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      Developmental GABA polarity switch and neuronal plasticity in Bioengineered Neuronal Organoids

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          Abstract

          Brain organoids are promising tools for disease modeling and drug development. For proper neuronal network formation excitatory and inhibitory neurons as well as glia need to co-develop. Here, we report the directed self-organization of human induced pluripotent stem cells in a collagen hydrogel towards a highly interconnected neuronal network at a macroscale tissue format. Bioengineered Neuronal Organoids (BENOs) comprise interconnected excitatory and inhibitory neurons with supportive astrocytes and oligodendrocytes. Giant depolarizing potential (GDP)-like events observed in early BENO cultures mimic early network activity of the fetal brain. The observed GABA polarity switch and reduced GDPs in >40 day BENO indicate progressive neuronal network maturation. BENOs demonstrate expedited complex network burst development after two months and evidence for long-term potentiation. The similarity of structural and functional properties to the fetal brain may allow for the application of BENOs in studies of neuronal plasticity and modeling of disease.

          Abstract

          Brain organoids are important tools to study early development and disease but little is known of their network activity and plasticity. Here the authors generate iPSC-derived neuronal organoids that display early network formation and maturation with evidence for a GABA polarity switch and long-term potentiation.

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          Most cited references23

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Synaptic plasticity, memory and the hippocampus: a neural network approach to causality.

            Two facts about the hippocampus have been common currency among neuroscientists for several decades. First, lesions of the hippocampus in humans prevent the acquisition of new episodic memories; second, activity-dependent synaptic plasticity is a prominent feature of hippocampal synapses. Given this background, the hypothesis that hippocampus-dependent memory is mediated, at least in part, by hippocampal synaptic plasticity has seemed as cogent in theory as it has been difficult to prove in practice. Here we argue that the recent development of transgenic molecular devices will encourage a shift from mechanistic investigations of synaptic plasticity in single neurons towards an analysis of how networks of neurons encode and represent memory, and we suggest ways in which this might be achieved. In the process, the hypothesis that synaptic plasticity is necessary and sufficient for information storage in the brain may finally be validated.
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              Guided self-organization and cortical plate formation in human brain organoids

              Engineering human brain organoids with floating scaffolds enhances the maturity and reproducibility of cortical tissue structure.
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                Author and article information

                Contributors
                patapia.zafeiriou@med.uni-goettingen.de
                w.zimmermann@med.uni-goettingen.de
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                29 July 2020
                29 July 2020
                2020
                : 11
                : 3791
                Affiliations
                [1 ]Institute of Pharmacology and Toxicology, University Medical Center, Georg-August-University, Göttingen, Germany
                [2 ]ISNI 0000 0004 5937 5237, GRID grid.452396.f, DZHK (German Center for Cardiovascular Research), partner site Göttingen, ; Göttingen, Germany
                [3 ]ISNI 0000 0001 2364 4210, GRID grid.7450.6, Cluster of Excellence “Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells” (MBExC), , University of Göttingen, ; Göttingen, Germany
                [4 ]Institute of Neurophysiology and Cellular Biophysics, University Medical Center, Georg-August-University, Göttingen, Germany
                [5 ]ISNI 0000 0001 2294 1395, GRID grid.1049.c, QIMR Berghofer Medical Research Institute, ; Brisbane, Australia
                [6 ]ISNI 0000 0001 2295 9843, GRID grid.16008.3f, Luxembourg Centre for Systems Biomedicine, , University of Luxembourg, ; 4365 Esch-sur-Alzette, Luxembourg
                [7 ]Department for Epigenetics and Systems Medicine in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE) Goettingen, 37075 Göttingen, Germany
                [8 ]Department of Psychiatry and Psychotherapy, University Medical Center, Georg-August-University, Göttingen, Germany
                Author information
                http://orcid.org/0000-0003-4604-4175
                http://orcid.org/0000-0003-0832-9356
                http://orcid.org/0000-0002-1402-1254
                http://orcid.org/0000-0003-2965-1491
                http://orcid.org/0000-0003-1190-4040
                Article
                17521
                10.1038/s41467-020-17521-w
                7391775
                32728089
                404cd7cb-66c1-4559-842d-362837da2171
                © The Author(s) 2020

                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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 27 November 2019
                : 2 July 2020
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                © The Author(s) 2020

                Uncategorized
                tissue engineering,developmental neurogenesis
                Uncategorized
                tissue engineering, developmental neurogenesis

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