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Cartilage Tissue Engineering by the 3D Bioprinting of iPS Cells in a Nanocellulose/Alginate Bioink

Cartilage lesions can progress into secondary osteoarthritis and cause severe clinical problems in numerous patients. As a prospective treatment of such lesions, human-derived induced pluripotent stem cells (iPSCs) were shown to be 3D bioprinted into cartilage mimics using a nanofibrillated cellulos...

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Autores principales: Nguyen, Duong, Hägg, Daniel A., Forsman, Alma, Ekholm, Josefine, Nimkingratana, Puwapong, Brantsing, Camilla, Kalogeropoulos, Theodoros, Zaunz, Samantha, Concaro, Sebastian, Brittberg, Mats, Lindahl, Anders, Gatenholm, Paul, Enejder, Annika, Simonsson, Stina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428803/
https://www.ncbi.nlm.nih.gov/pubmed/28386058
http://dx.doi.org/10.1038/s41598-017-00690-y
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author Nguyen, Duong
Hägg, Daniel A.
Forsman, Alma
Ekholm, Josefine
Nimkingratana, Puwapong
Brantsing, Camilla
Kalogeropoulos, Theodoros
Zaunz, Samantha
Concaro, Sebastian
Brittberg, Mats
Lindahl, Anders
Gatenholm, Paul
Enejder, Annika
Simonsson, Stina
author_facet Nguyen, Duong
Hägg, Daniel A.
Forsman, Alma
Ekholm, Josefine
Nimkingratana, Puwapong
Brantsing, Camilla
Kalogeropoulos, Theodoros
Zaunz, Samantha
Concaro, Sebastian
Brittberg, Mats
Lindahl, Anders
Gatenholm, Paul
Enejder, Annika
Simonsson, Stina
author_sort Nguyen, Duong
collection PubMed
description Cartilage lesions can progress into secondary osteoarthritis and cause severe clinical problems in numerous patients. As a prospective treatment of such lesions, human-derived induced pluripotent stem cells (iPSCs) were shown to be 3D bioprinted into cartilage mimics using a nanofibrillated cellulose (NFC) composite bioink when co-printed with irradiated human chondrocytes. Two bioinks were investigated: NFC with alginate (NFC/A) or hyaluronic acid (NFC/HA). Low proliferation and phenotypic changes away from pluripotency were seen in the case of NFC/HA. However, in the case of the 3D-bioprinted NFC/A (60/40, dry weight % ratio) constructs, pluripotency was initially maintained, and after five weeks, hyaline-like cartilaginous tissue with collagen type II expression and lacking tumorigenic Oct4 expression was observed in 3D -bioprinted NFC/A (60/40, dry weight % relation) constructs. Moreover, a marked increase in cell number within the cartilaginous tissue was detected by 2-photon fluorescence microscopy, indicating the importance of high cell densities in the pursuit of achieving good survival after printing. We conclude that NFC/A bioink is suitable for bioprinting iPSCs to support cartilage production in co-cultures with irradiated chondrocytes.
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spelling pubmed-54288032017-05-15 Cartilage Tissue Engineering by the 3D Bioprinting of iPS Cells in a Nanocellulose/Alginate Bioink Nguyen, Duong Hägg, Daniel A. Forsman, Alma Ekholm, Josefine Nimkingratana, Puwapong Brantsing, Camilla Kalogeropoulos, Theodoros Zaunz, Samantha Concaro, Sebastian Brittberg, Mats Lindahl, Anders Gatenholm, Paul Enejder, Annika Simonsson, Stina Sci Rep Article Cartilage lesions can progress into secondary osteoarthritis and cause severe clinical problems in numerous patients. As a prospective treatment of such lesions, human-derived induced pluripotent stem cells (iPSCs) were shown to be 3D bioprinted into cartilage mimics using a nanofibrillated cellulose (NFC) composite bioink when co-printed with irradiated human chondrocytes. Two bioinks were investigated: NFC with alginate (NFC/A) or hyaluronic acid (NFC/HA). Low proliferation and phenotypic changes away from pluripotency were seen in the case of NFC/HA. However, in the case of the 3D-bioprinted NFC/A (60/40, dry weight % ratio) constructs, pluripotency was initially maintained, and after five weeks, hyaline-like cartilaginous tissue with collagen type II expression and lacking tumorigenic Oct4 expression was observed in 3D -bioprinted NFC/A (60/40, dry weight % relation) constructs. Moreover, a marked increase in cell number within the cartilaginous tissue was detected by 2-photon fluorescence microscopy, indicating the importance of high cell densities in the pursuit of achieving good survival after printing. We conclude that NFC/A bioink is suitable for bioprinting iPSCs to support cartilage production in co-cultures with irradiated chondrocytes. Nature Publishing Group UK 2017-04-06 /pmc/articles/PMC5428803/ /pubmed/28386058 http://dx.doi.org/10.1038/s41598-017-00690-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Nguyen, Duong
Hägg, Daniel A.
Forsman, Alma
Ekholm, Josefine
Nimkingratana, Puwapong
Brantsing, Camilla
Kalogeropoulos, Theodoros
Zaunz, Samantha
Concaro, Sebastian
Brittberg, Mats
Lindahl, Anders
Gatenholm, Paul
Enejder, Annika
Simonsson, Stina
Cartilage Tissue Engineering by the 3D Bioprinting of iPS Cells in a Nanocellulose/Alginate Bioink
title Cartilage Tissue Engineering by the 3D Bioprinting of iPS Cells in a Nanocellulose/Alginate Bioink
title_full Cartilage Tissue Engineering by the 3D Bioprinting of iPS Cells in a Nanocellulose/Alginate Bioink
title_fullStr Cartilage Tissue Engineering by the 3D Bioprinting of iPS Cells in a Nanocellulose/Alginate Bioink
title_full_unstemmed Cartilage Tissue Engineering by the 3D Bioprinting of iPS Cells in a Nanocellulose/Alginate Bioink
title_short Cartilage Tissue Engineering by the 3D Bioprinting of iPS Cells in a Nanocellulose/Alginate Bioink
title_sort cartilage tissue engineering by the 3d bioprinting of ips cells in a nanocellulose/alginate bioink
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428803/
https://www.ncbi.nlm.nih.gov/pubmed/28386058
http://dx.doi.org/10.1038/s41598-017-00690-y
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