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Chondrocyte De-Differentiation: Biophysical Cues to Nuclear Alterations

Autologous chondrocyte implantation (ACI) is a cell therapy to repair cartilage defects. In ACI a biopsy is taken from a non-load bearing area of the knee and expanded in-vitro. The expansion process provides the benefit of generating a large number of cells required for implantation; however, durin...

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Autores principales: Al-Maslamani, Noor A., Oldershaw, Rachel, Tew, Simon, Curran, Jude, D’Hooghe, Pieter, Yamamoto, Kazuhiro, Horn, Henning F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9777101/
https://www.ncbi.nlm.nih.gov/pubmed/36552775
http://dx.doi.org/10.3390/cells11244011
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author Al-Maslamani, Noor A.
Oldershaw, Rachel
Tew, Simon
Curran, Jude
D’Hooghe, Pieter
Yamamoto, Kazuhiro
Horn, Henning F.
author_facet Al-Maslamani, Noor A.
Oldershaw, Rachel
Tew, Simon
Curran, Jude
D’Hooghe, Pieter
Yamamoto, Kazuhiro
Horn, Henning F.
author_sort Al-Maslamani, Noor A.
collection PubMed
description Autologous chondrocyte implantation (ACI) is a cell therapy to repair cartilage defects. In ACI a biopsy is taken from a non-load bearing area of the knee and expanded in-vitro. The expansion process provides the benefit of generating a large number of cells required for implantation; however, during the expansion these cells de-differentiate and lose their chondrocyte phenotype. In this review we focus on examining the de-differentiation phenotype from a mechanobiology and biophysical perspective, highlighting some of the nuclear mechanics and chromatin changes in chondrocytes seen during the expansion process and how this relates to the gene expression profile. We propose that manipulating chondrocyte nuclear architecture and chromatin organization will highlight mechanisms that will help to preserve the chondrocyte phenotype.
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spelling pubmed-97771012022-12-23 Chondrocyte De-Differentiation: Biophysical Cues to Nuclear Alterations Al-Maslamani, Noor A. Oldershaw, Rachel Tew, Simon Curran, Jude D’Hooghe, Pieter Yamamoto, Kazuhiro Horn, Henning F. Cells Review Autologous chondrocyte implantation (ACI) is a cell therapy to repair cartilage defects. In ACI a biopsy is taken from a non-load bearing area of the knee and expanded in-vitro. The expansion process provides the benefit of generating a large number of cells required for implantation; however, during the expansion these cells de-differentiate and lose their chondrocyte phenotype. In this review we focus on examining the de-differentiation phenotype from a mechanobiology and biophysical perspective, highlighting some of the nuclear mechanics and chromatin changes in chondrocytes seen during the expansion process and how this relates to the gene expression profile. We propose that manipulating chondrocyte nuclear architecture and chromatin organization will highlight mechanisms that will help to preserve the chondrocyte phenotype. MDPI 2022-12-12 /pmc/articles/PMC9777101/ /pubmed/36552775 http://dx.doi.org/10.3390/cells11244011 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Al-Maslamani, Noor A.
Oldershaw, Rachel
Tew, Simon
Curran, Jude
D’Hooghe, Pieter
Yamamoto, Kazuhiro
Horn, Henning F.
Chondrocyte De-Differentiation: Biophysical Cues to Nuclear Alterations
title Chondrocyte De-Differentiation: Biophysical Cues to Nuclear Alterations
title_full Chondrocyte De-Differentiation: Biophysical Cues to Nuclear Alterations
title_fullStr Chondrocyte De-Differentiation: Biophysical Cues to Nuclear Alterations
title_full_unstemmed Chondrocyte De-Differentiation: Biophysical Cues to Nuclear Alterations
title_short Chondrocyte De-Differentiation: Biophysical Cues to Nuclear Alterations
title_sort chondrocyte de-differentiation: biophysical cues to nuclear alterations
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9777101/
https://www.ncbi.nlm.nih.gov/pubmed/36552775
http://dx.doi.org/10.3390/cells11244011
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