Cargando…

Investigation of multiphasic 3D‐bioplotted scaffolds for site‐specific chondrogenic and osteogenic differentiation of human adipose‐derived stem cells for osteochondral tissue engineering applications

Osteoarthritis is a degenerative joint disease that limits mobility of the affected joint due to the degradation of articular cartilage and subchondral bone. The limited regenerative capacity of cartilage presents significant challenges when attempting to repair or reverse the effects of cartilage d...

Descripción completa

Detalles Bibliográficos
Autores principales: Mellor, Liliana F., Nordberg, Rachel C., Huebner, Pedro, Mohiti‐Asli, Mahsa, Taylor, Michael A., Efird, William, Oxford, Julia T., Spang, Jeffrey T., Shirwaiker, Rohan A., Loboa, Elizabeth G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217039/
https://www.ncbi.nlm.nih.gov/pubmed/31880408
http://dx.doi.org/10.1002/jbm.b.34542
_version_ 1783532535779688448
author Mellor, Liliana F.
Nordberg, Rachel C.
Huebner, Pedro
Mohiti‐Asli, Mahsa
Taylor, Michael A.
Efird, William
Oxford, Julia T.
Spang, Jeffrey T.
Shirwaiker, Rohan A.
Loboa, Elizabeth G.
author_facet Mellor, Liliana F.
Nordberg, Rachel C.
Huebner, Pedro
Mohiti‐Asli, Mahsa
Taylor, Michael A.
Efird, William
Oxford, Julia T.
Spang, Jeffrey T.
Shirwaiker, Rohan A.
Loboa, Elizabeth G.
author_sort Mellor, Liliana F.
collection PubMed
description Osteoarthritis is a degenerative joint disease that limits mobility of the affected joint due to the degradation of articular cartilage and subchondral bone. The limited regenerative capacity of cartilage presents significant challenges when attempting to repair or reverse the effects of cartilage degradation. Tissue engineered medical products are a promising alternative to treat osteochondral degeneration due to their potential to integrate into the patient's existing tissue. The goal of this study was to create a scaffold that would induce site‐specific osteogenic and chondrogenic differentiation of human adipose‐derived stem cells (hASC) to generate a full osteochondral implant. Scaffolds were fabricated using 3D‐bioplotting of biodegradable polycraprolactone (PCL) with either β‐tricalcium phosphate (TCP) or decellularized bovine cartilage extracellular matrix (dECM) to drive site‐specific hASC osteogenesis and chondrogenesis, respectively. PCL‐dECM scaffolds demonstrated elevated matrix deposition and organization in scaffolds seeded with hASC as well as a reduction in collagen I gene expression. 3D‐bioplotted PCL scaffolds with 20% TCP demonstrated elevated calcium deposition, endogenous alkaline phosphatase activity, and osteopontin gene expression. Osteochondral scaffolds comprised of hASC‐seeded 3D‐bioplotted PCL‐TCP, electrospun PCL, and 3D‐bioplotted PCL‐dECM phases were evaluated and demonstrated site‐specific osteochondral tissue characteristics. This technique holds great promise as cartilage morbidity is minimized since autologous cartilage harvest is not required, tissue rejection is minimized via use of an abundant and accessible source of autologous stem cells, and biofabrication techniques allow for a precise, customizable methodology to rapidly produce the scaffold.
format Online
Article
Text
id pubmed-7217039
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-72170392020-05-13 Investigation of multiphasic 3D‐bioplotted scaffolds for site‐specific chondrogenic and osteogenic differentiation of human adipose‐derived stem cells for osteochondral tissue engineering applications Mellor, Liliana F. Nordberg, Rachel C. Huebner, Pedro Mohiti‐Asli, Mahsa Taylor, Michael A. Efird, William Oxford, Julia T. Spang, Jeffrey T. Shirwaiker, Rohan A. Loboa, Elizabeth G. J Biomed Mater Res B Appl Biomater Original Research Reports Osteoarthritis is a degenerative joint disease that limits mobility of the affected joint due to the degradation of articular cartilage and subchondral bone. The limited regenerative capacity of cartilage presents significant challenges when attempting to repair or reverse the effects of cartilage degradation. Tissue engineered medical products are a promising alternative to treat osteochondral degeneration due to their potential to integrate into the patient's existing tissue. The goal of this study was to create a scaffold that would induce site‐specific osteogenic and chondrogenic differentiation of human adipose‐derived stem cells (hASC) to generate a full osteochondral implant. Scaffolds were fabricated using 3D‐bioplotting of biodegradable polycraprolactone (PCL) with either β‐tricalcium phosphate (TCP) or decellularized bovine cartilage extracellular matrix (dECM) to drive site‐specific hASC osteogenesis and chondrogenesis, respectively. PCL‐dECM scaffolds demonstrated elevated matrix deposition and organization in scaffolds seeded with hASC as well as a reduction in collagen I gene expression. 