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Engineered cell culture microenvironments for mechanobiology studies of brain neural cells

The biomechanical properties of the brain microenvironment, which is composed of different neural cell types, the extracellular matrix, and blood vessels, are critical for normal brain development and neural functioning. Stiffness, viscoelasticity and spatial organization of brain tissue modulate pr...

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Autores principales: Castillo Ransanz, Lucía, Van Altena, Pieter F. J., Heine, Vivi M., Accardo, Angelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794772/
https://www.ncbi.nlm.nih.gov/pubmed/36588937
http://dx.doi.org/10.3389/fbioe.2022.1096054
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author Castillo Ransanz, Lucía
Van Altena, Pieter F. J.
Heine, Vivi M.
Accardo, Angelo
author_facet Castillo Ransanz, Lucía
Van Altena, Pieter F. J.
Heine, Vivi M.
Accardo, Angelo
author_sort Castillo Ransanz, Lucía
collection PubMed
description The biomechanical properties of the brain microenvironment, which is composed of different neural cell types, the extracellular matrix, and blood vessels, are critical for normal brain development and neural functioning. Stiffness, viscoelasticity and spatial organization of brain tissue modulate proliferation, migration, differentiation, and cell function. However, the mechanical aspects of the neural microenvironment are largely ignored in current cell culture systems. Considering the high promises of human induced pluripotent stem cell- (iPSC-) based models for disease modelling and new treatment development, and in light of the physiological relevance of neuromechanobiological features, applications of in vitro engineered neuronal microenvironments should be explored thoroughly to develop more representative in vitro brain models. In this context, recently developed biomaterials in combination with micro- and nanofabrication techniques 1) allow investigating how mechanical properties affect neural cell development and functioning; 2) enable optimal cell microenvironment engineering strategies to advance neural cell models; and 3) provide a quantitative tool to assess changes in the neuromechanobiological properties of the brain microenvironment induced by pathology. In this review, we discuss the biological and engineering aspects involved in studying neuromechanobiology within scaffold-free and scaffold-based 2D and 3D iPSC-based brain models and approaches employing primary lineages (neural/glial), cell lines and other stem cells. Finally, we discuss future experimental directions of engineered microenvironments in neuroscience.
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spelling pubmed-97947722022-12-29 Engineered cell culture microenvironments for mechanobiology studies of brain neural cells Castillo Ransanz, Lucía Van Altena, Pieter F. J. Heine, Vivi M. Accardo, Angelo Front Bioeng Biotechnol Bioengineering and Biotechnology The biomechanical properties of the brain microenvironment, which is composed of different neural cell types, the extracellular matrix, and blood vessels, are critical for normal brain development and neural functioning. Stiffness, viscoelasticity and spatial organization of brain tissue modulate proliferation, migration, differentiation, and cell function. However, the mechanical aspects of the neural microenvironment are largely ignored in current cell culture systems. Considering the high promises of human induced pluripotent stem cell- (iPSC-) based models for disease modelling and new treatment development, and in light of the physiological relevance of neuromechanobiological features, applications of in vitro engineered neuronal microenvironments should be explored thoroughly to develop more representative in vitro brain models. In this context, recently developed biomaterials in combination with micro- and nanofabrication techniques 1) allow investigating how mechanical properties affect neural cell development and functioning; 2) enable optimal cell microenvironment engineering strategies to advance neural cell models; and 3) provide a quantitative tool to assess changes in the neuromechanobiological properties of the brain microenvironment induced by pathology. In this review, we discuss the biological and engineering aspects involved in studying neuromechanobiology within scaffold-free and scaffold-based 2D and 3D iPSC-based brain models and approaches employing primary lineages (neural/glial), cell lines and other stem cells. Finally, we discuss future experimental directions of engineered microenvironments in neuroscience. Frontiers Media S.A. 2022-12-14 /pmc/articles/PMC9794772/ /pubmed/36588937 http://dx.doi.org/10.3389/fbioe.2022.1096054 Text en Copyright © 2022 Castillo Ransanz, Van Altena, Heine and Accardo. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Castillo Ransanz, Lucía
Van Altena, Pieter F. J.
Heine, Vivi M.
Accardo, Angelo
Engineered cell culture microenvironments for mechanobiology studies of brain neural cells
title Engineered cell culture microenvironments for mechanobiology studies of brain neural cells
title_full Engineered cell culture microenvironments for mechanobiology studies of brain neural cells
title_fullStr Engineered cell culture microenvironments for mechanobiology studies of brain neural cells
title_full_unstemmed Engineered cell culture microenvironments for mechanobiology studies of brain neural cells
title_short Engineered cell culture microenvironments for mechanobiology studies of brain neural cells
title_sort engineered cell culture microenvironments for mechanobiology studies of brain neural cells
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794772/
https://www.ncbi.nlm.nih.gov/pubmed/36588937
http://dx.doi.org/10.3389/fbioe.2022.1096054
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