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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2021
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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) |
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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 |
work_keys_str_mv |
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