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3D in-vitro cultures of human bone marrow and Wharton’s jelly derived mesenchymal stromal cells show high chondrogenic potential

In this study, chondrogenic potentials of 3D high-density cultures of Bone Marrow (BM) and Wharton’s Jelly (WJ)-derived mesenchymal stromal cells (MSCs) was investigated by chondrogenesis- and cytokine-related gene expression over a 16-day culture period supplemented with human transforming growth f...

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Autores principales: Lamparelli, Erwin Pavel, Ciardulli, Maria Camilla, Giudice, Valentina, Scala, Pasqualina, Vitolo, Rosa, Dale, Tina Patricia, Selleri, Carmine, Forsyth, Nicholas Robert, Maffulli, Nicola, Della Porta, Giovanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549977/
https://www.ncbi.nlm.nih.gov/pubmed/36225603
http://dx.doi.org/10.3389/fbioe.2022.986310
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author Lamparelli, Erwin Pavel
Ciardulli, Maria Camilla
Giudice, Valentina
Scala, Pasqualina
Vitolo, Rosa
Dale, Tina Patricia
Selleri, Carmine
Forsyth, Nicholas Robert
Maffulli, Nicola
Della Porta, Giovanna
author_facet Lamparelli, Erwin Pavel
Ciardulli, Maria Camilla
Giudice, Valentina
Scala, Pasqualina
Vitolo, Rosa
Dale, Tina Patricia
Selleri, Carmine
Forsyth, Nicholas Robert
Maffulli, Nicola
Della Porta, Giovanna
author_sort Lamparelli, Erwin Pavel
collection PubMed
description In this study, chondrogenic potentials of 3D high-density cultures of Bone Marrow (BM) and Wharton’s Jelly (WJ)-derived mesenchymal stromal cells (MSCs) was investigated by chondrogenesis- and cytokine-related gene expression over a 16-day culture period supplemented with human transforming growth factor (hTGF)-β1 at 10 ng/ml. In BM-MSC 3D models, a marked upregulation of chondrogenesis-related genes, such as SOX9, COL2A1, and ACAN (all p < 0.05) and formation of spherical pellets with structured type II collagen fibers were observed. Similarly, WJ-based high-density culture appeared higher in size and more regular in shape, with a significant overexpression of COL2A1 and ACAN (all p < 0.05) at day 16. Moreover, a similar upregulation trend was documented for IL-6 and IL-10 expression in both BM and WJ 3D systems. In conclusion, MSC-based high-density cultures can be considered a promising in vitro model of cartilage regeneration and tissue engineering. Moreover, our data support the use of WJ-MSCs as a valid alternative for chondrogenic commitment of stem cells in regenerative medicine.
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spelling pubmed-95499772022-10-11 3D in-vitro cultures of human bone marrow and Wharton’s jelly derived mesenchymal stromal cells show high chondrogenic potential Lamparelli, Erwin Pavel Ciardulli, Maria Camilla Giudice, Valentina Scala, Pasqualina Vitolo, Rosa Dale, Tina Patricia Selleri, Carmine Forsyth, Nicholas Robert Maffulli, Nicola Della Porta, Giovanna Front Bioeng Biotechnol Bioengineering and Biotechnology In this study, chondrogenic potentials of 3D high-density cultures of Bone Marrow (BM) and Wharton’s Jelly (WJ)-derived mesenchymal stromal cells (MSCs) was investigated by chondrogenesis- and cytokine-related gene expression over a 16-day culture period supplemented with human transforming growth factor (hTGF)-β1 at 10 ng/ml. In BM-MSC 3D models, a marked upregulation of chondrogenesis-related genes, such as SOX9, COL2A1, and ACAN (all p < 0.05) and formation of spherical pellets with structured type II collagen fibers were observed. Similarly, WJ-based high-density culture appeared higher in size and more regular in shape, with a significant overexpression of COL2A1 and ACAN (all p < 0.05) at day 16. Moreover, a similar upregulation trend was documented for IL-6 and IL-10 expression in both BM and WJ 3D systems. In conclusion, MSC-based high-density cultures can be considered a promising in vitro model of cartilage regeneration and tissue engineering. Moreover, our data support the use of WJ-MSCs as a valid alternative for chondrogenic commitment of stem cells in regenerative medicine. Frontiers Media S.A. 2022-09-26 /pmc/articles/PMC9549977/ /pubmed/36225603 http://dx.doi.org/10.3389/fbioe.2022.986310 Text en Copyright © 2022 Lamparelli, Ciardulli, Giudice, Scala, Vitolo, Dale, Selleri, Forsyth, Maffulli and Della Porta. https://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) and the copyright owner(s) 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 Bioengineering and Biotechnology
Lamparelli, Erwin Pavel
Ciardulli, Maria Camilla
Giudice, Valentina
Scala, Pasqualina
Vitolo, Rosa
Dale, Tina Patricia
Selleri, Carmine
Forsyth, Nicholas Robert
Maffulli, Nicola
Della Porta, Giovanna
3D in-vitro cultures of human bone marrow and Wharton’s jelly derived mesenchymal stromal cells show high chondrogenic potential
title 3D in-vitro cultures of human bone marrow and Wharton’s jelly derived mesenchymal stromal cells show high chondrogenic potential
title_full 3D in-vitro cultures of human bone marrow and Wharton’s jelly derived mesenchymal stromal cells show high chondrogenic potential
title_fullStr 3D in-vitro cultures of human bone marrow and Wharton’s jelly derived mesenchymal stromal cells show high chondrogenic potential
title_full_unstemmed 3D in-vitro cultures of human bone marrow and Wharton’s jelly derived mesenchymal stromal cells show high chondrogenic potential
title_short 3D in-vitro cultures of human bone marrow and Wharton’s jelly derived mesenchymal stromal cells show high chondrogenic potential
title_sort 3d in-vitro cultures of human bone marrow and wharton’s jelly derived mesenchymal stromal cells show high chondrogenic potential
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549977/
https://www.ncbi.nlm.nih.gov/pubmed/36225603
http://dx.doi.org/10.3389/fbioe.2022.986310
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