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Scientific Validation of Human Neurosphere Assays for Developmental Neurotoxicity Evaluation

There is a call for a paradigm shift in developmental neurotoxicity (DNT) evaluation, which demands the implementation of faster, more cost-efficient, and human-relevant test systems than current in vivo guideline studies. Under the umbrella of the Organisation for Economic Co-operation and Developm...

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Autores principales: Koch, Katharina, Bartmann, Kristina, Hartmann, Julia, Kapr, Julia, Klose, Jördis, Kuchovská, Eliška, Pahl, Melanie, Schlüppmann, Kevin, Zühr, Etta, Fritsche, Ellen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8915868/
https://www.ncbi.nlm.nih.gov/pubmed/35295221
http://dx.doi.org/10.3389/ftox.2022.816370
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author Koch, Katharina
Bartmann, Kristina
Hartmann, Julia
Kapr, Julia
Klose, Jördis
Kuchovská, Eliška
Pahl, Melanie
Schlüppmann, Kevin
Zühr, Etta
Fritsche, Ellen
author_facet Koch, Katharina
Bartmann, Kristina
Hartmann, Julia
Kapr, Julia
Klose, Jördis
Kuchovská, Eliška
Pahl, Melanie
Schlüppmann, Kevin
Zühr, Etta
Fritsche, Ellen
author_sort Koch, Katharina
collection PubMed
description There is a call for a paradigm shift in developmental neurotoxicity (DNT) evaluation, which demands the implementation of faster, more cost-efficient, and human-relevant test systems than current in vivo guideline studies. Under the umbrella of the Organisation for Economic Co-operation and Development (OECD), a guidance document is currently being prepared that instructs on the regulatory use of a DNT in vitro battery (DNT IVB) for fit-for-purpose applications. One crucial issue for OECD application of methods is validation, which for new approach methods (NAMs) requires novel approaches. Here, mechanistic information previously identified in vivo, as well as reported neurodevelopmental adversities in response to disturbances on the cellular and tissue level, are of central importance. In this study, we scientifically validate the Neurosphere Assay, which is based on human primary neural progenitor cells (hNPCs) and an integral part of the DNT IVB. It assesses neurodevelopmental key events (KEs) like NPC proliferation (NPC1ab), radial glia cell migration (NPC2a), neuronal differentiation (NPC3), neurite outgrowth (NPC4), oligodendrocyte differentiation (NPC5), and thyroid hormone-dependent oligodendrocyte maturation (NPC6). In addition, we extend our work from the hNPCs to human induced pluripotent stem cell-derived NPCs (hiNPCs) for the NPC proliferation (iNPC1ab) and radial glia assays (iNPC2a). The validation process we report for the endpoints studied with the Neurosphere Assays is based on 1) describing the relevance of the respective endpoints for brain development, 2) the confirmation of the cell type-specific morphologies observed in vitro, 3) expressions of cell type-specific markers consistent with those morphologies, 4) appropriate anticipated responses to physiological pertinent signaling stimuli and 5) alterations in specific in vitro endpoints upon challenges with confirmed DNT compounds. With these strong mechanistic underpinnings, we posit that the Neurosphere Assay as an integral part of the DNT in vitro screening battery is well poised for DNT evaluation for regulatory purposes.
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spelling pubmed-89158682022-03-15 Scientific Validation of Human Neurosphere Assays for Developmental Neurotoxicity Evaluation Koch, Katharina Bartmann, Kristina Hartmann, Julia Kapr, Julia Klose, Jördis Kuchovská, Eliška Pahl, Melanie Schlüppmann, Kevin Zühr, Etta Fritsche, Ellen Front Toxicol Toxicology There is a call for a paradigm shift in developmental neurotoxicity (DNT) evaluation, which demands the implementation of faster, more cost-efficient, and human-relevant test systems than current in vivo guideline studies. Under the umbrella of the Organisation for Economic Co-operation and Development (OECD), a guidance document is currently being prepared that instructs on the regulatory use of a DNT in vitro battery (DNT IVB) for fit-for-purpose applications. One crucial issue for OECD application of methods is validation, which for new approach methods (NAMs) requires novel approaches. Here, mechanistic information previously identified in vivo, as well as reported neurodevelopmental adversities in response to disturbances on the cellular and tissue level, are of central importance. In this study, we scientifically validate the Neurosphere Assay, which is based on human primary neural progenitor cells (hNPCs) and an integral part of the DNT IVB. It assesses neurodevelopmental key events (KEs) like NPC proliferation (NPC1ab), radial glia cell migration (NPC2a), neuronal differentiation (NPC3), neurite outgrowth (NPC4), oligodendrocyte differentiation (NPC5), and thyroid hormone-dependent oligodendrocyte maturation (NPC6). In addition, we extend our work from the hNPCs to human induced pluripotent stem cell-derived NPCs (hiNPCs) for the NPC proliferation (iNPC1ab) and radial glia assays (iNPC2a). The validation process we report for the endpoints studied with the Neurosphere Assays is based on 1) describing the relevance of the respective endpoints for brain development, 2) the confirmation of the cell type-specific morphologies observed in vitro, 3) expressions of cell type-specific markers consistent with those morphologies, 4) appropriate anticipated responses to physiological pertinent signaling stimuli and 5) alterations in specific in vitro endpoints upon challenges with confirmed DNT compounds. With these strong mechanistic underpinnings, we posit that the Neurosphere Assay as an integral part of the DNT in vitro screening battery is well poised for DNT evaluation for regulatory purposes. Frontiers Media S.A. 2022-03-02 /pmc/articles/PMC8915868/ /pubmed/35295221 http://dx.doi.org/10.3389/ftox.2022.816370 Text en Copyright © 2022 Koch, Bartmann, Hartmann, Kapr, Klose, Kuchovská, Pahl, Schlüppmann, Zühr and Fritsche. 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 Toxicology
Koch, Katharina
Bartmann, Kristina
Hartmann, Julia
Kapr, Julia
Klose, Jördis
Kuchovská, Eliška
Pahl, Melanie
Schlüppmann, Kevin
Zühr, Etta
Fritsche, Ellen
Scientific Validation of Human Neurosphere Assays for Developmental Neurotoxicity Evaluation
title Scientific Validation of Human Neurosphere Assays for Developmental Neurotoxicity Evaluation
title_full Scientific Validation of Human Neurosphere Assays for Developmental Neurotoxicity Evaluation
title_fullStr Scientific Validation of Human Neurosphere Assays for Developmental Neurotoxicity Evaluation
title_full_unstemmed Scientific Validation of Human Neurosphere Assays for Developmental Neurotoxicity Evaluation
title_short Scientific Validation of Human Neurosphere Assays for Developmental Neurotoxicity Evaluation
title_sort scientific validation of human neurosphere assays for developmental neurotoxicity evaluation
topic Toxicology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8915868/
https://www.ncbi.nlm.nih.gov/pubmed/35295221
http://dx.doi.org/10.3389/ftox.2022.816370
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