Differential effects of graphene materials on the metabolism and function of human skin cells
Graphene-related materials (GRMs) such as graphene oxide (GO) and few-layer graphene (FLG) are used in multiple biomedical applications; however, there is still insufficient information available regarding their interactions with the main biological barriers such as skin. In this study, we explored...
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Veröffentlicht in: | Nanoscale 2018-06, Vol.10 (24), p.11604-11615 |
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description | Graphene-related materials (GRMs) such as graphene oxide (GO) and few-layer graphene (FLG) are used in multiple biomedical applications; however, there is still insufficient information available regarding their interactions with the main biological barriers such as skin. In this study, we explored the effects of GO and FLG on HaCaTs human skin keratinocytes, using NMR-based metabolomics and fluorescence microscopy to evaluate the global impact of each GRM on cell fate and damage. GO and FLG at low concentrations (5 μg mL-1) induced a differential remodeling of the metabolome, preceded by an increase in the level of radical oxygen species (ROS) and free cytosolic Ca2+. These changes are linked to a concentration-dependent increase in cell death by triggering apoptosis and necrosis, the latter being predominant at higher concentrations of the nanostructures. In addition, both compounds reduce the ability of HaCaT cells to heal wounds. Our results demonstrate that the GO and FLG used in this study, which mainly differ in their oxidation state, slightly trigger differential effects on HaCaTs cells, but with evident outcomes at the cellular and molecular levels. Their behavior as pro-apoptotic/necrotic substances and their ability to inhibit cell migration, even at low doses, should be considered in the development of future applications. |
doi_str_mv | 10.1039/c8nr00897c |
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In this study, we explored the effects of GO and FLG on HaCaTs human skin keratinocytes, using NMR-based metabolomics and fluorescence microscopy to evaluate the global impact of each GRM on cell fate and damage. GO and FLG at low concentrations (5 μg mL-1) induced a differential remodeling of the metabolome, preceded by an increase in the level of radical oxygen species (ROS) and free cytosolic Ca2+. These changes are linked to a concentration-dependent increase in cell death by triggering apoptosis and necrosis, the latter being predominant at higher concentrations of the nanostructures. In addition, both compounds reduce the ability of HaCaT cells to heal wounds. Our results demonstrate that the GO and FLG used in this study, which mainly differ in their oxidation state, slightly trigger differential effects on HaCaTs cells, but with evident outcomes at the cellular and molecular levels. Their behavior as pro-apoptotic/necrotic substances and their ability to inhibit cell migration, even at low doses, should be considered in the development of future applications.</description><identifier>ISSN: 2040-3364</identifier><identifier>EISSN: 2040-3372</identifier><identifier>DOI: 10.1039/c8nr00897c</identifier><identifier>PMID: 29892760</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Apoptosis ; Biomedical materials ; Calcium ions ; Cell adhesion & migration ; Cell death ; Cell Line ; Fluorescence ; Graphene ; Graphite - pharmacology ; Humans ; Impact damage ; Keratinocytes - drug effects ; Low concentrations ; Metabolism ; Molecular chains ; Nanostructures ; Necrosis ; NMR ; Nuclear magnetic resonance ; Oxidation ; Oxides ; Reactive Oxygen Species ; Skin ; Skin - cytology ; Skin - drug effects ; Valence</subject><ispartof>Nanoscale, 2018-06, Vol.10 (24), p.11604-11615</ispartof><rights>Copyright Royal Society of Chemistry 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c351t-63731c30d7438ca429604000e47db8b77bb029010c96846cced5118a2aba6a493</citedby><cites>FETCH-LOGICAL-c351t-63731c30d7438ca429604000e47db8b77bb029010c96846cced5118a2aba6a493</cites><orcidid>0000-0002-0701-7695 ; 0000-0002-3183-0504 ; 0000-0001-9652-5765 ; 0000-0002-5587-953X ; 0000-0003-3223-8024</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29892760$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Frontiñán-Rubio, Javier</creatorcontrib><creatorcontrib>Gómez, M Victoria</creatorcontrib><creatorcontrib>Martín, Cristina</creatorcontrib><creatorcontrib>González-Domínguez, Jose M</creatorcontrib><creatorcontrib>Durán-Prado, Mario</creatorcontrib><creatorcontrib>Vázquez, Ester</creatorcontrib><title>Differential effects of graphene materials on the metabolism and function of human skin cells</title><title>Nanoscale</title><addtitle>Nanoscale</addtitle><description>Graphene-related materials (GRMs) such as graphene oxide (GO) and few-layer graphene (FLG) are used in multiple biomedical applications; however, there is still insufficient information available regarding their