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A pesticide and iPSC dopaminergic neuron screen identifies and classifies Parkinson-relevant pesticides
Parkinson’s disease (PD) is a complex neurodegenerative disease with etiology rooted in genetic vulnerability and environmental factors. Here we combine quantitative epidemiologic study of pesticide exposures and PD with toxicity screening in dopaminergic neurons derived from PD patient induced plur...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10188516/ https://www.ncbi.nlm.nih.gov/pubmed/37193692 http://dx.doi.org/10.1038/s41467-023-38215-z |
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author | Paul, Kimberly C. Krolewski, Richard C. Lucumi Moreno, Edinson Blank, Jack Holton, Kristina M. Ahfeldt, Tim Furlong, Melissa Yu, Yu Cockburn, Myles Thompson, Laura K. Kreymerman, Alexander Ricci-Blair, Elisabeth M. Li, Yu Jun Patel, Heer B. Lee, Richard T. Bronstein, Jeff Rubin, Lee L. Khurana, Vikram Ritz, Beate |
author_facet | Paul, Kimberly C. Krolewski, Richard C. Lucumi Moreno, Edinson Blank, Jack Holton, Kristina M. Ahfeldt, Tim Furlong, Melissa Yu, Yu Cockburn, Myles Thompson, Laura K. Kreymerman, Alexander Ricci-Blair, Elisabeth M. Li, Yu Jun Patel, Heer B. Lee, Richard T. Bronstein, Jeff Rubin, Lee L. Khurana, Vikram Ritz, Beate |
author_sort | Paul, Kimberly C. |
collection | PubMed |
description | Parkinson’s disease (PD) is a complex neurodegenerative disease with etiology rooted in genetic vulnerability and environmental factors. Here we combine quantitative epidemiologic study of pesticide exposures and PD with toxicity screening in dopaminergic neurons derived from PD patient induced pluripotent stem cells (iPSCs) to identify Parkinson’s-relevant pesticides. Agricultural records enable investigation of 288 specific pesticides and PD risk in a comprehensive, pesticide-wide association study. We associate long-term exposure to 53 pesticides with PD and identify co-exposure profiles. We then employ a live-cell imaging screening paradigm exposing dopaminergic neurons to 39 PD-associated pesticides. We find that 10 pesticides are directly toxic to these neurons. Further, we analyze pesticides typically used in combinations in cotton farming, demonstrating that co-exposures result in greater toxicity than any single pesticide. We find trifluralin is a driver of toxicity to dopaminergic neurons and leads to mitochondrial dysfunction. Our paradigm may prove useful to mechanistically dissect pesticide exposures implicated in PD risk and guide agricultural policy. |
format | Online Article Text |
id | pubmed-10188516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101885162023-05-18 A pesticide and iPSC dopaminergic neuron screen identifies and classifies Parkinson-relevant pesticides Paul, Kimberly C. Krolewski, Richard C. Lucumi Moreno, Edinson Blank, Jack Holton, Kristina M. Ahfeldt, Tim Furlong, Melissa Yu, Yu Cockburn, Myles Thompson, Laura K. Kreymerman, Alexander Ricci-Blair, Elisabeth M. Li, Yu Jun Patel, Heer B. Lee, Richard T. Bronstein, Jeff Rubin, Lee L. Khurana, Vikram Ritz, Beate Nat Commun Article Parkinson’s disease (PD) is a complex neurodegenerative disease with etiology rooted in genetic vulnerability and environmental factors. Here we combine quantitative epidemiologic study of pesticide exposures and PD with toxicity screening in dopaminergic neurons derived from PD patient induced pluripotent stem cells (iPSCs) to identify Parkinson’s-relevant pesticides. Agricultural records enable investigation of 288 specific pesticides and PD risk in a comprehensive, pesticide-wide association study. We associate long-term exposure to 53 pesticides with PD and identify co-exposure profiles. We then employ a live-cell imaging screening paradigm exposing dopaminergic neurons to 39 PD-associated pesticides. We find that 10 pesticides are directly toxic to these neurons. Further, we analyze pesticides typically used in combinations in cotton farming, demonstrating that co-exposures result in greater toxicity than any single pesticide. We find trifluralin is a driver of toxicity to dopaminergic neurons and leads to mitochondrial dysfunction. Our paradigm may prove useful to mechanistically dissect pesticide exposures implicated in PD risk and guide agricultural policy. Nature Publishing Group UK 2023-05-16 /pmc/articles/PMC10188516/ /pubmed/37193692 http://dx.doi.org/10.1038/s41467-023-38215-z Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Paul, Kimberly C. Krolewski, Richard C. Lucumi Moreno, Edinson Blank, Jack Holton, Kristina M. Ahfeldt, Tim Furlong, Melissa Yu, Yu Cockburn, Myles Thompson, Laura K. Kreymerman, Alexander Ricci-Blair, Elisabeth M. Li, Yu Jun Patel, Heer B. Lee, Richard T. Bronstein, Jeff Rubin, Lee L. Khurana, Vikram Ritz, Beate A pesticide and iPSC dopaminergic neuron screen identifies and classifies Parkinson-relevant pesticides |
title | A pesticide and iPSC dopaminergic neuron screen identifies and classifies Parkinson-relevant pesticides |
title_full | A pesticide and iPSC dopaminergic neuron screen identifies and classifies Parkinson-relevant pesticides |
title_fullStr | A pesticide and iPSC dopaminergic neuron screen identifies and classifies Parkinson-relevant pesticides |
title_full_unstemmed | A pesticide and iPSC dopaminergic neuron screen identifies and classifies Parkinson-relevant pesticides |
title_short | A pesticide and iPSC dopaminergic neuron screen identifies and classifies Parkinson-relevant pesticides |
title_sort | pesticide and ipsc dopaminergic neuron screen identifies and classifies parkinson-relevant pesticides |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10188516/ https://www.ncbi.nlm.nih.gov/pubmed/37193692 http://dx.doi.org/10.1038/s41467-023-38215-z |
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