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Different responses of Caco-2 and MCF-7 cells to silver nanoparticles are based on highly similar mechanisms of action
The mode of action of silver nanoparticles (AgNPs) is suggested to be exerted through both Ag + and AgNP dependent mechanisms. Ingestion is one of the major NP exposure routes, and potential effects are often studied using Caco-2 cells, a well-established model for the gut epithelium. MCF-7 cells ar...
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Published in: | Nanotoxicology 2016-12, Vol.10 (10), p.1431-1441 |
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creator | van der Zande, Meike Undas, Anna K. Kramer, Evelien Monopoli, Marco P. Peters, Ruud J. Garry, David Antunes Fernandes, Elsa C. Hendriksen, Peter J. Marvin, Hans J.P. Peijnenburg, Ad A. Bouwmeester, Hans |
description | The mode of action of silver nanoparticles (AgNPs) is suggested to be exerted through both Ag
+
and AgNP dependent mechanisms. Ingestion is one of the major NP exposure routes, and potential effects are often studied using Caco-2 cells, a well-established model for the gut epithelium. MCF-7 cells are epithelial breast cancer cells with extensive well-characterized toxicogenomics profiles. In the present study, we aimed to gain a deeper understanding of the cellular molecular responses in Caco-2 and MCF-7 cells after AgNP exposure in order to evaluate whether epithelial cells derived from different tissues demonstrated similar responses. These insights could possibly reduce the size of cell panels for NP hazard identification screening purposes. AgNPs of 20, 30, 60, and 110 nm, and AgNO
3
were exposed for 6 h and 24 h. AgNPs were shown to be taken up and dissolve intracellularly. Compared with MCF-7 cells, Caco-2 cells showed a higher sensitivity to AgNPs, slower gene expression kinetics and absence of NP size-dependent responses. However, on a molecular level, no significant differences were observed between the two cell types. Transcriptomic analysis showed that Ag(NP) exposure caused (oxidative) stress responses, possibly leading to cell death in both cell lines. There was no indication for effects specifically induced by AgNPs. Responses to AgNPs appeared to be induced by silver ions released from the AgNPs. In conclusion, differences in mRNA responses to AgNPs between Caco-2 and MCF-7 cells were mainly related to timing and magnitude, but not to a different underlying mechanism. |
doi_str_mv | 10.1080/17435390.2016.1225132 |
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+
and AgNP dependent mechanisms. Ingestion is one of the major NP exposure routes, and potential effects are often studied using Caco-2 cells, a well-established model for the gut epithelium. MCF-7 cells are epithelial breast cancer cells with extensive well-characterized toxicogenomics profiles. In the present study, we aimed to gain a deeper understanding of the cellular molecular responses in Caco-2 and MCF-7 cells after AgNP exposure in order to evaluate whether epithelial cells derived from different tissues demonstrated similar responses. These insights could possibly reduce the size of cell panels for NP hazard identification screening purposes. AgNPs of 20, 30, 60, and 110 nm, and AgNO
3
