Novel method to produce a layered 3D scaffold for human pluripotent stem cell-derived neuronal cells.

Collagen 1 Electrospinning Guidance cue Hydrogel Polylactide Tissue engineering

Journal

Journal of neuroscience methods
ISSN: 1872-678X
Titre abrégé: J Neurosci Methods
Pays: Netherlands
ID NLM: 7905558

Informations de publication

Date de publication:
15 02 2021
Historique:
received: 10 07 2020
revised: 10 12 2020
accepted: 11 12 2020
pubmed: 22 12 2020
medline: 1 7 2021
entrez: 21 12 2020
Statut: ppublish

Résumé

Three-dimensional (3D) in vitro models have been developed into more in vivo resembling structures. In particular, there is a need for human-based models for neuronal tissue engineering (TE). To produce such a model with organized microenvironment for cells in central nervous system (CNS), a 3D layered scaffold composed of hydrogel and cell guiding fibers has been proposed. Here, we describe a novel method for producing a layered 3D scaffold consisting of electrospun poly (L,D-lactide) fibers embedded into collagen 1 hydrogel to achieve better resemblance of cells' natural microenvironment for human pluripotent stem cell (hPSC)-derived neurons. The scaffold was constructed via a single layer-by-layer process using an electrospinning technique with a unique collector design. The method enabled the production of layered 3D cell-containing scaffold in a single process. HPSC-derived neurons were found in all layers of the scaffold and exhibited a typical neuronal phenotype. The guiding fiber layers supported the directed cell growth and extension of the neurites inside the scaffold without additional functionalization. Previous methods have required several process steps to construct 3D layer-by-layer scaffolds. We introduced a method to produce layered 3D scaffolds to mimic the cell guiding cues in CNS by alternating the soft hydrogel matrix and fibrous guidance cues. The produced scaffold successfully enabled the long-term culture of hPSC-derived neuronal cells. This layered 3D scaffold is a useful model for in vitro and in vivo neuronal TE applications.

Sections du résumé

BACKGROUND
Three-dimensional (3D) in vitro models have been developed into more in vivo resembling structures. In particular, there is a need for human-based models for neuronal tissue engineering (TE). To produce such a model with organized microenvironment for cells in central nervous system (CNS), a 3D layered scaffold composed of hydrogel and cell guiding fibers has been proposed.
NEW METHOD
Here, we describe a novel method for producing a layered 3D scaffold consisting of electrospun poly (L,D-lactide) fibers embedded into collagen 1 hydrogel to achieve better resemblance of cells' natural microenvironment for human pluripotent stem cell (hPSC)-derived neurons. The scaffold was constructed via a single layer-by-layer process using an electrospinning technique with a unique collector design.
RESULTS
The method enabled the production of layered 3D cell-containing scaffold in a single process. HPSC-derived neurons were found in all layers of the scaffold and exhibited a typical neuronal phenotype. The guiding fiber layers supported the directed cell growth and extension of the neurites inside the scaffold without additional functionalization.
COMPARISON WITH EXISTING METHODS
Previous methods have required several process steps to construct 3D layer-by-layer scaffolds.
CONCLUSIONS
We introduced a method to produce layered 3D scaffolds to mimic the cell guiding cues in CNS by alternating the soft hydrogel matrix and fibrous guidance cues. The produced scaffold successfully enabled the long-term culture of hPSC-derived neuronal cells. This layered 3D scaffold is a useful model for in vitro and in vivo neuronal TE applications.

Identifiants

pubmed: 33345946
pii: S0165-0270(20)30466-0
doi: 10.1016/j.jneumeth.2020.109043
pii:
doi:

Substances chimiques

Hydrogels 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

109043

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Laura Honkamäki (L)

NeuroGroup, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland. Electronic address: laura.honkamaki@tuni.fi.

Tiina Joki (T)

NeuroGroup, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.

Nikita A Grigoryev (NA)

Department of Chemical and Biomolecular Engineering, NYU Tandon School of Engineering, Brooklyn, NY, USA.

Kalle Levon (K)

Department of Chemical and Biomolecular Engineering, NYU Tandon School of Engineering, Brooklyn, NY, USA.

Laura Ylä-Outinen (L)

NeuroGroup, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.

Susanna Narkilahti (S)

NeuroGroup, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.

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