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Enhancing chondrogenic potential via mesenchymal stem cell sheet multilayering

Advanced tissue engineering approaches for direct articular cartilage replacement in vivo employ mesenchymal stem cell (MSC) sources, exploiting innate chondrogenic potential to fabricate hyaline-like constructs in vitro within three-dimensional (3D) culture conditions. Cell sheet technology represe...

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Autores principales: Thorp, Hallie, Kim, Kyungsook, Bou-Ghannam, Sophia, Kondo, Makoto, Maak, Travis, Grainger, David W., Okano, Teruo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645782/
https://www.ncbi.nlm.nih.gov/pubmed/34926734
http://dx.doi.org/10.1016/j.reth.2021.11.004
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author Thorp, Hallie
Kim, Kyungsook
Bou-Ghannam, Sophia
Kondo, Makoto
Maak, Travis
Grainger, David W.
Okano, Teruo
author_facet Thorp, Hallie
Kim, Kyungsook
Bou-Ghannam, Sophia
Kondo, Makoto
Maak, Travis
Grainger, David W.
Okano, Teruo
author_sort Thorp, Hallie
collection PubMed
description Advanced tissue engineering approaches for direct articular cartilage replacement in vivo employ mesenchymal stem cell (MSC) sources, exploiting innate chondrogenic potential to fabricate hyaline-like constructs in vitro within three-dimensional (3D) culture conditions. Cell sheet technology represents one such advanced 3D scaffold-free cell culture platform, and previous work has shown that 3D MSC sheets are capable of in vitro hyaline-like chondrogenic differentiation. The present study aims to build upon this understanding and elucidate the effects of an established cell sheet manipulation technique, cell sheet multilayering, on fabrication of MSC-derived hyaline-like cartilage 3D layered constructs in vitro. To achieve this goal, multilayered MSC sheets are prepared and assessed for structural and biochemical transitions throughout chondrogenesis. Results support MSC multilayering as a means of increasing construct thickness and 3D cellular interactions related to in vitro chondrogenesis, including N-cadherin, connexin 43, and integrin β-1. Data indicate that increasing construct thickness from 14 μm (1-layer construct) to 25 μm (2-layer construct) increases these cellular interactions and subsequent in vitro MSC chondrogenesis. However, a clear initial thickness threshold (33 μm - 3-layer construct) is evident that decreases the rate and extent of in vitro chondrogenesis, specifically chondrogenic gene expressions (Sox9, aggrecan, type II collagen) and sulfated proteoglycan accumulation in deposited extracellular matrix (ECM). Together, these data support the utility of cell sheet multilayering as a platform for tailoring construct thickness and subsequent MSC chondrogenesis for future articular cartilage regeneration applications.
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spelling pubmed-86457822021-12-17 Enhancing chondrogenic potential via mesenchymal stem cell sheet multilayering Thorp, Hallie Kim, Kyungsook Bou-Ghannam, Sophia Kondo, Makoto Maak, Travis Grainger, David W. Okano, Teruo Regen Ther Original Article Advanced tissue engineering approaches for direct articular cartilage replacement in vivo employ mesenchymal stem cell (MSC) sources, exploiting innate chondrogenic potential to fabricate hyaline-like constructs in vitro within three-dimensional (3D) culture conditions. Cell sheet technology represents one such advanced 3D scaffold-free cell culture platform, and previous work has shown that 3D MSC sheets are capable of in vitro hyaline-like chondrogenic differentiation. The present study aims to build upon this understanding and elucidate the effects of an established cell sheet manipulation technique, cell sheet multilayering, on fabrication of MSC-derived hyaline-like cartilage 3D layered constructs in vitro. To achieve this goal, multilayered MSC sheets are prepared and assessed for structural and biochemical transitions throughout chondrogenesis. Results support MSC multilayering as a means of increasing construct thickness and 3D cellular interactions related to in vitro chondrogenesis, including N-cadherin, connexin 43, and integrin β-1. Data indicate that increasing construct thickness from 14 μm (1-layer construct) to 25 μm (2-layer construct) increases these cellular interactions and subsequent in vitro MSC chondrogenesis. However, a clear initial thickness threshold (33 μm - 3-layer construct) is evident that decreases the rate and extent of in vitro chondrogenesis, specifically chondrogenic gene expressions (Sox9, aggrecan, type II collagen) and sulfated proteoglycan accumulation in deposited extracellular matrix (ECM). Together, these data support the utility of cell sheet multilayering as a platform for tailoring construct thickness and subsequent MSC chondrogenesis for future articular cartilage regeneration applications. Japanese Society for Regenerative Medicine 2021-12-02 /pmc/articles/PMC8645782/ /pubmed/34926734 http://dx.doi.org/10.1016/j.reth.2021.11.004 Text en © 2021 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Thorp, Hallie
Kim, Kyungsook
Bou-Ghannam, Sophia
Kondo, Makoto
Maak, Travis
Grainger, David W.
Okano, Teruo
Enhancing chondrogenic potential via mesenchymal stem cell sheet multilayering
title Enhancing chondrogenic potential via mesenchymal stem cell sheet multilayering
title_full Enhancing chondrogenic potential via mesenchymal stem cell sheet multilayering
title_fullStr Enhancing chondrogenic potential via mesenchymal stem cell sheet multilayering
title_full_unstemmed Enhancing chondrogenic potential via mesenchymal stem cell sheet multilayering
title_short Enhancing chondrogenic potential via mesenchymal stem cell sheet multilayering
title_sort enhancing chondrogenic potential via mesenchymal stem cell sheet multilayering
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645782/
https://www.ncbi.nlm.nih.gov/pubmed/34926734
http://dx.doi.org/10.1016/j.reth.2021.11.004
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