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Chondrogenesis of Human Infrapatellar Fat Pad Stem Cells on Acellular Dermal Matrix

Acellular dermal matrix (ADM) has been in clinical use for decades in numerous surgical applications. The ability for ADM to promote cellular repopulation, revascularisation and tissue regeneration is well documented. Adipose stem cells have the ability to differentiate into mesenchymal tissue types...

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Autores principales: Ye, Ken, Traianedes, Kathy, Choong, Peter F. M., Myers, Damian E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726816/
https://www.ncbi.nlm.nih.gov/pubmed/26858950
http://dx.doi.org/10.3389/fsurg.2016.00003
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author Ye, Ken
Traianedes, Kathy
Choong, Peter F. M.
Myers, Damian E.
author_facet Ye, Ken
Traianedes, Kathy
Choong, Peter F. M.
Myers, Damian E.
author_sort Ye, Ken
collection PubMed
description Acellular dermal matrix (ADM) has been in clinical use for decades in numerous surgical applications. The ability for ADM to promote cellular repopulation, revascularisation and tissue regeneration is well documented. Adipose stem cells have the ability to differentiate into mesenchymal tissue types, including bone and cartilage. The aim of this study was to investigate the potential interaction between ADM and adipose stem cells in vitro using TGFβ3 and BMP6. Human infrapatellar fat pad-derived adipose stem cells (IPFP-ASC) were cultured with ADM derived from rat dermis in chondrogenic (TGFβ3 and BMP6) medium in vitro for 2 and 4 weeks. Histology, qPCR, and immunohistochemistry were performed to assess for markers of chondrogenesis (collagen Type II, SOX9 and proteoglycans). At 4 weeks, cell-scaffold constructs displayed cellular changes consistent with chondrogenesis, with evidence of stratification of cell layers and development of a hyaline-like cartilage layer superficially, which stained positively for collagen Type II and proteoglycans. Significant cell–matrix interaction was seen between the cartilage layer and the ADM itself with seamless integration between each layer. Real time qPCR showed significantly increased COL2A1, SOX9, and ACAN gene expression over 4 weeks when compared to control. COL1A2 gene expression remained unchanged over 4 weeks. We believe that the principles that make ADM versatile and successful for tissue regeneration are applicable to cartilage regeneration. This study demonstrates in vitro the ability for IPFP-ASCs to undergo chondrogenesis, infiltrate, and interact with ADM. These outcomes serve as a platform for in vivo modelling of ADM for cartilage repair.
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spelling pubmed-47268162016-02-08 Chondrogenesis of Human Infrapatellar Fat Pad Stem Cells on Acellular Dermal Matrix Ye, Ken Traianedes, Kathy Choong, Peter F. M. Myers, Damian E. Front Surg Surgery Acellular dermal matrix (ADM) has been in clinical use for decades in numerous surgical applications. The ability for ADM to promote cellular repopulation, revascularisation and tissue regeneration is well documented. Adipose stem cells have the ability to differentiate into mesenchymal tissue types, including bone and cartilage. The aim of this study was to investigate the potential interaction between ADM and adipose stem cells in vitro using TGFβ3 and BMP6. Human infrapatellar fat pad-derived adipose stem cells (IPFP-ASC) were cultured with ADM derived from rat dermis in chondrogenic (TGFβ3 and BMP6) medium in vitro for 2 and 4 weeks. Histology, qPCR, and immunohistochemistry were performed to assess for markers of chondrogenesis (collagen Type II, SOX9 and proteoglycans). At 4 weeks, cell-scaffold constructs displayed cellular changes consistent with chondrogenesis, with evidence of stratification of cell layers and development of a hyaline-like cartilage layer superficially, which stained positively for collagen Type II and proteoglycans. Significant cell–matrix interaction was seen between the cartilage layer and the ADM itself with seamless integration between each layer. Real time qPCR showed significantly increased COL2A1, SOX9, and ACAN gene expression over 4 weeks when compared to control. COL1A2 gene expression remained unchanged over 4 weeks. We believe that the principles that make ADM versatile and successful for tissue regeneration are applicable to cartilage regeneration. This study demonstrates in vitro the ability for IPFP-ASCs to undergo chondrogenesis, infiltrate, and interact with ADM. These outcomes serve as a platform for in vivo modelling of ADM for cartilage repair. Frontiers Media S.A. 2016-01-26 /pmc/articles/PMC4726816/ /pubmed/26858950 http://dx.doi.org/10.3389/fsurg.2016.00003 Text en Copyright © 2016 Ye, Traianedes, Choong and Myers. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Surgery
Ye, Ken
Traianedes, Kathy
Choong, Peter F. M.
Myers, Damian E.
Chondrogenesis of Human Infrapatellar Fat Pad Stem Cells on Acellular Dermal Matrix
title Chondrogenesis of Human Infrapatellar Fat Pad Stem Cells on Acellular Dermal Matrix
title_full Chondrogenesis of Human Infrapatellar Fat Pad Stem Cells on Acellular Dermal Matrix
title_fullStr Chondrogenesis of Human Infrapatellar Fat Pad Stem Cells on Acellular Dermal Matrix
title_full_unstemmed Chondrogenesis of Human Infrapatellar Fat Pad Stem Cells on Acellular Dermal Matrix
title_short Chondrogenesis of Human Infrapatellar Fat Pad Stem Cells on Acellular Dermal Matrix
title_sort chondrogenesis of human infrapatellar fat pad stem cells on acellular dermal matrix
topic Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726816/
https://www.ncbi.nlm.nih.gov/pubmed/26858950
http://dx.doi.org/10.3389/fsurg.2016.00003
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