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Early Warnings by Liver Organoids on Short- and Long-Chain PFAS Toxicity

Short-chain per-fluoroalkyl substances (PFAS) have replaced long-chains in many applications, however the toxicity and its mode of action and interactions due to the large number of these compounds and their mixtures is still poorly understood. The paper aims to compare the effects on mouse liver or...

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Autores principales: Palazzolo, Stefano, Caligiuri, Isabella, Sfriso, Andrea Augusto, Mauceri, Matteo, Rotondo, Rossella, Campagnol, Davide, Canzonieri, Vincenzo, Rizzolio, Flavio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879043/
https://www.ncbi.nlm.nih.gov/pubmed/35202277
http://dx.doi.org/10.3390/toxics10020091
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author Palazzolo, Stefano
Caligiuri, Isabella
Sfriso, Andrea Augusto
Mauceri, Matteo
Rotondo, Rossella
Campagnol, Davide
Canzonieri, Vincenzo
Rizzolio, Flavio
author_facet Palazzolo, Stefano
Caligiuri, Isabella
Sfriso, Andrea Augusto
Mauceri, Matteo
Rotondo, Rossella
Campagnol, Davide
Canzonieri, Vincenzo
Rizzolio, Flavio
author_sort Palazzolo, Stefano
collection PubMed
description Short-chain per-fluoroalkyl substances (PFAS) have replaced long-chains in many applications, however the toxicity and its mode of action and interactions due to the large number of these compounds and their mixtures is still poorly understood. The paper aims to compare the effects on mouse liver organoids (target organ for bioaccumulation) of two long-chain PFAS (perfluorooctane sulfonate -PFOS-, perfluorooctanoic acid -PFOA) and two short-chain PFAS commonly utilized in the industry (heptafluorobutyric acid -HFBA-, Pentafluoropropionic anhydride-PFPA) to identify the mode of action of these classes of contaminants. Cytomorphological aberrations and ALT/GDH enzyme disruption were identified but no acute toxicity endpoint neither apoptosis was detected by the two tested short-chain PFAS. After cytomorphological analysis, it is evident that short-chain PFAS affected organoid morphology inducing a reduction of cytostructural complexity and aberrant cytological features. Conversely, EC50 values of 670 ± 30 µM and 895 ± 7 µM were measured for PFOS and PFOA, respectively, together with strong ALT/GDH enzyme disruption, caspase 3 and 7 apoptosis activation and deep loss of architectural complexity of organoids in the range of 500–1000 µM. Eventually, biochemical markers and histology analysis confirmed the sensitivity of organoid tests that could be used as a fast and reproducible platform to test many PFAS and mixtures saving time and at low cost in comparison with in vivo tests. Organoids testing could be introduced as an innovative platform to assess the toxicity to fast recognize potentially dangerous pollutants.
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spelling pubmed-88790432022-02-26 Early Warnings by Liver Organoids on Short- and Long-Chain PFAS Toxicity Palazzolo, Stefano Caligiuri, Isabella Sfriso, Andrea Augusto Mauceri, Matteo Rotondo, Rossella Campagnol, Davide Canzonieri, Vincenzo Rizzolio, Flavio Toxics Article Short-chain per-fluoroalkyl substances (PFAS) have replaced long-chains in many applications, however the toxicity and its mode of action and interactions due to the large number of these compounds and their mixtures is still poorly understood. The paper aims to compare the effects on mouse liver organoids (target organ for bioaccumulation) of two long-chain PFAS (perfluorooctane sulfonate -PFOS-, perfluorooctanoic acid -PFOA) and two short-chain PFAS commonly utilized in the industry (heptafluorobutyric acid -HFBA-, Pentafluoropropionic anhydride-PFPA) to identify the mode of action of these classes of contaminants. Cytomorphological aberrations and ALT/GDH enzyme disruption were identified but no acute toxicity endpoint neither apoptosis was detected by the two tested short-chain PFAS. After cytomorphological analysis, it is evident that short-chain PFAS affected organoid morphology inducing a reduction of cytostructural complexity and aberrant cytological features. Conversely, EC50 values of 670 ± 30 µM and 895 ± 7 µM were measured for PFOS and PFOA, respectively, together with strong ALT/GDH enzyme disruption, caspase 3 and 7 apoptosis activation and deep loss of architectural complexity of organoids in the range of 500–1000 µM. Eventually, biochemical markers and histology analysis confirmed the sensitivity of organoid tests that could be used as a fast and reproducible platform to test many PFAS and mixtures saving time and at low cost in comparison with in vivo tests. Organoids testing could be introduced as an innovative platform to assess the toxicity to fast recognize potentially dangerous pollutants. MDPI 2022-02-18 /pmc/articles/PMC8879043/ /pubmed/35202277 http://dx.doi.org/10.3390/toxics10020091 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Palazzolo, Stefano
Caligiuri, Isabella
Sfriso, Andrea Augusto
Mauceri, Matteo
Rotondo, Rossella
Campagnol, Davide
Canzonieri, Vincenzo
Rizzolio, Flavio
Early Warnings by Liver Organoids on Short- and Long-Chain PFAS Toxicity
title Early Warnings by Liver Organoids on Short- and Long-Chain PFAS Toxicity
title_full Early Warnings by Liver Organoids on Short- and Long-Chain PFAS Toxicity
title_fullStr Early Warnings by Liver Organoids on Short- and Long-Chain PFAS Toxicity
title_full_unstemmed Early Warnings by Liver Organoids on Short- and Long-Chain PFAS Toxicity
title_short Early Warnings by Liver Organoids on Short- and Long-Chain PFAS Toxicity
title_sort early warnings by liver organoids on short- and long-chain pfas toxicity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879043/
https://www.ncbi.nlm.nih.gov/pubmed/35202277
http://dx.doi.org/10.3390/toxics10020091
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