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

Pacitti, D; Privolizzi, R; Bax, BE (2019) Organs to Cells and Cells to Organoids: The Evolution of in vitro Central Nervous System Modelling. FRONTIERS IN CELLULAR NEUROSCIENCE, 13 (129). ISSN 1662-5102 https://doi.org/10.3389/fncel.2019.00129
SGUL Authors: Bax, Bridget Elizabeth

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Abstract

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.

Item Type: Article
Additional Information: © 2019 Pacitti, Privolizzi and Bax. 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.
Keywords: CNS, hiPSC, human neurons, human glia, neurogenesis, neurological disorders, cerebral organoids, organotypic
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: FRONTIERS IN CELLULAR NEUROSCIENCE
ISSN: 1662-5102
Dates:
DateEvent
9 April 2019Published
14 March 2019Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
PUMPA14Purine Metabolic Patients AssociationUNSPECIFIED
K025406/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
Web of Science ID: WOS:000463966600001
URI: https://openaccess.sgul.ac.uk/id/eprint/110761
Publisher's version: https://doi.org/10.3389/fncel.2019.00129

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