were exposed for 6 h and 24 h. AgNPs were shown to be taken up and dissolve intracellularly. Compared with MCF-7 cells, Caco-2 cells showed a higher sensitivity to AgNPs, slower gene expression kinetics and absence of NP size-dependent responses. However, on a molecular level, no significant differences were observed between the two cell types. Transcriptomic analysis showed that Ag(NP) exposure caused (oxidative) stress responses, possibly leading to cell death in both cell lines. There was no indication for effects specifically induced by AgNPs. Responses to AgNPs appeared to be induced by silver ions released from the AgNPs. In conclusion, differences in mRNA responses to AgNPs between Caco-2 and MCF-7 cells were mainly related to timing and magnitude, but not to a different underlying mechanism.</description><identifier>ISSN: 1743-5390</identifier><identifier>EISSN: 1743-5404</identifier><identifier>DOI: 10.1080/17435390.2016.1225132</identifier><identifier>PMID: 27597447</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>Caco-2 ; Caco-2 Cells ; Cell Culture Techniques ; Cell Survival - drug effects ; Dose-Response Relationship, Drug ; Epithelial Cells - drug effects ; Gene expression ; Gene Expression Profiling ; Humans ; in vitro ; Kinetics ; MCF-7 ; MCF-7 Cells ; Metal Nanoparticles - toxicity ; Nanoparticles ; Oxidative Stress - drug effects ; Particle Size ; Silver ; Silver - metabolism ; Silver - toxicity ; silver nanoparticles ; Silver Nitrate - toxicity ; Surface Properties ; toxicogenomics ; Transcriptome - drug effects</subject><ispartof>Nanotoxicology, 2016-12, Vol.10 (10), p.1431-1441</ispartof><rights>2016 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2016</rights><rights>2016 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.</rights><rights>Wageningen University & Research</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c525t-2d99145e877e7cb793f9a8246dbf0e8924399ec08201d8a7b4f170356835edf63</citedby><cites>FETCH-LOGICAL-c525t-2d99145e877e7cb793f9a8246dbf0e8924399ec08201d8a7b4f170356835edf63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27597447$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van der Zande, Meike</creatorcontrib><creatorcontrib>Undas, Anna K.</creatorcontrib><creatorcontrib>Kramer, Evelien</creatorcontrib><creatorcontrib>Monopoli, Marco P.</creatorcontrib><creatorcontrib>Peters, Ruud J.</creatorcontrib><creatorcontrib>Garry, David</creatorcontrib><creatorcontrib>Antunes Fernandes, Elsa C.</creatorcontrib><creatorcontrib>Hendriksen, Peter J.</creatorcontrib><creatorcontrib>Marvin, Hans J.P.</creatorcontrib><creatorcontrib>Peijnenburg, Ad A.</creatorcontrib><creatorcontrib>Bouwmeester, Hans</creatorcontrib><title>Different responses of Caco-2 and MCF-7 cells to silver nanoparticles are based on highly similar mechanisms of action</title><title>Nanotoxicology</title><addtitle>Nanotoxicology</addtitle><description>The mode of action of silver nanoparticles (AgNPs) is suggested to be exerted through both Ag
+
and AgNP dependent mechanisms. Ingestion is one of the major NP exposure routes, and potential effects are often studied using Caco-2 cells, a well-established model for the gut epithelium. MCF-7 cells are epithelial breast cancer cells with extensive well-characterized toxicogenomics profiles. In the present study, we aimed to gain a deeper understanding of the cellular molecular responses in Caco-2 and MCF-7 cells after AgNP exposure in order to evaluate whether epithelial cells derived from different tissues demonstrated similar responses. These insights could possibly reduce the size of cell panels for NP hazard identification screening purposes. AgNPs of 20, 30, 60, and 110 nm, and AgNO
3
were exposed for 6 h and 24 h. AgNPs were shown to be taken up and dissolve intracellularly. Compared with MCF-7 cells, Caco-2 cells showed a higher sensitivity to AgNPs, slower gene expression kinetics and absence of NP size-dependent responses. However, on a molecular level, no significant differences were observed between the two cell types. Transcriptomic analysis showed that Ag(NP) exposure caused (oxidative) stress responses, possibly leading to cell death in both cell lines. There was no indication for effects specifically induced by AgNPs. Responses to AgNPs appeared to be induced by silver ions released from the AgNPs. In conclusion, differences in mRNA responses to AgNPs between Caco-2 and MCF-7 cells were mainly related to timing and magnitude, but not to a different underlying mechanism.