Interactions of nanoparticles with pulmonary structures and cellular responses
Institute of Anatomy, University of Bern, Bern, Switzerland Submitted 23 October 2007 ; accepted in final form 5 February 2008 Combustion-derived and synthetic nano-sized particles (NSP) have gained considerable interest among pulmonary researchers and clinicians for two main reasons. 1 ) Inhalation...
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Veröffentlicht in: | American journal of physiology. Lung cellular and molecular physiology 2008-05, Vol.294 (5), p.L817-L829 |
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container_title | American journal of physiology. Lung cellular and molecular physiology |
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creator | Muhlfeld, Christian Rothen-Rutishauser, Barbara Blank, Fabian Vanhecke, Dimitri Ochs, Matthias Gehr, Peter |
description | Institute of Anatomy, University of Bern, Bern, Switzerland
Submitted 23 October 2007
; accepted in final form 5 February 2008
Combustion-derived and synthetic nano-sized particles (NSP) have gained considerable interest among pulmonary researchers and clinicians for two main reasons. 1 ) Inhalation exposure to combustion-derived NSP was associated with increased pulmonary and cardiovascular morbidity and mortality as suggested by epidemiological studies. Experimental evidence has provided a mechanistic picture of the adverse health effects associated with inhalation of combustion-derived and synthetic NSP. 2 ) The toxicological potential of NSP contrasts with the potential application of synthetic NSP in technological as well as medicinal settings, with the latter including the use of NSP as diagnostics or therapeutics. To shed light on this paradox, this article aims to highlight recent findings about the interaction of inhaled NSP with the structures of the respiratory tract including surfactant, alveolar macrophages, and epithelial cells. Cellular responses to NSP exposure include the generation of reactive oxygen species and the induction of an inflammatory response. Furthermore, this review places special emphasis on methodological differences between experimental studies and the caveats associated with the dose metrics and points out ways to overcome inherent methodological problems.
ultrafine particles; engineered nanoparticles; electron tomography; translocation; oxidative stress
Address for reprint requests and other correspondence: C. Mühlfeld, Institute of Anatomy, Univ. of Bern, Baltzerstrasse 2, CH-3000 Bern 9, Switzerland (e-mail: muehlfeld{at}ana.unibe.ch ) |
doi_str_mv | 10.1152/ajplung.00442.2007 |
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Submitted 23 October 2007
; accepted in final form 5 February 2008
Combustion-derived and synthetic nano-sized particles (NSP) have gained considerable interest among pulmonary researchers and clinicians for two main reasons. 1 ) Inhalation exposure to combustion-derived NSP was associated with increased pulmonary and cardiovascular morbidity and mortality as suggested by epidemiological studies. Experimental evidence has provided a mechanistic picture of the adverse health effects associated with inhalation of combustion-derived and synthetic NSP. 2 ) The toxicological potential of NSP contrasts with the potential application of synthetic NSP in technological as well as medicinal settings, with the latter including the use of NSP as diagnostics or therapeutics. To shed light on this paradox, this article aims to highlight recent findings about the interaction of inhaled NSP with the structures of the respiratory tract including surfactant, alveolar macrophages, and epithelial cells. Cellular responses to NSP exposure include the generation of reactive oxygen species and the induction of an inflammatory response. Furthermore, this review places special emphasis on methodological differences between experimental studies and the caveats associated with the dose metrics and points out ways to overcome inherent methodological problems.
