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Pulmonary exposure to single-walled carbon nanotubes does not affect the early immune response against Toxoplasma gondii
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نویسنده
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swedin l. ,arrighi r. ,andersson-willman b. ,murray a. ,chen y. ,karlsson m.c.i. ,georén s.k. ,tkach a.v. ,shvedova a.a. ,fadeel b. ,barragan a. ,scheynius a.
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منبع
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particle and fibre toxicology - 2012 - دوره : 9 - شماره : 0
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چکیده
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Background: single-walled carbon nanotubes (swcnt) trigger pronounced inflammation and fibrosis in the lungs of mice following administration via pharyngeal aspiration or inhalation. human exposure to swcnt in an occupational setting may occur in conjunction with infections and this could yield enhanced or suppressed responses to the offending agent. here,we studied whether the sequential exposure to swcnt via pharyngeal aspiration and infection of mice with the ubiquitous intracellular parasite toxoplasma gondii would impact on the immune response of the host against the parasite.methods: c57bl/6 mice were pre-exposed by pharyngeal administration of swcnt (80 + 80 μg/mouse) for two consecutive days followed by intravenous injection with either 1x103 or 1x104 green fluorescence protein and luciferase-expressing t. gondii tachyzoites. the dissemination of t. gondii was monitored by in vivo bioluminescence imaging in real time for 7 days and by plaque formation. the inflammatory response was analysed in bronchoalveolar lavage (bal) fluid,and by assessment of morphological changes and immune responses in lung and spleen.results: there were no differences in parasite distribution between mice only inoculated with t. gondii or those mice pre-exposed for 2 days to swcnt before parasite inoculum. lung and spleen histology and inflammation markers in bal fluid reflected the effects of swcnt exposure and t. gondii injection,respectively. we also noted that cd11c positive dendritic cells but not f4/80 positive macrophages retained swcnt in the lungs 9 days after pharyngeal aspiration. however,co-localization of t. gondii with cd11c or f4/80 positive cells could not be observed in lungs or spleen. pre-exposure to swcnt did not affect the splenocyte response to t. gondii.conclusions: taken together,our data indicate that pre-exposure to swcnt does not enhance or suppress the early immune response to t. gondii in mice. © 2012 swedin et al.; licensee biomed central ltd.
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کلیدواژه
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Bioluminescence imaging; Carbon nanotubes; Dendritic cells; Inflammation markers; Lung and spleen immunohistology; Macrophages; Toxoplasma gondii
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آدرس
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institute of environmental medicine,division of molecular toxicology,karolinska institutet,stockholm, Sweden, swedish institute for communicable disease control,stockholm,sweden,center for infectious medicine,department of medicine,karolinska institutet,stockholm, Sweden, translational immunology unit,department of medicine solna,karolinska institutet,stockholm, Sweden, pathology and physiology research branch,health effects laboratory division,national institute for occupational safety and health,center for disease control and prevention,morgantown,wv,united states,department physiology and pharmacology,school of medicine,west virginia university,morgantown,wv, United States, translational immunology unit,department of medicine solna,karolinska institutet,stockholm, Sweden, translational immunology unit,department of medicine solna,karolinska institutet,stockholm, Sweden, department of clinical science,intervention and technology,division of entdiseases,karolinska institutet,stockholm, Sweden, pathology and physiology research branch,health effects laboratory division,national institute for occupational safety and health,center for disease control and prevention,morgantown,wv, United States, pathology and physiology research branch,health effects laboratory division,national institute for occupational safety and health,center for disease control and prevention,morgantown,wv,united states,department physiology and pharmacology,school of medicine,west virginia university,morgantown,wv, United States, institute of environmental medicine,division of molecular toxicology,karolinska institutet,stockholm, Sweden, swedish institute for communicable disease control,stockholm,sweden,center for infectious medicine,department of medicine,karolinska institutet,stockholm, Sweden, translational immunology unit,department of medicine solna,karolinska institutet,stockholm, Sweden
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Authors
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