</description><subject>Caco-2</subject><subject>Caco-2 Cells</subject><subject>Cell Culture Techniques</subject><subject>Cell Survival - drug effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Epithelial Cells - drug effects</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Humans</subject><subject>in vitro</subject><subject>Kinetics</subject><subject>MCF-7</subject><subject>MCF-7 Cells</subject><subject>Metal Nanoparticles - toxicity</subject><subject>Nanoparticles</subject><subject>Oxidative Stress - drug effects</subject><subject>Particle Size</subject><subject>Silver</subject><subject>Silver - metabolism</subject><subject>Silver - toxicity</subject><subject>silver nanoparticles</subject><subject>Silver Nitrate - toxicity</subject><subject>Surface Properties</subject><subject>toxicogenomics</subject><subject>Transcriptome - drug effects</subject><issn>1743-5390</issn><issn>1743-5404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><recordid>eNp9kU-PFCEQxTtG4_7Rj6Ah8eKlR6ChaTxpRldN1njRM6HpYocNDS1072S-vfTOjAcPXihCfu8VVa-qXhG8IbjD74hgDW8k3lBM2g2hlJOGPqku1_eaM8yenu8Fuqiucr7HmLe0Jc-rCyq4FIyJy-rhk7MWEoQZJchTDBkyihZttYk1RToM6Pv2phbIgPcZzRFl5x8goaBDnHSanfFFoROgXmcYUAxo5-52_lDA0Xmd0Ahmp4PL46OxNrOL4UX1zGqf4eWpXle_bj7_3H6tb398-bb9eFsbTvlc00FKwjh0QoAwvZCNlbqjrB16i6GTlDVSgsFdWcLQadEzSwRueNs1HAbbNtfV-6PvXt9BcKEcKuhkXFZRO-Vdn3Q6qP2SVPBrmZY-K45FK2kRvz2KpxR_L5BnNbq87kEHiEtWRGIiCitZQd_8g97HJYUymiJdKzgvUYhC8SNlUsw5gVVTcuP6AYLVmqo6p6rWVNUp1aJ7fXJf-hGGv6pzjAX4cARcsDGNeh-TH9SsDz4mm3RY523-3-MPX7exTw</recordid><startdate>20161201</startdate><enddate>20161201</enddate><creator>van der Zande, Meike</creator><creator>Undas, Anna K.</creator><creator>Kramer, Evelien</creator><creator>Monopoli, Marco P.</creator><creator>Peters, Ruud J.</creator><creator>Garry, David</creator><creator>Antunes Fernandes, Elsa C.</creator><creator>Hendriksen, Peter J.</creator><creator>Marvin, Hans J.P.</creator><creator>Peijnenburg, Ad A.</creator><creator>Bouwmeester, Hans</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><scope>0YH</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>7U7</scope><scope>C1K</scope><scope>QVL</scope></search><sort><creationdate>20161201</creationdate><title>Different responses of Caco-2 and MCF-7 cells to silver nanoparticles are based on highly similar mechanisms of action</title><author>van der Zande, Meike ; Undas, Anna K. ; Kramer, Evelien ; Monopoli, Marco P. ; Peters, Ruud J. ; Garry, David ; Antunes Fernandes, Elsa C. ; Hendriksen, Peter J. ; Marvin, Hans J.P. ; Peijnenburg, Ad A. ; Bouwmeester, Hans</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c525t-2d99145e877e7cb793f9a8246dbf0e8924399ec08201d8a7b4f170356835edf63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Caco-2</topic><topic>Caco-2 Cells</topic><topic>Cell Culture Techniques</topic><topic>Cell Survival - drug effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Epithelial Cells - drug effects</topic><topic>Gene expression</topic><topic>Gene Expression Profiling</topic><topic>Humans</topic><topic>in vitro</topic><topic>Kinetics</topic><topic>MCF-7</topic><topic>MCF-7 Cells</topic><topic>Metal Nanoparticles - toxicity</topic><topic>Nanoparticles</topic><topic>Oxidative Stress - drug effects</topic><topic>Particle Size</topic><topic>Silver</topic><topic>Silver - metabolism</topic><topic>Silver - toxicity</topic><topic>silver nanoparticles</topic><topic>Silver Nitrate - toxicity</topic><topic>Surface Properties</topic><topic>toxicogenomics</topic><topic>Transcriptome - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van der Zande, Meike</creatorcontrib><creatorcontrib>Undas, Anna K.