3D-microtissue derived secretome as a cell-free approach for enhanced mineralization of scaffolds in the chorioallantoic membrane model

Abstract Bone regeneration is a complex process and the clinical translation of tissue engineered constructs (TECs) remains a challenge. The combination of biomaterials and mesenchymal stem cells (MSCs) may enhance the healing process through paracrine effects. Here, we investigated the influence of...

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Autores principales: Lukas Otto, Petra Wolint, Annina Bopp, Anna Woloszyk, Anton S. Becker, Andreas Boss, Roland Böni, Maurizio Calcagni, Pietro Giovanoli, Simon P. Hoerstrup, Maximilian Y. Emmert, Johanna Buschmann
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:13a7a4e40eaf4c73bc17ec0a47a77cc52021-12-02T11:37:18Z3D-microtissue derived secretome as a cell-free approach for enhanced mineralization of scaffolds in the chorioallantoic membrane model10.1038/s41598-021-84123-x2045-2322https://doaj.org/article/13a7a4e40eaf4c73bc17ec0a47a77cc52021-03-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-84123-xhttps://doaj.org/toc/2045-2322Abstract Bone regeneration is a complex process and the clinical translation of tissue engineered constructs (TECs) remains a challenge. The combination of biomaterials and mesenchymal stem cells (MSCs) may enhance the healing process through paracrine effects. Here, we investigated the influence of cell format in combination with a collagen scaffold on key factors in bone healing process, such as mineralization, cell infiltration, vascularization, and ECM production. MSCs as single cells (2D-SCs), assembled into microtissues (3D-MTs) or their corresponding secretomes were combined with a collagen scaffold and incubated on the chicken embryo chorioallantoic membrane (CAM) for 7 days. A comprehensive quantitative analysis was performed on a cellular level by histology and by microcomputed tomography (microCT). In all experimental groups, accumulation of collagen and glycosaminoglycan within the scaffold was observed over time. A pronounced cell infiltration and vascularization from the interface to the surface region of the CAM was detected. The 3D-MT secretome showed a significant mineralization of the biomaterial using microCT compared to all other conditions. Furthermore, it revealed a homogeneous distribution pattern of mineralization deposits in contrast to the cell-based scaffolds, where mineralization was only at the surface. Therefore, the secretome of MSCs assembled into 3D-MTs may represent an interesting therapeutic strategy for a next-generation bone healing concept.Lukas OttoPetra WolintAnnina BoppAnna WoloszykAnton S. BeckerAndreas BossRoland BöniMaurizio CalcagniPietro GiovanoliSimon P. HoerstrupMaximilian Y. EmmertJohanna BuschmannNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Lukas Otto
Petra Wolint
Annina Bopp
Anna Woloszyk
Anton S. Becker
Andreas Boss
Roland Böni
Maurizio Calcagni
Pietro Giovanoli
Simon P. Hoerstrup
Maximilian Y. Emmert
Johanna Buschmann
3D-microtissue derived secretome as a cell-free approach for enhanced mineralization of scaffolds in the chorioallantoic membrane model
description Abstract Bone regeneration is a complex process and the clinical translation of tissue engineered constructs (TECs) remains a challenge. The combination of biomaterials and mesenchymal stem cells (MSCs) may enhance the healing process through paracrine effects. Here, we investigated the influence of cell format in combination with a collagen scaffold on key factors in bone healing process, such as mineralization, cell infiltration, vascularization, and ECM production. MSCs as single cells (2D-SCs), assembled into microtissues (3D-MTs) or their corresponding secretomes were combined with a collagen scaffold and incubated on the chicken embryo chorioallantoic membrane (CAM) for 7 days. A comprehensive quantitative analysis was performed on a cellular level by histology and by microcomputed tomography (microCT). In all experimental groups, accumulation of collagen and glycosaminoglycan within the scaffold was observed over time. A pronounced cell infiltration and vascularization from the interface to the surface region of the CAM was detected. The 3D-MT secretome showed a significant mineralization of the biomaterial using microCT compared to all other conditions. Furthermore, it revealed a homogeneous distribution pattern of mineralization deposits in contrast to the cell-based scaffolds, where mineralization was only at the surface. Therefore, the secretome of MSCs assembled into 3D-MTs may represent an interesting therapeutic strategy for a next-generation bone healing concept.
format article
author Lukas Otto
Petra Wolint
Annina Bopp
Anna Woloszyk
Anton S. Becker
Andreas Boss
Roland Böni
Maurizio Calcagni
Pietro Giovanoli
Simon P. Hoerstrup
Maximilian Y. Emmert
Johanna Buschmann
author_facet Lukas Otto
Petra Wolint
Annina Bopp
Anna Woloszyk
Anton S. Becker
Andreas Boss
Roland Böni
Maurizio Calcagni
Pietro Giovanoli
Simon P. Hoerstrup
Maximilian Y. Emmert
Johanna Buschmann
author_sort Lukas Otto
title 3D-microtissue derived secretome as a cell-free approach for enhanced mineralization of scaffolds in the chorioallantoic membrane model
title_short 3D-microtissue derived secretome as a cell-free approach for enhanced mineralization of scaffolds in the chorioallantoic membrane model
title_full 3D-microtissue derived secretome as a cell-free approach for enhanced mineralization of scaffolds in the chorioallantoic membrane model
title_fullStr 3D-microtissue derived secretome as a cell-free approach for enhanced mineralization of scaffolds in the chorioallantoic membrane model
title_full_unstemmed 3D-microtissue derived secretome as a cell-free approach for enhanced mineralization of scaffolds in the chorioallantoic membrane model
title_sort 3d-microtissue derived secretome as a cell-free approach for enhanced mineralization of scaffolds in the chorioallantoic membrane model
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/13a7a4e40eaf4c73bc17ec0a47a77cc5
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