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Emergent structural and functional properties of hippocampal multi-cellular aggregates

Hippocampal neural networks are distinctly capable of integrating multi-modal sensory inputs to drive memory formation. Neuroscientific investigations using simplified in vitro models have greatly relied on planar (2D) neuronal cultures made from dissociated tissue. While these models have served as...

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Autores principales: Acero, Victor P., Das, Suradip, Rivellini, Olivia, Purvis, Erin M., Adewole, Dayo O., Cullen, Daniel Kacy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311220/
https://www.ncbi.nlm.nih.gov/pubmed/37397454
http://dx.doi.org/10.3389/fnins.2023.1171115
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author Acero, Victor P.
Das, Suradip
Rivellini, Olivia
Purvis, Erin M.
Adewole, Dayo O.
Cullen, Daniel Kacy
author_facet Acero, Victor P.
Das, Suradip
Rivellini, Olivia
Purvis, Erin M.
Adewole, Dayo O.
Cullen, Daniel Kacy
author_sort Acero, Victor P.
collection PubMed
description Hippocampal neural networks are distinctly capable of integrating multi-modal sensory inputs to drive memory formation. Neuroscientific investigations using simplified in vitro models have greatly relied on planar (2D) neuronal cultures made from dissociated tissue. While these models have served as simple, cost-effective, and high-throughput tools for examining various morphological and electrophysiological characteristics of hippocampal networks, 2D cultures fail to reconstitute critical elements of the brain microenvironment that may be necessary for the emergence of sophisticated integrative network properties. To address this, we utilized a forced aggregation technique to generate high-density (>100,000 cells/mm(3)) multi-cellular three-dimensional aggregates using rodent embryonic hippocampal tissue. We contrasted the emergent structural and functional properties of aggregated (3D) and dissociated (2D) cultures over 28 days in vitro (DIV). Hippocampal aggregates displayed robust axonal fasciculation across large distances and significant neuronal polarization, i.e., spatial segregation of dendrites and axons, at earlier time points compared to dissociated cultures. Moreover, we found that astrocytes in aggregate cultures self-organized into non-overlapping quasi-domains and developed highly stellate morphologies resembling astrocyte structures in vivo. We maintained cultures on multi-electrode arrays (MEAs) to assess spontaneous electrophysiological activity for up to 28 DIV. We found that 3D networks of aggregated cultures developed highly synchronized networks and with high burstiness by 28 DIV. We also demonstrated that dual-aggregate networks became active by 7 DIV, in contrast to single-aggregate networks which became active and developed synchronous bursting activity with repeating motifs by 14 DIV. Taken together, our findings demonstrate that the high-density, multi-cellular, 3D microenvironment of hippocampal aggregates supports the recapitulation of emergent biofidelic morphological and functional properties. Our findings suggest that neural aggregates may be used as segregated, modular building blocks for the development of complex, multi-nodal neural network topologies.
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spelling pubmed-103112202023-07-01 Emergent structural and functional properties of hippocampal multi-cellular aggregates Acero, Victor P. Das, Suradip Rivellini, Olivia Purvis, Erin M. Adewole, Dayo O. Cullen, Daniel Kacy Front Neurosci Neuroscience Hippocampal neural networks are distinctly capable of integrating multi-modal sensory inputs to drive memory formation. Neuroscientific investigations using simplified in vitro models have greatly relied on planar (2D) neuronal cultures made from dissociated tissue. While these models have served as simple, cost-effective, and high-throughput tools for examining various morphological and electrophysiological characteristics of hippocampal networks, 2D cultures fail to reconstitute critical elements of the brain microenvironment that may be necessary for the emergence of sophisticated integrative network properties. To address this, we utilized a forced aggregation technique to generate high-density (>100,000 cells/mm(3)) multi-cellular three-dimensional aggregates using rodent embryonic hippocampal tissue. We contrasted the emergent structural and functional properties of aggregated (3D) and dissociated (2D) cultures over 28 days in vitro (DIV). Hippocampal aggregates displayed robust axonal fasciculation across large distances and significant neuronal polarization, i.e., spatial segregation of dendrites and axons, at earlier time points compared to dissociated cultures. Moreover, we found that astrocytes in aggregate cultures self-organized into non-overlapping quasi-domains and developed highly stellate morphologies resembling astrocyte structures in vivo. We maintained cultures on multi-electrode arrays (MEAs) to assess spontaneous electrophysiological activity for up to 28 DIV. We found that 3D networks of aggregated cultures developed highly synchronized networks and with high burstiness by 28 DIV. We also demonstrated that dual-aggregate networks became active by 7 DIV, in contrast to single-aggregate networks which became active and developed synchronous bursting activity with repeating motifs by 14 DIV. Taken together, our findings demonstrate that the high-density, multi-cellular, 3D microenvironment of hippocampal aggregates supports the recapitulation of emergent biofidelic morphological and functional properties. Our findings suggest that neural aggregates may be used as segregated, modular building blocks for the development of complex, multi-nodal neural network topologies. Frontiers Media S.A. 2023-06-15 /pmc/articles/PMC10311220/ /pubmed/37397454 http://dx.doi.org/10.3389/fnins.2023.1171115 Text en Copyright © 2023 Acero, Das, Rivellini, Purvis, Adewole and Cullen. 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 Neuroscience
Acero, Victor P.
Das, Suradip
Rivellini, Olivia
Purvis, Erin M.
Adewole, Dayo O.
Cullen, Daniel Kacy
Emergent structural and functional properties of hippocampal multi-cellular aggregates
title Emergent structural and functional properties of hippocampal multi-cellular aggregates
title_full Emergent structural and functional properties of hippocampal multi-cellular aggregates
title_fullStr Emergent structural and functional properties of hippocampal multi-cellular aggregates
title_full_unstemmed Emergent structural and functional properties of hippocampal multi-cellular aggregates
title_short Emergent structural and functional properties of hippocampal multi-cellular aggregates
title_sort emergent structural and functional properties of hippocampal multi-cellular aggregates
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311220/
https://www.ncbi.nlm.nih.gov/pubmed/37397454
http://dx.doi.org/10.3389/fnins.2023.1171115
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