Comparison of Acute Effects of Neurotoxic Compounds on Network Activity in Human and Rodent Neural Cultures.

cell-based assays induced neurons induced pluripotent stem cells multielectrode arrays neural network activity neurotoxicity neurotoxicity screening

Journal

Toxicological sciences : an official journal of the Society of Toxicology
ISSN: 1096-0929
Titre abrégé: Toxicol Sci
Pays: United States
ID NLM: 9805461

Informations de publication

Date de publication:
12 04 2021
Historique:
pubmed: 5 2 2021
medline: 19 8 2021
entrez: 4 2 2021
Statut: ppublish

Résumé

Assessment of neuroactive effects of chemicals in cell-based assays remains challenging as complex functional tissue is required for biologically relevant readouts. Recent in vitro models using rodent primary neural cultures grown on multielectrode arrays allow quantitative measurements of neural network activity suitable for neurotoxicity screening. However, robust systems for testing effects on network function in human neural models are still lacking. The increasing number of differentiation protocols for generating neurons from human-induced pluripotent stem cells (hiPSCs) holds great potential to overcome the unavailability of human primary tissue and expedite cell-based assays. Yet, the variability in neuronal activity, prolonged ontogeny and rather immature stage of most neuronal cells derived by standard differentiation techniques greatly limit their utility for screening neurotoxic effects on human neural networks. Here, we used excitatory and inhibitory neurons, separately generated by direct reprogramming from hiPSCs, together with primary human astrocytes to establish highly functional cultures with defined cell ratios. Such neuron/glia cocultures exhibited pronounced neuronal activity and robust formation of synchronized network activity on multielectrode arrays, albeit with noticeable delay compared with primary rat cortical cultures. We further investigated acute changes of network activity in human neuron/glia cocultures and rat primary cortical cultures in response to compounds with known adverse neuroactive effects, including gamma amino butyric acid receptor antagonists and multiple pesticides. Importantly, we observed largely corresponding concentration-dependent effects on multiple neural network activity metrics using both neural culture types. These results demonstrate the utility of directly converted neuronal cells from hiPSCs for functional neurotoxicity screening of environmental chemicals.

Identifiants

pubmed: 33537736
pii: 6127535
doi: 10.1093/toxsci/kfab008
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

295-312

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Lorena Saavedra (L)

NeuCyte Inc., San Carlos, California 94070, USA.
Institute for Stem Cell Biology and Regenerative Medicine, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305, USA.

Kathleen Wallace (K)

BCTD, CCTE, ORD, US Environmental Protection Agency, Research Triangle Park, North Carolina 27711, USA.

Theresa F Freudenrich (TF)

BCTD, CCTE, ORD, US Environmental Protection Agency, Research Triangle Park, North Carolina 27711, USA.

Moritz Mall (M)

Institute for Stem Cell Biology and Regenerative Medicine, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305, USA.
Cell Fate Engineering and Disease Modeling Group, German Cancer Research Center (DKFZ) and DKFZ-ZMBH Alliance, Heidelberg 69120, Germany.

William R Mundy (WR)

BCTD, CCTE, ORD, US Environmental Protection Agency, Research Triangle Park, North Carolina 27711, USA.

Jorge Davila (J)

NeuCyte Inc., San Carlos, California 94070, USA.
Institute for Stem Cell Biology and Regenerative Medicine, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305, USA.

Timothy J Shafer (TJ)

BCTD, CCTE, ORD, US Environmental Protection Agency, Research Triangle Park, North Carolina 27711, USA.

Marius Wernig (M)

Institute for Stem Cell Biology and Regenerative Medicine, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305, USA.

Daniel Haag (D)

NeuCyte Inc., San Carlos, California 94070, USA.
Institute for Stem Cell Biology and Regenerative Medicine, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305, USA.

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