-Allen
Kyriacos A Athanasiou
author_sort Gidon Ofek
title Matrix development in self-assembly of articular cartilage.
title_short Matrix development in self-assembly of articular cartilage.
title_full Matrix development in self-assembly of articular cartilage.
title_fullStr Matrix development in self-assembly of articular cartilage.
title_full_unstemmed Matrix development in self-assembly of articular cartilage.
title_sort matrix development in self-assembly of articular cartilage.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2008-07-01
description Articular cartilage is a highly functional tissue which covers the ends of long bones and serves to ensure proper joint movement. A tissue engineering approach that recapitulates the developmental characteristics of articular cartilage can be used to examine the maturation and degeneration of cartilage and produce fully functional neotissue replacements for diseased tissue.This study examined the development of articular cartilage neotissue within a self-assembling process in two phases. In the first phase, articular cartilage constructs were examined at 1, 4, 7, 10, 14, 28, 42, and 56 days immunohistochemically, histologically, and through biochemical analysis for total collagen and glycosaminoglycan (GAG) content. Based on statistical changes in GAG and collagen levels, four time points from the first phase (7, 14, 28, and 56 days) were chosen to carry into the second phase, where the constructs were studied in terms of their mechanical characteristics, relative amounts of collagen types II and VI, and specific GAG types (chondroitin 4-sulfate, chondroitin 6-sulfate, dermatan sulfate, and hyaluronan). Collagen type VI was present in initial abundance and then localized to a pericellular distribution at 4 wks. N-cadherin activity also spiked at early stages of neotissue development, suggesting that self-assembly is mediated through a minimization of free energy. The percentage of collagen type II to total collagen significantly increased over time, while the proportion of collagen type VI to total collagen decreased between 1 and 2 wks. The chondroitin 6- to 4- sulfate ratio decreased steadily during construct maturation. In addition, the compressive properties reached a plateau and tensile characteristics peaked at 4 wks.The indices of cartilage formation examined in this study suggest that tissue maturation in self-assembled articular cartilage mirrors known developmental processes for native tissue. In terms of tissue engineering, it is suggested that exogenous stimulation may be necessary after 4 wks to further augment the functionality of developing constructs.
url http://europepmc.org/articles/PMC2464773?pdf=render
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