ultrafine particles; engineered nanoparticles; electron tomography; translocation; oxidative stress
Address for reprint requests and other correspondence: C. Mühlfeld, Institute of Anatomy, Univ. of Bern, Baltzerstrasse 2, CH-3000 Bern 9, Switzerland (e-mail: muehlfeld{at}ana.unibe.ch )</description><identifier>ISSN: 1040-0605</identifier><identifier>EISSN: 1522-1504</identifier><identifier>DOI: 10.1152/ajplung.00442.2007</identifier><identifier>PMID: 18263666</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Cells ; Drug Delivery Systems ; Experiments ; Humans ; Inhalation Exposure ; Lungs ; Nanoparticles ; Nanoparticles - adverse effects ; Nanoparticles - therapeutic use ; Oxidation ; Oxidative Stress ; Pulmonary Alveoli - cytology ; Pulmonary Alveoli - metabolism ; Respiratory Mucosa - cytology ; Respiratory Mucosa - metabolism ; Tomography</subject><ispartof>American journal of physiology. Lung cellular and molecular physiology, 2008-05, Vol.294 (5), p.L817-L829</ispartof><rights>Copyright American Physiological Society May 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c485t-306db1777a40eeec069fddfed6b9aa80ca2267234ab838be9be18f69c91ed9853</citedby><cites>FETCH-LOGICAL-c485t-306db1777a40eeec069fddfed6b9aa80ca2267234ab838be9be18f69c91ed9853</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3037,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18263666$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Muhlfeld, Christian</creatorcontrib><creatorcontrib>Rothen-Rutishauser, Barbara</creatorcontrib><creatorcontrib>Blank, Fabian</creatorcontrib><creatorcontrib>Vanhecke, Dimitri</creatorcontrib><creatorcontrib>Ochs, Matthias</creatorcontrib><creatorcontrib>Gehr, Peter</creatorcontrib><title>Interactions of nanoparticles with pulmonary structures and cellular responses</title><title>American journal of physiology. Lung cellular and molecular physiology</title><addtitle>Am J Physiol Lung Cell Mol Physiol</addtitle><description>Institute of Anatomy, University of Bern, Bern, Switzerland
Submitted 23 October 2007
; accepted in final form 5 February 2008
Combustion-derived and synthetic nano-sized particles (NSP) have gained considerable interest among pulmonary researchers and clinicians for two main reasons. 1 ) Inhalation exposure to combustion-derived NSP was associated with increased pulmonary and cardiovascular morbidity and mortality as suggested by epidemiological studies. Experimental evidence has provided a mechanistic picture of the adverse health effects associated with inhalation of combustion-derived and synthetic NSP. 2 ) The toxicological potential of NSP contrasts with the potential application of synthetic NSP in technological as well as medicinal settings, with the latter including the use of NSP as diagnostics or therapeutics. To shed light on this paradox, this article aims to highlight recent findings about the interaction of inhaled NSP with the structures of the respiratory tract including surfactant, alveolar macrophages, and epithelial cells. Cellular responses to NSP exposure include the generation of reactive oxygen species and the induction of an inflammatory response. Furthermore, this review places special emphasis on methodological differences between experimental studies and the caveats associated with the dose metrics and points out ways to overcome inherent methodological problems.
ultrafine particles; engineered nanoparticles; electron tomography; translocation; oxidative stress
Address for reprint requests and other correspondence: C. Mühlfeld, Institute of Anatomy, Univ. of Bern, Baltzerstrasse 2, CH-3000 Bern 9, Switzerland (e-mail: muehlfeld{at}ana.unibe.ch )</description><subject>Animals</subject><subject>Cells</subject><subject>Drug Delivery Systems</subject><subject>Experiments</subject><subject>Humans</subject><subject>Inhalation Exposure</subject><subject>Lungs</subject><subject>Nanoparticles</subject><subject>Nanoparticles - adverse effects</subject><subject>Nanoparticles - therapeutic use</subject><subject>Oxidation</subject><subject>Oxidative Stress</subject><subject>Pulmonary Alveoli - cytology</subject><subject>Pulmonary Alveoli - metabolism</subject><subject>Respiratory Mucosa - cytology</subject><subject>Respiratory Mucosa - metabolism</subject><subject>Tomography</subject><issn>1040-0605</issn><issn>1522-1504</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1u3CAURlHVqEmTvEAXldW9pxeMMSyrqGkjjdJNskYYX894xBiXH6Xz9iGdibLKCsT9zgccQr5QWFHasu9mt7g8b1YAnLMVA-g-kIsyYDVtgX8se-BQg4D2nHyOcQcALYD4RM6pZKIRQlyQ-7s5YTA2TX6OlR-r2cx-MSFN1mGsnqa0rZbs9n424VDFFLJNOZSJmYfKonPZmVCVg6XwGK_I2WhcxOvTekkeb38-3Pyu139-3d38WNeWyzbVDYihp13XGQ6IaEGocRhGHESvjJFgDWOiYw03vWxkj6pHKkehrKI4KNk2l-TbsXcJ_m_GmPTO5zCXKzWjoJiElpcQO4Zs8DEGHPUSpn35h6agXwzqk0H936B-MVigr6fm3O9xeENOykpAHQPbabN9mgLqZXuIk3d-c9C32bkH_Jdem5niutVrSTu9DGNh6_fZ18e8Mc0zVM2VcA</recordid><startdate>20080501</startdate><enddate>20080501</enddate><creator>Muhlfeld, Christian</creator><creator>Rothen-Rutishauser, Barbara</creator><creator>Blank, Fabian</creator><creator>Vanhecke, Dimitri</creator><creator>Ochs, Matthias</creator><creator>Gehr, Peter</creator><general>American