Hybrid spheroid microscaffolds as modular tissue units to build macro-tissue assemblies for tissue engineering.

High-resolution 3D printing Microscaffold Spheroids Stem cells Third tissue engineering strategy Two-photon polymerization

Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
15 Jul 2023
Historique:
received: 13 10 2021
revised: 02 03 2022
accepted: 07 03 2022
medline: 19 6 2023
pubmed: 16 3 2022
entrez: 15 3 2022
Statut: ppublish

Résumé

Since its inception, tissue engineering and regenerative medicine (TERM) has been relying on either scaffold-based or scaffold-free strategies. Recent reports outlined the possibility of a synergistic, convergence approach, referred to as the third TERM strategy, which could alleviate bottlenecks of the two previous options. This strategy requires the fabrication of highly porous microscaffolds, allowing to create single spheroids within each of them. The resulting tissue units can then be combined and used as modular building blocks for creating tissue constructs through a bottom-up self-assembly. Such strategy can have a significant impact for the future of TERM, but so far, no reports have assessed its feasibility in detail. This work reports a first systematic study, which includes a comparison of the in vitro behavior of tissue units based on adipose derived stem cell spheroids cultured within microscaffolds versus conventional spheroids. We first proved that the presence of the microscaffold neither impairs the cells 'ability to form spheroids nor impacts their viability. Importantly, the fusiogenic and the differentiation potential (i.e. chondrogenesis and osteogenesis), which are important features for cellularized building blocks to be used in TERM, are preserved when spheroids are cultured within microscaffolds. Significant benefits of microscaffold-based tissue units include the enhanced cell retention, the decreased compaction and the better control over the size observed when larger tissue constructs are formed through self-assembly. The proof of concept study presented here demonstrates the great potential offered by those microsize tissue units to be used as building blocks for directed tissue self-assembly. STATEMENT OF SIGNIFICANCE: One of the most exciting and recent advances in tissue engineering and regenerative medicine (TERM) is to combine together multiple micro-size cellularized units, which are able to self-assemble altogether to recreate larger tissue constructs. In this work, we produce such modules by forming single spheroids within highly porous microscaffolds, and study how this new microenvironment impacts on the spheroid's behavior and stemness potential. This work highlights as well that such novel route is enabled by two-photon polymerization, which is an additive manufacturing technique offering high spatial resolution down to 100 nm. These findings provide a first scientific evidence about the utilization of hybrid spheroid microscaffold-based tissue units with great perspective as a modular tool for TERM.

Identifiants

pubmed: 35288312
pii: S1742-7061(22)00141-6
doi: 10.1016/j.actbio.2022.03.010
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

72-85

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest . The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: A. Ovsianikov is a Co-Founder of UpNano GmbH, a recent spin-off of the TU Wien, which provided control software for the 2PP system. A. Arslan and S. Van Vlierberghe are in the founder team of BIO INX that commercializes Degrad INX.

Auteurs

Olivier Guillaume (O)

3D Printing and Biofabrication Group, Institute of Materials Science and Technology, TU Wien (Technische Universität Wien), Getreidemarkt 9/308, Vienna 1060, Austria; Austrian Cluster for Tissue Regeneration (http://www.tissue-regeneration.at), Austria.

Oliver Kopinski-Grünwald (O)

3D Printing and Biofabrication Group, Institute of Materials Science and Technology, TU Wien (Technische Universität Wien), Getreidemarkt 9/308, Vienna 1060, Austria; Austrian Cluster for Tissue Regeneration (http://www.tissue-regeneration.at), Austria.

Gregor Weisgrab (G)

3D Printing and Biofabrication Group, Institute of Materials Science and Technology, TU Wien (Technische Universität Wien), Getreidemarkt 9/308, Vienna 1060, Austria; Austrian Cluster for Tissue Regeneration (http://www.tissue-regeneration.at), Austria.

Theresia Baumgartner (T)

3D Printing and Biofabrication Group, Institute of Materials Science and Technology, TU Wien (Technische Universität Wien), Getreidemarkt 9/308, Vienna 1060, Austria.

Aysu Arslan (A)

Polymer Chemistry and Biomaterials Group, Centre of Macromolecular Chemistry, Department of Organic and Macromolecular Chemistry, Ghent University, Belgium.

Karin Whitmore (K)

University Service Center for Transmission Electron Microscopy, TU Wien, Austria.

Sandra Van Vlierberghe (S)

Polymer Chemistry and Biomaterials Group, Centre of Macromolecular Chemistry, Department of Organic and Macromolecular Chemistry, Ghent University, Belgium.

Aleksandr Ovsianikov (A)

3D Printing and Biofabrication Group, Institute of Materials Science and Technology, TU Wien (Technische Universität Wien), Getreidemarkt 9/308, Vienna 1060, Austria; Austrian Cluster for Tissue Regeneration (http://www.tissue-regeneration.at), Austria. Electronic address: aleksandr.ovsianikov@tuwien.ac.at.

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