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Environmental Toxin Screening Using Human-Derived 3D Bioengineered Liver and Cardiac Organoids

INTRODUCTION: Environmental toxins, such as lead and other heavy metals, pesticides, and other compounds, represent a significant health concern within the USA and around the world. Even in the twenty-first century, a plethora of cities and towns in the U.S. have suffered from exposures to lead in d...

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Autores principales: Forsythe, Steven D., Devarasetty, Mahesh, Shupe, Thomas, Bishop, Colin, Atala, Anthony, Soker, Shay, Skardal, Aleksander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5932352/
https://www.ncbi.nlm.nih.gov/pubmed/29755963
http://dx.doi.org/10.3389/fpubh.2018.00103
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author Forsythe, Steven D.
Devarasetty, Mahesh
Shupe, Thomas
Bishop, Colin
Atala, Anthony
Soker, Shay
Skardal, Aleksander
author_facet Forsythe, Steven D.
Devarasetty, Mahesh
Shupe, Thomas
Bishop, Colin
Atala, Anthony
Soker, Shay
Skardal, Aleksander
author_sort Forsythe, Steven D.
collection PubMed
description INTRODUCTION: Environmental toxins, such as lead and other heavy metals, pesticides, and other compounds, represent a significant health concern within the USA and around the world. Even in the twenty-first century, a plethora of cities and towns in the U.S. have suffered from exposures to lead in drinking water or other heavy metals in food or the earth, while there is a high possibility of further places to suffer such exposures in the near future. METHODS: We employed bioengineered 3D human liver and cardiac organoids to screen a panel of environmental toxins (lead, mercury, thallium, and glyphosate), and charted the response of the organoids to these compounds. Liver and cardiac organoids were exposed to lead (10 µM–10 mM), mercury (200 nM–200 µM), thallium (10 nM–10 µM), or glyphosate (25 µM–25 mM) for a duration of 48 h. The impacts of toxin exposure were then assessed by LIVE/DEAD viability and cytotoxicity staining, measuring ATP activity and determining IC50 values, and determining changes in cardiac organoid beating activity. RESULTS: As expected, all of the toxins induced toxicity in the organoids. Both ATP and LIVE/DEAD assays showed toxicity in both liver and cardiac organoids. In particular, thallium was the most toxic, with IC50 values of 13.5 and 1.35 µM in liver and cardiac organoids, respectively. Conversely, glyphosate was the least toxic of the four compounds, with IC50 values of 10.53 and 10.85 mM in liver and cardiac organoids, respectively. Additionally, toxins had a negative influence on cardiac organoid beating activity as well. Thallium resulting in the most significant decreases in beating rate, followed by mercury, then glyphosate, and finally, lead. These results suggest that the 3D organoids have significant utility to be deployed in additional toxicity screening applications, and future development of treatments to mitigate exposures. CONCLUSION: 3D organoids have significant utility to be deployed in additional toxicity screening applications, such as future development of treatments to mitigate exposures, drug screening, and environmental toxin detection.
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spelling pubmed-59323522018-05-11 Environmental Toxin Screening Using Human-Derived 3D Bioengineered Liver and Cardiac Organoids Forsythe, Steven D. Devarasetty, Mahesh Shupe, Thomas Bishop, Colin Atala, Anthony Soker, Shay Skardal, Aleksander Front Public Health Public Health INTRODUCTION: Environmental toxins, such as lead and other heavy metals, pesticides, and other compounds, represent a significant health concern within the USA and around the world. Even in the twenty-first century, a plethora of cities and towns in the U.S. have suffered from exposures to lead in drinking water or other heavy metals in food or the earth, while there is a high possibility of further places to suffer such exposures in the near future. METHODS: We employed bioengineered 3D human liver and cardiac organoids to screen a panel of environmental toxins (lead, mercury, thallium, and glyphosate), and charted the response of the organoids to these compounds. Liver and cardiac organoids were exposed to lead (10 µM–10 mM), mercury (200 nM–200 µM), thallium (10 nM–10 µM), or glyphosate (25 µM–25 mM) for a duration of 48 h. The impacts of toxin exposure were then assessed by LIVE/DEAD viability and cytotoxicity staining, measuring ATP activity and determining IC50 values, and determining changes in cardiac organoid beating activity. RESULTS: As expected, all of the toxins induced toxicity in the organoids. Both ATP and LIVE/DEAD assays showed toxicity in both liver and cardiac organoids. In particular, thallium was the most toxic, with IC50 values of 13.5 and 1.35 µM in liver and cardiac organoids, respectively. Conversely, glyphosate was the least toxic of the four compounds, with IC50 values of 10.53 and 10.85 mM in liver and cardiac organoids, respectively. Additionally, toxins had a negative influence on cardiac organoid beating activity as well. Thallium resulting in the most significant decreases in beating rate, followed by mercury, then glyphosate, and finally, lead. These results suggest that the 3D organoids have significant utility to be deployed in additional toxicity screening applications, and future development of treatments to mitigate exposures. CONCLUSION: 3D organoids have significant utility to be deployed in additional toxicity screening applications, such as future development of treatments to mitigate exposures, drug screening, and environmental toxin detection. Frontiers Media S.A. 2018-04-16 /pmc/articles/PMC5932352/ /pubmed/29755963 http://dx.doi.org/10.3389/fpubh.2018.00103 Text en Copyright © 2018 Forsythe, Devarasetty, Shupe, Bishop, Atala, Soker and Skardal. 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 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 Public Health
Forsythe, Steven D.
Devarasetty, Mahesh
Shupe, Thomas
Bishop, Colin
Atala, Anthony
Soker, Shay
Skardal, Aleksander
Environmental Toxin Screening Using Human-Derived 3D Bioengineered Liver and Cardiac Organoids
title Environmental Toxin Screening Using Human-Derived 3D Bioengineered Liver and Cardiac Organoids
title_full Environmental Toxin Screening Using Human-Derived 3D Bioengineered Liver and Cardiac Organoids
title_fullStr Environmental Toxin Screening Using Human-Derived 3D Bioengineered Liver and Cardiac Organoids
title_full_unstemmed Environmental Toxin Screening Using Human-Derived 3D Bioengineered Liver and Cardiac Organoids
title_short Environmental Toxin Screening Using Human-Derived 3D Bioengineered Liver and Cardiac Organoids
title_sort environmental toxin screening using human-derived 3d bioengineered liver and cardiac organoids
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5932352/
https://www.ncbi.nlm.nih.gov/pubmed/29755963
http://dx.doi.org/10.3389/fpubh.2018.00103
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