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A microfabricated multi-compartment device for neuron and Schwann cell differentiation

Understanding the complex communication between different cell populations and their interaction with the microenvironment in the central and peripheral nervous systems is fundamental in neuroscience research. The development of appropriate in vitro approaches and tools, able to selectively analyze...

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Autores principales: De Vitis, Eleonora, La Pesa, Velia, Gervaso, Francesca, Romano, Alessandro, Quattrini, Angelo, Gigli, Giuseppe, Moroni, Lorenzo, Polini, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007719/
https://www.ncbi.nlm.nih.gov/pubmed/33782434
http://dx.doi.org/10.1038/s41598-021-86300-4
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author De Vitis, Eleonora
La Pesa, Velia
Gervaso, Francesca
Romano, Alessandro
Quattrini, Angelo
Gigli, Giuseppe
Moroni, Lorenzo
Polini, Alessandro
author_facet De Vitis, Eleonora
La Pesa, Velia
Gervaso, Francesca
Romano, Alessandro
Quattrini, Angelo
Gigli, Giuseppe
Moroni, Lorenzo
Polini, Alessandro
author_sort De Vitis, Eleonora
collection PubMed
description Understanding the complex communication between different cell populations and their interaction with the microenvironment in the central and peripheral nervous systems is fundamental in neuroscience research. The development of appropriate in vitro approaches and tools, able to selectively analyze and/or probe specific cells and cell portions (e.g., axons and cell bodies in neurons), driving their differentiation into specific cell phenotypes, has become therefore crucial in this direction. Here we report a multi-compartment microfluidic device where up to three different cell populations can be cultured in a fluidically independent circuit. The device allows cell migration across the compartments and their differentiation. We showed that an accurate choice of the device geometrical features and cell culture parameters allows to (1) maximize cell adhesion and proliferation of neuron-like human cells (SH-SY5Y cells), (2) control the inter-compartment cell migration of neuron and Schwann cells, (3) perform long-term cell culture studies in which both SH-SY5Y cells and primary rat Schwann cells can be differentiated towards specific phenotypes. These results can lead to a plethora of in vitro co-culture studies in the neuroscience research field, where tuning and investigating cell–cell and cell–microenvironment interactions are essential.
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spelling pubmed-80077192021-03-30 A microfabricated multi-compartment device for neuron and Schwann cell differentiation De Vitis, Eleonora La Pesa, Velia Gervaso, Francesca Romano, Alessandro Quattrini, Angelo Gigli, Giuseppe Moroni, Lorenzo Polini, Alessandro Sci Rep Article Understanding the complex communication between different cell populations and their interaction with the microenvironment in the central and peripheral nervous systems is fundamental in neuroscience research. The development of appropriate in vitro approaches and tools, able to selectively analyze and/or probe specific cells and cell portions (e.g., axons and cell bodies in neurons), driving their differentiation into specific cell phenotypes, has become therefore crucial in this direction. Here we report a multi-compartment microfluidic device where up to three different cell populations can be cultured in a fluidically independent circuit. The device allows cell migration across the compartments and their differentiation. We showed that an accurate choice of the device geometrical features and cell culture parameters allows to (1) maximize cell adhesion and proliferation of neuron-like human cells (SH-SY5Y cells), (2) control the inter-compartment cell migration of neuron and Schwann cells, (3) perform long-term cell culture studies in which both SH-SY5Y cells and primary rat Schwann cells can be differentiated towards specific phenotypes. These results can lead to a plethora of in vitro co-culture studies in the neuroscience research field, where tuning and investigating cell–cell and cell–microenvironment interactions are essential. Nature Publishing Group UK 2021-03-29 /pmc/articles/PMC8007719/ /pubmed/33782434 http://dx.doi.org/10.1038/s41598-021-86300-4 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
De Vitis, Eleonora
La Pesa, Velia
Gervaso, Francesca
Romano, Alessandro
Quattrini, Angelo
Gigli, Giuseppe
Moroni, Lorenzo
Polini, Alessandro
A microfabricated multi-compartment device for neuron and Schwann cell differentiation
title A microfabricated multi-compartment device for neuron and Schwann cell differentiation
title_full A microfabricated multi-compartment device for neuron and Schwann cell differentiation
title_fullStr A microfabricated multi-compartment device for neuron and Schwann cell differentiation
title_full_unstemmed A microfabricated multi-compartment device for neuron and Schwann cell differentiation
title_short A microfabricated multi-compartment device for neuron and Schwann cell differentiation
title_sort microfabricated multi-compartment device for neuron and schwann cell differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007719/
https://www.ncbi.nlm.nih.gov/pubmed/33782434
http://dx.doi.org/10.1038/s41598-021-86300-4
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