Silver nanoparticles and silver ions cause inflammatory response through induction of cell necrosis and the release of mitochondria in vivo and in vitro
Owing to the excellent antibacterial and antiviral activity, silver nanoparticles have a widespread use in the food and pharmaceutical industries. With the increase in the production and use of the related products, the potential hazard of silver nanoparticles has aroused public attention. The main...
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Veröffentlicht in: | Cell biology and toxicology 2021-04, Vol.37 (2), p.177-191 |
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container_title | Cell biology and toxicology |
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creator | Li, Lu Bi, Zhenfei Hu, Yuzhu Sun, Lu Song, Yanlin Chen, Siyuan Mo, Fei Yang, Jingyun Wei, Yuquan Wei, Xiawei |
description | Owing to the excellent antibacterial and antiviral activity, silver nanoparticles have a widespread use in the food and pharmaceutical industries. With the increase in the production and use of the related products, the potential hazard of silver nanoparticles has aroused public attention. The main purpose of this study is to explore the toxicity of silver nanoparticles and induction of lung inflammation in vitro and in vivo. Here, we validated that small amounts of silver ions dissolved from silver nanoparticles caused the depolarization of plasma membrane, resulting in an overload of intracellular sodium and calcium, and eventually led to the cell necrosis. The blockers of calcium or sodium channels inversed the toxicity of silver ions. Then, we instilled silver nanoparticles or silver nitrate (50 μg per mouse) into the lungs of mice, and this induced pulmonary injury and mitochondrial content release, led to the recruitment of neutrophils to the lung tissue via p38 MAPK pathway. Altogether, these data show that released silver ions from nanoparticles induced cell necrosis through Na
+
and Ca
2+
influx and triggered pulmonary inflammation through elevating mitochondrial-related contents released from these necrotic cells. |
doi_str_mv | 10.1007/s10565-020-09526-4 |
format | Article |
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+
and Ca
2+
influx and triggered pulmonary inflammation through elevating mitochondrial-related contents released from these necrotic cells.</description><identifier>ISSN: 0742-2091</identifier><identifier>EISSN: 1573-6822</identifier><identifier>DOI: 10.1007/s10565-020-09526-4</identifier><identifier>PMID: 32367270</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>A549 Cells ; Animals ; Antiviral activity ; Biochemistry ; Biocompatibility ; Biomedical and Life Sciences ; Calcium ; Calcium (intracellular) ; Calcium - metabolism ; Calcium channels ; Calcium influx ; Calcium ions ; Cell Biology ; Depolarization ; DNA, Mitochondrial - metabolism ; Food industry ; Gold ; GTPase-Activating Proteins - metabolism ; Humans ; Inflammation ; Inflammatory response ; Ions ; Leukocytes (neutrophilic) ; Life Sciences ; Lungs ; MAP kinase ; Membrane potential ; Metal Nanoparticles - adverse effects ; Metal Nanoparticles - ultrastructure ; Mice ; Mice, Inbred C57BL ; Mitochondria ; Mitochondria - drug effects ; Mitochondria - metabolism ; N-Formylmethionine Leucyl-Phenylalanine - pharmacology ; Nanoparticles ; Necroptosis - drug effects ; Necrosis ; Neutrophil Infiltration - drug effects ; Original Article ; Pharmaceutical industry ; Pharmacology/Toxicology ; Pneumonia - pathology ; Protein Kinases - metabolism ; Silver ; Silver - adverse effects ; Silver nitrate ; Sodium ; Sodium - metabolism ; Sodium channels ; Toxicity</subject><ispartof>Cell biology and toxicology, 2021-04, Vol.37 (2), p.177-191</ispartof><rights>Springer Nature B.V. 2020</rights><rights>Springer Nature B.V. 