</creatorcontrib><creatorcontrib>Kramer, Evelien</creatorcontrib><creatorcontrib>Monopoli, Marco P.</creatorcontrib><creatorcontrib>Peters, Ruud J.</creatorcontrib><creatorcontrib>Garry, David</creatorcontrib><creatorcontrib>Antunes Fernandes, Elsa C.</creatorcontrib><creatorcontrib>Hendriksen, Peter J.</creatorcontrib><creatorcontrib>Marvin, Hans J.P.</creatorcontrib><creatorcontrib>Peijnenburg, Ad A.</creatorcontrib><creatorcontrib>Bouwmeester, Hans</creatorcontrib><collection>Taylor & Francis Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>NARCIS:Publications</collection><jtitle>Nanotoxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van der Zande, Meike</au><au>Undas, Anna K.</au><au>Kramer, Evelien</au><au>Monopoli, Marco P.</au><au>Peters, Ruud J.</au><au>Garry, David</au><au>Antunes Fernandes, Elsa C.</au><au>Hendriksen, Peter J.</au><au>Marvin, Hans J.P.</au><au>Peijnenburg, Ad A.</au><au>Bouwmeester, Hans</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Different responses of Caco-2 and MCF-7 cells to silver nanoparticles are based on highly similar mechanisms of action</atitle><jtitle>Nanotoxicology</jtitle><addtitle>Nanotoxicology</addtitle><date>2016-12-01</date><risdate>2016</risdate><volume>10</volume><issue>10</issue><spage>1431</spage><epage>1441</epage><pages>1431-1441</pages><issn>1743-5390</issn><eissn>1743-5404</eissn><abstract>The mode of action of silver nanoparticles (AgNPs) is suggested to be exerted through both Ag
+
and AgNP dependent mechanisms. Ingestion is one of the major NP exposure routes, and potential effects are often studied using Caco-2 cells, a well-established model for the gut epithelium. MCF-7 cells are epithelial breast cancer cells with extensive well-characterized toxicogenomics profiles. In the present study, we aimed to gain a deeper understanding of the cellular molecular responses in Caco-2 and MCF-7 cells after AgNP exposure in order to evaluate whether epithelial cells derived from different tissues demonstrated similar responses. These insights could possibly reduce the size of cell panels for NP hazard identification screening purposes. AgNPs of 20, 30, 60, and 110 nm, and AgNO
3
were exposed for 6 h and 24 h. AgNPs were shown to be taken up and dissolve intracellularly. Compared with MCF-7 cells, Caco-2 cells showed a higher sensitivity to AgNPs, slower gene expression kinetics and absence of NP size-dependent responses. However, on a molecular level, no significant differences were observed between the two cell types. Transcriptomic analysis showed that Ag(NP) exposure caused (oxidative) stress responses, possibly leading to cell death in both cell lines. There was no indication for effects specifically induced by AgNPs. Responses to AgNPs appeared to be induced by silver ions released from the AgNPs. In conclusion, differences in mRNA responses to AgNPs between Caco-2 and MCF-7 cells were mainly related to timing and magnitude, but not to a different underlying mechanism.</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>27597447</pmid><doi>10.1080/17435390.2016.1225132</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Caco-2 Caco-2 Cells Cell Culture Techniques Cell Survival - drug effects Dose-Response Relationship, Drug Epithelial Cells - drug effects Gene expression Gene Expression Profiling Humans in vitro Kinetics MCF-7 MCF-7 Cells Metal Nanoparticles - toxicity Nanoparticles Oxidative Stress - drug effects Particle Size Silver Silver - metabolism Silver - toxicity silver nanoparticles Silver Nitrate - toxicity Surface Properties toxicogenomics Transcriptome - drug effects |
title | Different responses of Caco-2 and MCF-7 cells to silver nanoparticles are based on highly similar mechanisms of action |
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