3D‐bioplotted PCL scaffolds with 20% TCP demonstrated elevated calcium deposition, endogenous alkaline phosphatase activity, and osteopontin gene expression. Osteochondral scaffolds comprised of hASC‐seeded 3D‐bioplotted PCL‐TCP, electrospun PCL, and 3D‐bioplotted PCL‐dECM phases were evaluated and demonstrated site‐specific osteochondral tissue characteristics. This technique holds great promise as cartilage morbidity is minimized since autologous cartilage harvest is not required, tissue rejection is minimized via use of an abundant and accessible source of autologous stem cells, and biofabrication techniques allow for a precise, customizable methodology to rapidly produce the scaffold. John Wiley & Sons, Inc. 2019-12-27 2020-07 /pmc/articles/PMC7217039/ /pubmed/31880408 http://dx.doi.org/10.1002/jbm.b.34542 Text en © 2020 The Authors. Journal of Biomedical Materials Research Part B: Applied Biomaterials published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Reports
Mellor, Liliana F.
Nordberg, Rachel C.
Huebner, Pedro
Mohiti‐Asli, Mahsa
Taylor, Michael A.
Efird, William
Oxford, Julia T.
Spang, Jeffrey T.
Shirwaiker, Rohan A.
Loboa, Elizabeth G.
Investigation of multiphasic 3D‐bioplotted scaffolds for site‐specific chondrogenic and osteogenic differentiation of human adipose‐derived stem cells for osteochondral tissue engineering applications
title Investigation of multiphasic 3D‐bioplotted scaffolds for site‐specific chondrogenic and osteogenic differentiation of human adipose‐derived stem cells for osteochondral tissue engineering applications
title_full Investigation of multiphasic 3D‐bioplotted scaffolds for site‐specific chondrogenic and osteogenic differentiation of human adipose‐derived stem cells for osteochondral tissue engineering applications
title_fullStr Investigation of multiphasic 3D‐bioplotted scaffolds for site‐specific chondrogenic and osteogenic differentiation of human adipose‐derived stem cells for osteochondral tissue engineering applications
title_full_unstemmed Investigation of multiphasic 3D‐bioplotted scaffolds for site‐specific chondrogenic and osteogenic differentiation of human adipose‐derived stem cells for osteochondral tissue engineering applications
title_short Investigation of multiphasic 3D‐bioplotted scaffolds for site‐specific chondrogenic and osteogenic differentiation of human adipose‐derived stem cells for osteochondral tissue engineering applications
title_sort investigation of multiphasic 3d‐bioplotted scaffolds for site‐specific chondrogenic and osteogenic differentiation of human adipose‐derived stem cells for osteochondral tissue engineering applications
topic Original Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217039/
https://www.ncbi.nlm.nih.gov/pubmed/31880408
http://dx.doi.org/10.1002/jbm.b.34542
work_keys_str_mv AT mellorlilianaf investigationofmultiphasic3dbioplottedscaffoldsforsitespecificchondrogenicandosteogenicdifferentiationofhumanadiposederivedstemcellsforosteochondraltissueengineeringapplications
AT nordbergrachelc investigationofmultiphasic3dbioplottedscaffoldsforsitespecificchondrogenicandosteogenicdifferentiationofhumanadiposederivedstemcellsforosteochondraltissueengineeringapplications
AT huebnerpedro investigationofmultiphasic3dbioplottedscaffoldsforsitespecificchondrogenicandosteogenicdifferentiationofhumanadiposederivedstemcellsforosteochondraltissueengineeringapplications
AT mohitiaslimahsa investigationofmultiphasic3dbioplottedscaffoldsforsitespecificchondrogenicandosteogenicdifferentiationofhumanadiposederivedstemcellsforosteochondraltissueengineeringapplications
AT taylormichaela investigationofmultiphasic3dbioplottedscaffoldsforsitespecificchondrogenicandosteogenicdifferentiationofhumanadiposederivedstemcellsforosteochondraltissueengineeringapplications
AT efirdwilliam investigationofmultiphasic3dbioplottedscaffoldsforsitespecificchondrogenicandosteogenicdifferentiationofhumanadiposederivedstemcellsforosteochondraltissueengineeringapplications
AT oxfordjuliat investigationofmultiphasic3dbioplottedscaffoldsforsitespecificchondrogenicandosteogenicdifferentiationofhumanadiposederivedstemcellsforosteochondraltissueengineeringapplications
AT spangjeffreyt investigationofmultiphasic3dbioplottedscaffoldsforsitespecificchondrogenicandosteogenicdifferentiationofhumanadiposederivedstemcellsforosteochondraltissueengineeringapplications
AT shirwaikerrohana investigationofmultiphasic3dbioplottedscaffoldsforsitespecificchondrogenicandosteogenicdifferentiationofhumanadiposederivedstemcellsforosteochondraltissueengineeringapplications
AT loboaelizabethg investigationofmultiphasic3dbioplottedscaffoldsforsitespecificchondrogenicandosteogenicdifferentiationofhumanadiposederivedstemcellsforosteochondraltissueengineeringapplications