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Investigating the applicability domain of the hiPSC-based PluriLum assay: an embryotoxicity assessment of chemicals and drugs
To meet the growing demand for developmental toxicity assessment of chemicals, New Approach Methodologies (NAMs) are needed. Previously, we developed two 3D in vitro assays based on human-induced pluripotent stem cells (hiPSC) and cardiomyocyte differentiation: the PluriBeat assay, based on assessme...
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Published in: | Archives of toxicology 2024-04, Vol.98 (4), p.1209-1224 |
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description | To meet the growing demand for developmental toxicity assessment of chemicals, New Approach Methodologies (NAMs) are needed. Previously, we developed two 3D in vitro assays based on human-induced pluripotent stem cells (hiPSC) and cardiomyocyte differentiation: the PluriBeat assay, based on assessment of beating differentiated embryoid bodies, and the PluriLum assay, a reporter gene assay based on the expression of the early cardiac marker
NKX2.5
; both promising assays for predicting embryotoxic effects of chemicals and drugs. In this work, we aimed to further describe the predictive power of the PluriLum assay and compare its sensitivity with PluriBeat and similar human stem cell-based assays developed by others. For this purpose, we assessed the toxicity of a panel of ten chemicals from different chemical classes, consisting of the known developmental toxicants 5-fluorouracil, all-
trans
retinoic acid and valproic acid, as well as the negative control compounds ascorbic acid and folic acid. In addition, the fungicides epoxiconazole and prochloraz, and three perfluoroalkyl substances (PFAS), PFOS, PFOA and GenX were tested. Generally, the PluriLum assay displayed higher sensitivity when compared to the PluriBeat assay. For several compounds the luminescence readout of the PluriLum assay showed effects not detected by the PluriBeat assay, including two PFAS compounds and the two fungicides. Overall, we find that the PluriLum assay has the potential to provide a fast and objective detection of developmental toxicants and has a level of sensitivity that is comparable to or higher than other in vitro assays also based on human stem cells and cardiomyocyte differentiation for assessment of developmental toxicity. |
doi_str_mv | 10.1007/s00204-023-03675-1 |
format | article |
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NKX2.5
; both promising assays for predicting embryotoxic effects of chemicals and drugs. In this work, we aimed to further describe the predictive power of the PluriLum assay and compare its sensitivity with PluriBeat and similar human stem cell-based assays developed by others. For this purpose, we assessed the toxicity of a panel of ten chemicals from different chemical classes, consisting of the known developmental toxicants 5-fluorouracil, all-
trans
retinoic acid and valproic acid, as well as the negative control compounds ascorbic acid and folic acid. In addition, the fungicides epoxiconazole and prochloraz, and three perfluoroalkyl substances (PFAS), PFOS, PFOA and GenX were tested. Generally, the PluriLum assay displayed higher sensitivity when compared to the PluriBeat assay. For several compounds the luminescence readout of the PluriLum assay showed effects not detected by the PluriBeat assay, including two PFAS compounds and the two fungicides. Overall, we find that the PluriLum assay has the potential to provide a fast and objective detection of developmental toxicants and has a level of sensitivity that is comparable to or higher than other in vitro assays also based on human stem cells and cardiomyocyte differentiation for assessment of developmental toxicity.</description><identifier>ISSN: 0340-5761</identifier><identifier>ISSN: 1432-0738</identifier><identifier>EISSN: 1432-0738</identifier><identifier>DOI: 10.1007/s00204-023-03675-1</identifier><identifier>PMID: 38311648</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>5-Fluorouracil ; Acids ; Ascorbic acid ; Assaying ; Biomedical and Life Sciences ; Biomedicine ; Cardiomyocytes ; Cell Differentiation ; Chemicals ; Contaminants ; Differentiation ; domain ; Drugs ; Embryoid Bodies ; embryotoxicity ; Environmental Health ; Epoxiconazole ; Fluorocarbons ; fluorouracil ; Folic acid ; Fungicides ; Fungicides, Industrial ; Hazardous Substances ; Human influences ; Humans ; Induced Pluripotent Stem Cells ; luminescence ; Nkx2.5 protein ; Occupational Medicine/Industrial Medicine ; Perfluoroalkyl & polyfluoroalkyl substances ; perfluorocarbons ; Perfluorochemicals ; Perfluorooctane sulfonic acid ; Perfluorooctanoic acid ; Pesticides ; Pharmacology/Toxicology ; Pluripotency ; Prochloraz ; Reporter gene ; reporter genes ; Reproductive Toxicology ; Retinoic acid ; Sensitivity ; Stem cells ; Toxicants ; Toxicity ; Toxicity Tests - methods ; Valproic acid</subject><ispartof>Archives of toxicology, 2024-04, Vol.98 (4), p.1209-1224</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c459t-77b7c7d0bb74a47ebb6f890d50b51f2e03b1cb8eb5c2432ceb2e785e5e56c5913</cites><orcidid>0000-0002-0545-7857</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38311648$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Treschow, Andreas Frederik</creatorcontrib><creatorcontrib>Valente, Maria João</creatorcontrib><creatorcontrib>Lauschke, Karin</creatorcontrib><creatorcontrib>Holst, Bjørn</creatorcontrib><creatorcontrib>Andersen, Anders Reenberg</creatorcontrib><creatorcontrib>Vinggaard, Anne Marie</creatorcontrib><title>Investigating the applicability domain of the hiPSC-based PluriLum assay: an embryotoxicity assessment of chemicals and drugs</title><title>Archives of toxicology</title><addtitle>Arch Toxicol</addtitle><addtitle>Arch Toxicol</addtitle><description>To meet the growing demand for developmental toxicity assessment of chemicals, New Approach Methodologies (NAMs) are needed. Previously, we developed two 3D in vitro assays based on human-induced pluripotent stem cells (hiPSC) and cardiomyocyte differentiation: the PluriBeat assay, based on assessment of beating differentiated embryoid bodies, and the PluriLum assay, a reporter gene assay based on the expression of the early cardiac marker
NKX2.5
; both promising assays for predicting embryotoxic effects of chemicals and drugs. In this work, we aimed to further describe the predictive power of the PluriLum assay and compare its sensitivity with PluriBeat and similar human stem cell-based assays developed by others. For this purpose, we assessed the toxicity of a panel of ten chemicals from different chemical classes, consisting of the known developmental toxicants 5-fluorouracil, all-
trans
retinoic acid and valproic acid, as well as the negative control compounds ascorbic acid and folic acid. In addition, the fungicides epoxiconazole and prochloraz, and three perfluoroalkyl substances (PFAS), PFOS, PFOA and GenX were tested. Generally, the PluriLum assay displayed higher sensitivity when compared to the PluriBeat assay. For several compounds the luminescence readout of the PluriLum assay showed effects not detected by the PluriBeat assay, including two PFAS compounds and the two fungicides. Overall, we find that the PluriLum assay has the potential to provide a fast and objective detection of developmental toxicants and has a level of sensitivity that is comparable to or higher than other in vitro assays also based on human stem cells and cardiomyocyte differentiation for assessment of developmental toxicity.</description><subject>5-Fluorouracil</subject><subject>Acids</subject><subject>Ascorbic acid</subject><subject>Assaying</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cardiomyocytes</subject><subject>Cell Differentiation</subject><subject>Chemicals</subject><subject>Contaminants</subject><subject>Differentiation</subject><subject>domain</subject><subject>Drugs</subject><subject>Embryoid Bodies</subject><subject>embryotoxicity</subject><subject>Environmental Health</subject><subject>Epoxiconazole</subject><subject>Fluorocarbons</subject><subject>fluorouracil</subject><subject>Folic acid</subject><subject>Fungicides</subject><subject>Fungicides, Industrial</subject><subject>Hazardous Substances</subject><subject>Human influences</subject><subject>Humans</subject><subject>Induced Pluripotent Stem Cells</subject><subject>luminescence</subject><subject>Nkx2.5 protein</subject><subject>Occupational Medicine/Industrial Medicine</subject><subject>Perfluoroalkyl & polyfluoroalkyl substances</subject><subject>perfluorocarbons</subject><subject>Perfluorochemicals</subject><subject>Perfluorooctane sulfonic acid</subject><subject>Perfluorooctanoic acid</subject><subject>Pesticides</subject><subject>Pharmacology/Toxicology</subject><subject>Pluripotency</subject><subject>Prochloraz</subject><subject>Reporter gene</subject><subject>reporter