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Review: In vitro Cell Platform for Understanding Developmental Toxicity
Developmental toxicity and its affiliation to long-term health, particularly neurodegenerative disease (ND) has attracted significant attentions in recent years. There is, however, a significant gap in current models to track longitudinal changes arising from developmental toxicity. The advent of in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7785584/ https://www.ncbi.nlm.nih.gov/pubmed/33424939 http://dx.doi.org/10.3389/fgene.2020.623117 |
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author | Xie, Junkai Wettschurack, Kyle Yuan, Chongli |
author_facet | Xie, Junkai Wettschurack, Kyle Yuan, Chongli |
author_sort | Xie, Junkai |
collection | PubMed |
description | Developmental toxicity and its affiliation to long-term health, particularly neurodegenerative disease (ND) has attracted significant attentions in recent years. There is, however, a significant gap in current models to track longitudinal changes arising from developmental toxicity. The advent of induced pluripotent stem cell (iPSC) derived neuronal culture has allowed for more complex and functionally active in vitro neuronal models. Coupled with recent progress in the detection of ND biomarkers, we are equipped with promising new tools to understand neurotoxicity arising from developmental exposure. This review provides a brief overview of current progress in neuronal culture derived from iPSC and in ND markers. |
format | Online Article Text |
id | pubmed-7785584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77855842021-01-07 Review: In vitro Cell Platform for Understanding Developmental Toxicity Xie, Junkai Wettschurack, Kyle Yuan, Chongli Front Genet Genetics Developmental toxicity and its affiliation to long-term health, particularly neurodegenerative disease (ND) has attracted significant attentions in recent years. There is, however, a significant gap in current models to track longitudinal changes arising from developmental toxicity. The advent of induced pluripotent stem cell (iPSC) derived neuronal culture has allowed for more complex and functionally active in vitro neuronal models. Coupled with recent progress in the detection of ND biomarkers, we are equipped with promising new tools to understand neurotoxicity arising from developmental exposure. This review provides a brief overview of current progress in neuronal culture derived from iPSC and in ND markers. Frontiers Media S.A. 2020-12-23 /pmc/articles/PMC7785584/ /pubmed/33424939 http://dx.doi.org/10.3389/fgene.2020.623117 Text en Copyright © 2020 Xie, Wettschurack and Yuan. http://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 | Genetics Xie, Junkai Wettschurack, Kyle Yuan, Chongli Review: In vitro Cell Platform for Understanding Developmental Toxicity |
title | Review: In vitro Cell Platform for Understanding Developmental Toxicity |
title_full | Review: In vitro Cell Platform for Understanding Developmental Toxicity |
title_fullStr | Review: In vitro Cell Platform for Understanding Developmental Toxicity |
title_full_unstemmed | Review: In vitro Cell Platform for Understanding Developmental Toxicity |
title_short | Review: In vitro Cell Platform for Understanding Developmental Toxicity |
title_sort | review: in vitro cell platform for understanding developmental toxicity |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7785584/ https://www.ncbi.nlm.nih.gov/pubmed/33424939 http://dx.doi.org/10.3389/fgene.2020.623117 |
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