Physiological Society</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>7QP</scope><scope>7TS</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20080501</creationdate><title>Interactions of nanoparticles with pulmonary structures and cellular responses</title><author>Muhlfeld, Christian ; Rothen-Rutishauser, Barbara ; Blank, Fabian ; Vanhecke, Dimitri ; Ochs, Matthias ; Gehr, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c485t-306db1777a40eeec069fddfed6b9aa80ca2267234ab838be9be18f69c91ed9853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Cells</topic><topic>Drug Delivery Systems</topic><topic>Experiments</topic><topic>Humans</topic><topic>Inhalation Exposure</topic><topic>Lungs</topic><topic>Nanoparticles</topic><topic>Nanoparticles - adverse effects</topic><topic>Nanoparticles - therapeutic use</topic><topic>Oxidation</topic><topic>Oxidative Stress</topic><topic>Pulmonary Alveoli - cytology</topic><topic>Pulmonary Alveoli - metabolism</topic><topic>Respiratory Mucosa - cytology</topic><topic>Respiratory Mucosa - metabolism</topic><topic>Tomography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Muhlfeld, Christian</creatorcontrib><creatorcontrib>Rothen-Rutishauser, Barbara</creatorcontrib><creatorcontrib>Blank, Fabian</creatorcontrib><creatorcontrib>Vanhecke, Dimitri</creatorcontrib><creatorcontrib>Ochs, Matthias</creatorcontrib><creatorcontrib>Gehr, Peter</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>American journal of physiology. Lung cellular and molecular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Muhlfeld, Christian</au><au>Rothen-Rutishauser, Barbara</au><au>Blank, Fabian</au><au>Vanhecke, Dimitri</au><au>Ochs, Matthias</au><au>Gehr, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interactions of nanoparticles with pulmonary structures and cellular responses</atitle><jtitle>American journal of physiology. Lung cellular and molecular physiology</jtitle><addtitle>Am J Physiol Lung Cell Mol Physiol</addtitle><date>2008-05-01</date><risdate>2008</risdate><volume>294</volume><issue>5</issue><spage>L817</spage><epage>L829</epage><pages>L817-L829</pages><issn>1040-0605</issn><eissn>1522-1504</eissn><abstract>Institute of Anatomy, University of Bern, Bern, Switzerland
Submitted 23 October 2007
; accepted in final form 5 February 2008
Combustion-derived and synthetic nano-sized particles (NSP) have gained considerable interest among pulmonary researchers and clinicians for two main reasons. 1 ) Inhalation exposure to combustion-derived NSP was associated with increased pulmonary and cardiovascular morbidity and mortality as suggested by epidemiological studies. Experimental evidence has provided a mechanistic picture of the adverse health effects associated with inhalation of combustion-derived and synthetic NSP. 2 ) The toxicological potential of NSP contrasts with the potential application of synthetic NSP in technological as well as medicinal settings, with the latter including the use of NSP as diagnostics or therapeutics. To shed light on this paradox, this article aims to highlight recent findings about the interaction of inhaled NSP with the structures of the respiratory tract including surfactant, alveolar macrophages, and epithelial cells. Cellular responses to NSP exposure include the generation of reactive oxygen species and the induction of an inflammatory response. Furthermore, this review places special emphasis on methodological differences between experimental studies and the caveats associated with the dose metrics and points out ways to overcome inherent methodological problems.
ultrafine particles; engineered nanoparticles; electron tomography; translocation; oxidative stress
Address for reprint requests and other correspondence: C. Mühlfeld, Institute of Anatomy, Univ. of Bern, Baltzerstrasse 2, CH-3000 Bern 9, Switzerland (e-mail: muehlfeld{at}ana.unibe.ch )</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>18263666</pmid><doi>10.1152/ajplung.00442.2007</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cells Drug Delivery Systems Experiments Humans Inhalation Exposure Lungs Nanoparticles Nanoparticles - adverse effects Nanoparticles - therapeutic use Oxidation Oxidative Stress Pulmonary Alveoli - cytology Pulmonary Alveoli - metabolism Respiratory Mucosa - cytology Respiratory Mucosa - metabolism Tomography |
title | Interactions of nanoparticles with pulmonary structures and cellular responses |
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