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Organs to Cells and Cells to Organoids: The Evolution of in vitro Central Nervous System Modelling

With 100 billion neurons and 100 trillion synapses, the human brain is not just the most complex organ in the human body, but has also been described as “the most complex thing in the universe.” The limited availability of human living brain tissue for the study of neurogenesis, neural processes and...

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Autores principales: Pacitti, Dario, Privolizzi, Riccardo, Bax, Bridget E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465581/
https://www.ncbi.nlm.nih.gov/pubmed/31024259
http://dx.doi.org/10.3389/fncel.2019.00129
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author Pacitti, Dario
Privolizzi, Riccardo
Bax, Bridget E.
author_facet Pacitti, Dario
Privolizzi, Riccardo
Bax, Bridget E.
author_sort Pacitti, Dario
collection PubMed
description With 100 billion neurons and 100 trillion synapses, the human brain is not just the most complex organ in the human body, but has also been described as “the most complex thing in the universe.” The limited availability of human living brain tissue for the study of neurogenesis, neural processes and neurological disorders has resulted in more than a century-long strive from researchers worldwide to model the central nervous system (CNS) and dissect both its striking physiology and enigmatic pathophysiology. The invaluable knowledge gained with the use of animal models and post mortem human tissue remains limited to cross-species similarities and structural features, respectively. The advent of human induced pluripotent stem cell (hiPSC) and 3-D organoid technologies has revolutionised the approach to the study of human brain and CNS in vitro, presenting great potential for disease modelling and translational adoption in drug screening and regenerative medicine, also contributing beneficially to clinical research. We have surveyed more than 100 years of research in CNS modelling and provide in this review an historical excursus of its evolution, from early neural tissue explants and organotypic cultures, to 2-D patient-derived cell monolayers, to the latest development of 3-D cerebral organoids. We have generated a comprehensive summary of CNS modelling techniques and approaches, protocol refinements throughout the course of decades and developments in the study of specific neuropathologies. Current limitations and caveats such as clonal variation, developmental stage, validation of pluripotency and chromosomal stability, functional assessment, reproducibility, accuracy and scalability of these models are also discussed.
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spelling pubmed-64655812019-04-25 Organs to Cells and Cells to Organoids: The Evolution of in vitro Central Nervous System Modelling Pacitti, Dario Privolizzi, Riccardo Bax, Bridget E. Front Cell Neurosci Neuroscience With 100 billion neurons and 100 trillion synapses, the human brain is not just the most complex organ in the human body, but has also been described as “the most complex thing in the universe.” The limited availability of human living brain tissue for the study of neurogenesis, neural processes and neurological disorders has resulted in more than a century-long strive from researchers worldwide to model the central nervous system (CNS) and dissect both its striking physiology and enigmatic pathophysiology. The invaluable knowledge gained with the use of animal models and post mortem human tissue remains limited to cross-species similarities and structural features, respectively. The advent of human induced pluripotent stem cell (hiPSC) and 3-D organoid technologies has revolutionised the approach to the study of human brain and CNS in vitro, presenting great potential for disease modelling and translational adoption in drug screening and regenerative medicine, also contributing beneficially to clinical research. We have surveyed more than 100 years of research in CNS modelling and provide in this review an historical excursus of its evolution, from early neural tissue explants and organotypic cultures, to 2-D patient-derived cell monolayers, to the latest development of 3-D cerebral organoids. We have generated a comprehensive summary of CNS modelling techniques and approaches, protocol refinements throughout the course of decades and developments in the study of specific neuropathologies. Current limitations and caveats such as clonal variation, developmental stage, validation of pluripotency and chromosomal stability, functional assessment, reproducibility, accuracy and scalability of these models are also discussed. Frontiers Media S.A. 2019-04-09 /pmc/articles/PMC6465581/ /pubmed/31024259 http://dx.doi.org/10.3389/fncel.2019.00129 Text en Copyright © 2019 Pacitti, Privolizzi and Bax. http://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 Neuroscience
Pacitti, Dario
Privolizzi, Riccardo
Bax, Bridget E.
Organs to Cells and Cells to Organoids: The Evolution of in vitro Central Nervous System Modelling
title Organs to Cells and Cells to Organoids: The Evolution of in vitro Central Nervous System Modelling
title_full Organs to Cells and Cells to Organoids: The Evolution of in vitro Central Nervous System Modelling
title_fullStr Organs to Cells and Cells to Organoids: The Evolution of in vitro Central Nervous System Modelling
title_full_unstemmed Organs to Cells and Cells to Organoids: The Evolution of in vitro Central Nervous System Modelling
title_short Organs to Cells and Cells to Organoids: The Evolution of in vitro Central Nervous System Modelling
title_sort organs to cells and cells to organoids: the evolution of in vitro central nervous system modelling
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465581/
https://www.ncbi.nlm.nih.gov/pubmed/31024259
http://dx.doi.org/10.3389/fncel.2019.00129
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