genes</subject><subject>Reproductive Toxicology</subject><subject>Retinoic acid</subject><subject>Sensitivity</subject><subject>Stem cells</subject><subject>Toxicants</subject><subject>Toxicity</subject><subject>Toxicity Tests - methods</subject><subject>Valproic acid</subject><issn>0340-5761</issn><issn>1432-0738</issn><issn>1432-0738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kstu1DAUhi0EokPhBVigSGzYBI5vccIGVSMulUaiErC2bOdkxlUSD3ZSMQveHWemlMui8sKS_-_85-JDyHMKrymAepMAGIgSGC-BV0qW9AFZUcFZCYrXD8kKuIBSqoqekScpXQNQVjf8MTnjNae0EvWK_LwcbzBNfmsmP26LaYeF2e9774z1vZ8ORRsG48cidEdt56--rEtrErbFVT9Hv5mHwqRkDm8LMxY42HgIU_jh3RKbBUxpwHFa4t0Oh-zbp0y2RRvnbXpKHnX5AZ_d3ufk24f3X9efys3nj5fri03phGymUimrnGrBWiWMUGht1dUNtBKspB1D4JY6W6OVjuX2HVqGqpaYT-VkQ_k5eXfy3c92wNbliqLp9T76wcSDDsbrf5XR7_Q23GgKjRCCyezw6tYhhu9znpgefHLY92bEMCfNqeQ1SHZMdj_KGsaEBKUW15f_oddhjmMeRaakqvP_Vk2m2IlyMaQUsbsrnIJeNkGfNkHnTdDHTdBLFS_-bvku5PfXZ4CfgJSlcYvxT-57bH8BzEjA4w</recordid><startdate>20240401</startdate><enddate>20240401</enddate><creator>Treschow, Andreas Frederik</creator><creator>Valente, Maria João</creator><creator>Lauschke, Karin</creator><creator>Holst, Bjørn</creator><creator>Andersen, Anders Reenberg</creator><creator>Vinggaard, Anne Marie</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T2</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>K9.</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0545-7857</orcidid></search><sort><creationdate>20240401</creationdate><title>Investigating the applicability domain of the hiPSC-based PluriLum assay: an embryotoxicity assessment of chemicals and drugs</title><author>Treschow, Andreas Frederik ; 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Previously, we developed two 3D in vitro assays based on human-induced pluripotent stem cells (hiPSC) and cardiomyocyte differentiation: the PluriBeat assay, based on assessment of beating differentiated embryoid bodies, and the PluriLum assay, a reporter gene assay based on the expression of the early cardiac marker
NKX2.5
; both promising assays for predicting embryotoxic effects of chemicals and drugs. In this work, we aimed to further describe the predictive power of the PluriLum assay and compare its sensitivity with PluriBeat and similar human stem cell-based assays developed by others. For this purpose, we assessed the toxicity of a panel of ten chemicals from different chemical classes, consisting of the known developmental toxicants 5-fluorouracil, all-
trans
retinoic acid and valproic acid, as well as the negative control compounds ascorbic acid and folic acid. In addition, the fungicides epoxiconazole and prochloraz, and three perfluoroalkyl substances (PFAS), PFOS, PFOA and GenX were tested. Generally, the PluriLum assay displayed higher sensitivity when compared to the PluriBeat assay. For several compounds the luminescence readout of the PluriLum assay showed effects not detected by the PluriBeat assay, including two PFAS compounds and the two fungicides. Overall, we find that the PluriLum assay has the potential to provide a fast and objective detection of developmental toxicants and has a level of sensitivity that is comparable to or higher than other in vitro assays also based on human stem cells and cardiomyocyte differentiation for assessment of developmental toxicity.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>38311648</pmid><doi>10.1007/s00204-023-03675-1</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-0545-7857</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 5-Fluorouracil Acids Ascorbic acid Assaying Biomedical and Life Sciences Biomedicine Cardiomyocytes Cell Differentiation Chemicals Contaminants Differentiation domain Drugs Embryoid Bodies embryotoxicity Environmental Health Epoxiconazole Fluorocarbons fluorouracil Folic acid Fungicides Fungicides, Industrial Hazardous Substances Human influences Humans Induced Pluripotent Stem Cells luminescence Nkx2.5 protein Occupational Medicine/Industrial Medicine Perfluoroalkyl & polyfluoroalkyl substances perfluorocarbons Perfluorochemicals Perfluorooctane sulfonic acid Perfluorooctanoic acid Pesticides Pharmacology/Toxicology Pluripotency Prochloraz Reporter gene reporter genes Reproductive Toxicology Retinoic acid Sensitivity Stem cells Toxicants Toxicity Toxicity Tests - methods Valproic acid |
title | Investigating the applicability domain of the hiPSC-based PluriLum assay: an embryotoxicity assessment of chemicals and drugs |
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