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-21064b17a408ecfc6f896a1ecb2de51de2b9fae660f2c2c802ead0467c17da2a3</citedby><cites>FETCH-LOGICAL-c375t-21064b17a408ecfc6f896a1ecb2de51de2b9fae660f2c2c802ead0467c17da2a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10565-020-09526-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10565-020-09526-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32367270$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Lu</creatorcontrib><creatorcontrib>Bi, Zhenfei</creatorcontrib><creatorcontrib>Hu, Yuzhu</creatorcontrib><creatorcontrib>Sun, Lu</creatorcontrib><creatorcontrib>Song, Yanlin</creatorcontrib><creatorcontrib>Chen, Siyuan</creatorcontrib><creatorcontrib>Mo, Fei</creatorcontrib><creatorcontrib>Yang, Jingyun</creatorcontrib><creatorcontrib>Wei, Yuquan</creatorcontrib><creatorcontrib>Wei, Xiawei</creatorcontrib><title>Silver nanoparticles and silver ions cause inflammatory response through induction of cell necrosis and the release of mitochondria in vivo and in vitro</title><title>Cell biology and toxicology</title><addtitle>Cell Biol Toxicol</addtitle><addtitle>Cell Biol Toxicol</addtitle><description>Owing to the excellent antibacterial and antiviral activity, silver nanoparticles have a widespread use in the food and pharmaceutical industries. With the increase in the production and use of the related products, the potential hazard of silver nanoparticles has aroused public attention. The main purpose of this study is to explore the toxicity of silver nanoparticles and induction of lung inflammation in vitro and in vivo. Here, we validated that small amounts of silver ions dissolved from silver nanoparticles caused the depolarization of plasma membrane, resulting in an overload of intracellular sodium and calcium, and eventually led to the cell necrosis. The blockers of calcium or sodium channels inversed the toxicity of silver ions. Then, we instilled silver nanoparticles or silver nitrate (50 μg per mouse) into the lungs of mice, and this induced pulmonary injury and mitochondrial content release, led to the recruitment of neutrophils to the lung tissue via p38 MAPK pathway. Altogether, these data show that released silver ions from nanoparticles induced cell necrosis through Na
+
and Ca
2+
influx and triggered pulmonary inflammation through elevating mitochondrial-related contents released from these necrotic cells.</description><subject>A549 Cells</subject><subject>Animals</subject><subject>Antiviral activity</subject><subject>Biochemistry</subject><subject>Biocompatibility</subject><subject>Biomedical and Life Sciences</subject><subject>Calcium</subject><subject>Calcium (intracellular)</subject><subject>Calcium - metabolism</subject><subject>Calcium channels</subject><subject>Calcium influx</subject><subject>Calcium ions</subject><subject>Cell Biology</subject><subject>Depolarization</subject><subject>DNA, Mitochondrial - metabolism</subject><subject>Food industry</subject><subject>Gold</subject><subject>GTPase-Activating Proteins - metabolism</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Inflammatory response</subject><subject>Ions</subject><subject>Leukocytes (neutrophilic)</subject><subject>Life Sciences</subject><subject>Lungs</subject><subject>MAP kinase</subject><subject>Membrane potential</subject><subject>Metal Nanoparticles - adverse effects</subject><subject>Metal Nanoparticles - ultrastructure</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mitochondria</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - metabolism</subject><subject>N-Formylmethionine Leucyl-Phenylalanine - pharmacology</subject><subject>Nanoparticles</subject><subject>Necroptosis - drug effects</subject><subject>Necrosis</subject><subject>Neutrophil