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
Hauptverfasser: Muhlfeld, Christian, Rothen-Rutishauser, Barbara, Blank, Fabian, Vanhecke, Dimitri, Ochs, Matthias, Gehr, Peter
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container_end_page L829
container_issue 5
container_start_page L817
container_title American journal of physiology. Lung cellular and molecular physiology
container_volume 294
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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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. 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source MEDLINE; American Physiological Society Paid; Alma/SFX Local Collection; EZB Electronic Journals Library
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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