Literature DB >> 23197468

Development of large engineered cartilage constructs from a small population of cells.

Jillian M Brenner1, Manuela Kunz, Man Yat Tse, Andrew Winterborn, Davide D Bardana, Stephen C Pang, Stephen D Waldman.   

Abstract

Confronted with articular cartilage's limited capacity for self-repair, joint resurfacing techniques offer an attractive treatment for damaged or diseased tissue. Although tissue engineered cartilage constructs can be created, a substantial number of cells are required to generate sufficient quantities of tissue for the repair of large defects. As routine cell expansion methods tend to elicit negative effects on chondrocyte function, we have developed an approach to generate phenotypically stable, large-sized engineered constructs (≥3 cm(2) ) directly from a small amount of donor tissue or cells (as little as 20,000 cells to generate a 3 cm(2) tissue construct). Using rabbit donor tissue, the bioreactor-cultivated constructs were hyaline-like in appearance and possessed a biochemical composition similar to native articular cartilage. Longer bioreactor cultivation times resulted in increased matrix deposition and improved mechanical properties determined over a 4 week period. Additionally, as the anatomy of the joint will need to be taken in account to effectively resurface large affected areas, we have also explored the possibility of generating constructs matched to the shape and surface geometry of a defect site through the use of rapid-prototyped defect tissue culture molds. Similar hyaline-like tissue constructs were developed that also possessed a high degree of shape correlation to the original defect mold. Future studies will be aimed at determining the effectiveness of this approach to the repair of cartilage defects in an animal model and the creation of large-sized osteochondral constructs.
Copyright © 2012 American Institute of Chemical Engineers (AIChE).

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Year:  2013        PMID: 23197468     DOI: 10.1002/btpr.1670

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


  6 in total

1.  Development of scaffold-free elastic cartilaginous constructs with structural similarities to auricular cartilage.

Authors:  Renata Giardini-Rosa; Paulo P Joazeiro; Kathryn Thomas; Kristina Collavino; Joanna Weber; Stephen D Waldman
Journal:  Tissue Eng Part A       Date:  2014-01-21       Impact factor: 3.845

2.  Scaffold-free cartilage subjected to frictional shear stress demonstrates damage by cracking and surface peeling.

Authors:  G Adam Whitney; Karthik Jayaraman; James E Dennis; Joseph M Mansour
Journal:  J Tissue Eng Regen Med       Date:  2014-06-26       Impact factor: 3.963

3.  Extracellular matrix domain formation as an indicator of chondrocyte dedifferentiation and hypertrophy.

Authors:  Ling Wu; Stephanie Gonzalez; Saumya Shah; Levon Kyupelyan; Frank A Petrigliano; David R McAllister; John S Adams; Marcel Karperien; Tai-Lan Tuan; Paul D Benya; Denis Evseenko
Journal:  Tissue Eng Part C Methods       Date:  2013-07-23       Impact factor: 3.056

4.  Cell Cycle Synchronization of Primary Articular Chondrocytes Enhances Chondrogenesis.

Authors:  Omar D Subedar; Loraine L Y Chiu; Stephen D Waldman
Journal:  Cartilage       Date:  2019-04-11       Impact factor: 4.634

5.  Growth factor stimulation improves the structure and properties of scaffold-free engineered auricular cartilage constructs.

Authors:  Renata G Rosa; Paulo P Joazeiro; Juares Bianco; Manuela Kunz; Joanna F Weber; Stephen D Waldman
Journal:  PLoS One       Date:  2014-08-15       Impact factor: 3.240

6.  Development of a Method for Scaffold-Free Elastic Cartilage Creation.

Authors:  Masahiro Enomura; Soichiro Murata; Yuri Terado; Maiko Tanaka; Shinji Kobayashi; Takayoshi Oba; Shintaro Kagimoto; Yuichiro Yabuki; Kenichi Morita; Toshimasa Uemura; Jiro Maegawa; Hideki Taniguchi
Journal:  Int J Mol Sci       Date:  2020-11-11       Impact factor: 5.923

  6 in total

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