Infiltration - drug effects</subject><subject>Original Article</subject><subject>Pharmaceutical industry</subject><subject>Pharmacology/Toxicology</subject><subject>Pneumonia - pathology</subject><subject>Protein Kinases - metabolism</subject><subject>Silver</subject><subject>Silver - adverse effects</subject><subject>Silver nitrate</subject><subject>Sodium</subject><subject>Sodium - metabolism</subject><subject>Sodium channels</subject><subject>Toxicity</subject><issn>0742-2091</issn><issn>1573-6822</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kUFv1DAQhS1ERZfCH-CALHHhEjqexHZyRFVpkSpxAM6W15l0XSX2Yicr9Z_wc_FuCkgcOI2l9703Yz3G3gj4IAD0ZRYglawAoYJOoqqaZ2wjpK4r1SI-ZxvQDVYInThnL3N-AAAltHzBzmuslUYNG_bzqx8PlHiwIe5tmr0bKXMbep5XwceQubNLJu7DMNppsnNMjzxR3heJ-LxLcbnfFbVf3FxwHgfuaBx5IJdi9mvcvKPiGckWSwEmP0e3i6FP3hYrP_hDPHGn95ziK3Y22DHT66d5wb5_uv52dVvdfbn5fPXxrnK1lnOFAlSzFdo20JIbnBraTllBbos9SdETbrvBklIwoEPXApLtoVHaCd1btPUFe7_m7lP8sVCezeTz8XwbKC7ZYN21CqVWuqDv_kEf4pJCuc6gBF2rugFZKFyp4-dzosHsk59sejQCzLE3s_ZmSm_m1JtpiuntU_Synaj_Y_ldVAHqFchFCveU_u7-T-wvpL-msw</recordid><startdate>20210401</startdate><enddate>20210401</enddate><creator>Li, Lu</creator><creator>Bi, Zhenfei</creator><creator>Hu, Yuzhu</creator><creator>Sun, Lu</creator><creator>Song, Yanlin</creator><creator>Chen, Siyuan</creator><creator>Mo, Fei</creator><creator>Yang, Jingyun</creator><creator>Wei, Yuquan</creator><creator>Wei, Xiawei</creator><general>Springer Netherlands</general><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7TM</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20210401</creationdate><title>Silver nanoparticles and silver ions cause inflammatory response through induction of cell necrosis and the release of mitochondria in vivo and in vitro</title><author>Li, Lu ; Bi, Zhenfei ; Hu, Yuzhu ; Sun, Lu ; Song, Yanlin ; Chen, Siyuan ; Mo, Fei ; Yang, Jingyun ; Wei, Yuquan ; Wei, Xiawei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-21064b17a408ecfc6f896a1ecb2de51de2b9fae660f2c2c802ead0467c17da2a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>A549 Cells</topic><topic>Animals</topic><topic>Antiviral activity</topic><topic>Biochemistry</topic><topic>Biocompatibility</topic><topic>Biomedical and Life Sciences</topic><topic>Calcium</topic><topic>Calcium (intracellular)</topic><topic>Calcium - metabolism</topic><topic>Calcium channels</topic><topic>Calcium influx</topic><topic>Calcium ions</topic><topic>Cell Biology</topic><topic>Depolarization</topic><topic>DNA, Mitochondrial - metabolism</topic><topic>Food industry</topic><topic>Gold</topic><topic>GTPase-Activating Proteins - metabolism</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Inflammatory response</topic><topic>Ions</topic><topic>Leukocytes (neutrophilic)</topic><topic>Life Sciences</topic><topic>Lungs</topic><topic>MAP kinase</topic><topic>Membrane potential</topic><topic>Metal Nanoparticles - adverse effects</topic><topic>Metal Nanoparticles - ultrastructure</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mitochondria</topic><topic>Mitochondria - drug effects</topic><topic>Mitochondria - metabolism</topic><topic>N-Formylmethionine Leucyl-Phenylalanine - pharmacology</topic><topic>Nanoparticles</topic><topic>Necroptosis - drug effects</topic><topic>Necrosis</topic><topic>Neutrophil Infiltration - drug effects</topic><topic>Original Article</topic><topic>Pharmaceutical industry</topic><topic>Pharmacology/Toxicology</topic><topic>Pneumonia - pathology</topic><topic>Protein Kinases - metabolism</topic><topic>Silver</topic><topic>Silver - adverse effects</topic><topic>Silver nitrate</topic><topic>Sodium</topic><topic>Sodium - metabolism</topic><topic>Sodium