interactions with the main biological barriers such as skin. In this study, we explored the effects of GO and FLG on HaCaTs human skin keratinocytes, using NMR-based metabolomics and fluorescence microscopy to evaluate the global impact of each GRM on cell fate and damage. GO and FLG at low concentrations (5 μg mL-1) induced a differential remodeling of the metabolome, preceded by an increase in the level of radical oxygen species (ROS) and free cytosolic Ca2+. These changes are linked to a concentration-dependent increase in cell death by triggering apoptosis and necrosis, the latter being predominant at higher concentrations of the nanostructures. In addition, both compounds reduce the ability of HaCaT cells to heal wounds. Our results demonstrate that the GO and FLG used in this study, which mainly differ in their oxidation state, slightly trigger differential effects on HaCaTs cells, but with evident outcomes at the cellular and molecular levels. Their behavior as pro-apoptotic/necrotic substances and their ability to inhibit cell migration, even at low doses, should be considered in the development of future applications.</description><subject>Apoptosis</subject><subject>Biomedical materials</subject><subject>Calcium ions</subject><subject>Cell adhesion & migration</subject><subject>Cell death</subject><subject>Cell Line</subject><subject>Fluorescence</subject><subject>Graphene</subject><subject>Graphite - pharmacology</subject><subject>Humans</subject><subject>Impact damage</subject><subject>Keratinocytes - drug effects</subject><subject>Low concentrations</subject><subject>Metabolism</subject><subject>Molecular chains</subject><subject>Nanostructures</subject><subject>Necrosis</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Oxidation</subject><subject>Oxides</subject><subject>Reactive Oxygen Species</subject><subject>Skin</subject><subject>Skin - cytology</subject><subject>Skin - drug effects</subject><subject>Valence</subject><issn>2040-3364</issn><issn>2040-3372</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9UMlOwzAQtRCIlsKFD0CWuCEFxnbi5YjCKlUgITiiyHEcmtI4xXYO_D2Glp7mad4yo4fQKYFLAkxdGek8gFTC7KEphRwyxgTd32GeT9BRCEsArhhnh2hClVRUcJii95uuba23LnZ6hW3CJgY8tPjD6_XCOot7Ha1PZNo6HBdpYaOuh1UXeqxdg9vRmdglLpkWY68dDp-dw8auVuEYHbTJaU-2c4be7m5fy4ds_nz_WF7PM8MKEjPOBCOGQSNyJo3OqeLpcwCbi6aWtRB1DVQBAaO4zLkxtikIkZrqWnOdKzZD55vctR--RhtitRxG79LJikIhCsYlg6S62KiMH0Lwtq3Wvuu1_64IVL9NVqV8evlrskzis23kWPe22Un_q2M_xR5trw</recordid><startdate>20180628</startdate><enddate>20180628</enddate><creator>Frontiñán-Rubio, Javier</creator><creator>Gómez, M Victoria</creator><creator>Martín, Cristina</creator><creator>González-Domínguez, Jose M</creator><creator>Durán-Prado, Mario</creator><creator>Vázquez, Ester</creator><general>Royal Society of Chemistry</general><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>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0002-0701-7695</orcidid><orcidid>https://orcid.org/0000-0002-3183-0504</orcidid><orcidid>https://orcid.org/0000-0001-9652-5765</orcidid><orcidid>https://orcid.org/0000-0002-5587-953X</orcidid><orcidid>https://orcid.org/0000-0003-3223-8024</orcidid></search><sort><creationdate>20180628</creationdate><title>Differential effects of graphene materials on the metabolism and function of human skin cells</title><author>Frontiñán-Rubio, Javier ; 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however, there is still insufficient information available regarding their interactions with the main biological barriers such as skin. In this study, we explored the effects of GO and FLG on HaCaTs human skin keratinocytes, using NMR-based metabolomics and fluorescence microscopy to evaluate the global impact of each GRM on cell fate and damage. GO and FLG at low concentrations (5 μg mL-1) induced a differential remodeling of the metabolome, preceded by an increase in the level of radical oxygen species (ROS) and free cytosolic Ca2+. These changes are linked to a concentration-dependent increase in cell death by triggering apoptosis and necrosis, the latter being predominant at higher concentrations of the nanostructures. In addition, both compounds reduce the ability of HaCaT cells to heal wounds. Our results demonstrate that the GO and FLG used in this study, which mainly differ in their oxidation state, slightly trigger differential effects on HaCaTs cells, but with evident outcomes at the cellular and molecular levels. 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subjects | Apoptosis Biomedical materials Calcium ions Cell adhesion & migration Cell death Cell Line Fluorescence Graphene Graphite - pharmacology Humans Impact damage Keratinocytes - drug effects Low concentrations Metabolism Molecular chains Nanostructures Necrosis NMR Nuclear magnetic resonance Oxidation Oxides Reactive Oxygen Species Skin Skin - cytology Skin - drug effects Valence |
title | Differential effects of graphene materials on the metabolism and function of human skin cells |
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