channels</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Lu</creatorcontrib><creatorcontrib>Bi, Zhenfei</creatorcontrib><creatorcontrib>Hu, Yuzhu</creatorcontrib><creatorcontrib>Sun, Lu</creatorcontrib><creatorcontrib>Song, Yanlin</creatorcontrib><creatorcontrib>Chen, Siyuan</creatorcontrib><creatorcontrib>Mo, Fei</creatorcontrib><creatorcontrib>Yang, Jingyun</creatorcontrib><creatorcontrib>Wei, Yuquan</creatorcontrib><creatorcontrib>Wei, Xiawei</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cell biology and toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Lu</au><au>Bi, Zhenfei</au><au>Hu, Yuzhu</au><au>Sun, Lu</au><au>Song, Yanlin</au><au>Chen, Siyuan</au><au>Mo, Fei</au><au>Yang, Jingyun</au><au>Wei, Yuquan</au><au>Wei, Xiawei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Silver nanoparticles and silver ions cause inflammatory response through induction of cell necrosis and the release of mitochondria in vivo and in vitro</atitle><jtitle>Cell biology and toxicology</jtitle><stitle>Cell Biol Toxicol</stitle><addtitle>Cell Biol Toxicol</addtitle><date>2021-04-01</date><risdate>2021</risdate><volume>37</volume><issue>2</issue><spage>177</spage><epage>191</epage><pages>177-191</pages><issn>0742-2091</issn><eissn>1573-6822</eissn><abstract>Owing to the excellent antibacterial and antiviral activity, silver nanoparticles have a widespread use in the food and pharmaceutical industries. With the increase in the production and use of the related products, the potential hazard of silver nanoparticles has aroused public attention. The main purpose of this study is to explore the toxicity of silver nanoparticles and induction of lung inflammation in vitro and in vivo. Here, we validated that small amounts of silver ions dissolved from silver nanoparticles caused the depolarization of plasma membrane, resulting in an overload of intracellular sodium and calcium, and eventually led to the cell necrosis. The blockers of calcium or sodium channels inversed the toxicity of silver ions. Then, we instilled silver nanoparticles or silver nitrate (50 μg per mouse) into the lungs of mice, and this induced pulmonary injury and mitochondrial content release, led to the recruitment of neutrophils to the lung tissue via p38 MAPK pathway. Altogether, these data show that released silver ions from nanoparticles induced cell necrosis through Na
+
and Ca
2+
influx and triggered pulmonary inflammation through elevating mitochondrial-related contents released from these necrotic cells.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>32367270</pmid><doi>10.1007/s10565-020-09526-4</doi><tpages>15</tpages></addata></record> |
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subjects | A549 Cells Animals Antiviral activity Biochemistry Biocompatibility Biomedical and Life Sciences Calcium Calcium (intracellular) Calcium - metabolism Calcium channels Calcium influx Calcium ions Cell Biology Depolarization DNA, Mitochondrial - metabolism Food industry Gold GTPase-Activating Proteins - metabolism Humans Inflammation Inflammatory response Ions Leukocytes (neutrophilic) Life Sciences Lungs MAP kinase Membrane potential Metal Nanoparticles - adverse effects Metal Nanoparticles - ultrastructure Mice Mice, Inbred C57BL Mitochondria Mitochondria - drug effects Mitochondria - metabolism N-Formylmethionine Leucyl-Phenylalanine - pharmacology Nanoparticles Necroptosis - drug effects Necrosis Neutrophil Infiltration - drug effects Original Article Pharmaceutical industry Pharmacology/Toxicology Pneumonia - pathology Protein Kinases - metabolism Silver Silver - adverse effects Silver nitrate Sodium Sodium - metabolism Sodium channels Toxicity |
title | Silver nanoparticles and silver ions cause inflammatory response through induction of cell necrosis and the release of mitochondria in vivo and in vitro |
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