Lung inflammation and genotoxicity following pulmonary exposure to nanoparticles in ApoE-/- mice

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Lung inflammation and genotoxicity following pulmonary exposure to nanoparticles in ApoE-/- mice. / Jacobsen, Nicklas Raun; Møller, Peter; Jensen, Keld Alstrup; Vogel, Ulla; Ladefoged, Ole; Loft, Steffen; Wallin, Erik Håkan Richard.

In: Particle and Fibre Toxicology, Vol. 6, No. 1, 2009, p. 2.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jacobsen, NR, Møller, P, Jensen, KA, Vogel, U, Ladefoged, O, Loft, S & Wallin, EHR 2009, 'Lung inflammation and genotoxicity following pulmonary exposure to nanoparticles in ApoE-/- mice', Particle and Fibre Toxicology, vol. 6, no. 1, pp. 2. https://doi.org/10.1186/1743-8977-6-2

APA

Jacobsen, N. R., Møller, P., Jensen, K. A., Vogel, U., Ladefoged, O., Loft, S., & Wallin, E. H. R. (2009). Lung inflammation and genotoxicity following pulmonary exposure to nanoparticles in ApoE-/- mice. Particle and Fibre Toxicology, 6(1), 2. https://doi.org/10.1186/1743-8977-6-2

Vancouver

Jacobsen NR, Møller P, Jensen KA, Vogel U, Ladefoged O, Loft S et al. Lung inflammation and genotoxicity following pulmonary exposure to nanoparticles in ApoE-/- mice. Particle and Fibre Toxicology. 2009;6(1):2. https://doi.org/10.1186/1743-8977-6-2

Author

Jacobsen, Nicklas Raun ; Møller, Peter ; Jensen, Keld Alstrup ; Vogel, Ulla ; Ladefoged, Ole ; Loft, Steffen ; Wallin, Erik Håkan Richard. / Lung inflammation and genotoxicity following pulmonary exposure to nanoparticles in ApoE-/- mice. In: Particle and Fibre Toxicology. 2009 ; Vol. 6, No. 1. pp. 2.

Bibtex

@article{1c7392d0f42011ddbf70000ea68e967b,
title = "Lung inflammation and genotoxicity following pulmonary exposure to nanoparticles in ApoE-/- mice",
abstract = "ABSTRACT: BACKGROUND: The toxic and inflammatory potential of 5 different types of nanoparticles were studied in a sensitive model for pulmonary effects in apolipoprotein E knockout mice (ApoE-/-). We studied the effects instillation or inhalation Printex 90 of carbon black (CB) and compared CB instillation in ApoE-/- and C57 mice. Three and 24 h after pulmonary exposure, inflammation was assessed by mRNA levels of cytokines in lung tissue, cell composition, genotoxicity, protein and lactate dehydrogenase activity in broncho-alveolar lavage (BAL) fluid. RESULTS: Firstly, we found that intratracheal instillation of CB caused far more pulmonary toxicity in ApoE-/- mice than in C57 mice. Secondly, we showed that instillation of CB was more toxic than inhalation of a presumed similar dose with respect to inflammation in the lungs of ApoE-/- mice. Thirdly, we compared effects of instillation in ApoE-/- mice of three carbonaceous particles; CB, fullerenes C60 (C60) and single walled carbon nanotubes (SWCNT) as well as gold particles and quantum dots (QDs). Characterization of the instillation media revealed that all particles were delivered as agglomerates and aggregates. Significant increases in Il-6, Mip-2 and Mcp-1 mRNA were detected in lung tissue, 3 h and 24 h following instillation of SWCNT, CB and QDs. DNA damage in BAL cells, the fraction of neutrophils in BAL cells and protein in BAL fluid increased statistically significantly. Gold and C60 particles caused much weaker inflammatory responses. CONCLUSIONS: Our data suggest that ApoE-/- model is sensitive for evaluating particle induced inflammation. Overall QDs had greatest effects followed by CB and SWCNT with C60 and gold being least inflammatory and DNA-damaging. However the gold was used at a much lower mass dose than the other particles. The strong effects of QDs were likely due to Cd release. The surface area of the instilled dose correlated well the inflammatory response for low toxicity particles.",
author = "Jacobsen, {Nicklas Raun} and Peter M{\o}ller and Jensen, {Keld Alstrup} and Ulla Vogel and Ole Ladefoged and Steffen Loft and Wallin, {Erik H{\aa}kan Richard}",
year = "2009",
doi = "10.1186/1743-8977-6-2",
language = "English",
volume = "6",
pages = "2",
journal = "Particle and Fibre Toxicology",
issn = "1743-8977",
publisher = "BioMed Central",
number = "1",

}

RIS

TY - JOUR

T1 - Lung inflammation and genotoxicity following pulmonary exposure to nanoparticles in ApoE-/- mice

AU - Jacobsen, Nicklas Raun

AU - Møller, Peter

AU - Jensen, Keld Alstrup

AU - Vogel, Ulla

AU - Ladefoged, Ole

AU - Loft, Steffen

AU - Wallin, Erik Håkan Richard

PY - 2009

Y1 - 2009

N2 - ABSTRACT: BACKGROUND: The toxic and inflammatory potential of 5 different types of nanoparticles were studied in a sensitive model for pulmonary effects in apolipoprotein E knockout mice (ApoE-/-). We studied the effects instillation or inhalation Printex 90 of carbon black (CB) and compared CB instillation in ApoE-/- and C57 mice. Three and 24 h after pulmonary exposure, inflammation was assessed by mRNA levels of cytokines in lung tissue, cell composition, genotoxicity, protein and lactate dehydrogenase activity in broncho-alveolar lavage (BAL) fluid. RESULTS: Firstly, we found that intratracheal instillation of CB caused far more pulmonary toxicity in ApoE-/- mice than in C57 mice. Secondly, we showed that instillation of CB was more toxic than inhalation of a presumed similar dose with respect to inflammation in the lungs of ApoE-/- mice. Thirdly, we compared effects of instillation in ApoE-/- mice of three carbonaceous particles; CB, fullerenes C60 (C60) and single walled carbon nanotubes (SWCNT) as well as gold particles and quantum dots (QDs). Characterization of the instillation media revealed that all particles were delivered as agglomerates and aggregates. Significant increases in Il-6, Mip-2 and Mcp-1 mRNA were detected in lung tissue, 3 h and 24 h following instillation of SWCNT, CB and QDs. DNA damage in BAL cells, the fraction of neutrophils in BAL cells and protein in BAL fluid increased statistically significantly. Gold and C60 particles caused much weaker inflammatory responses. CONCLUSIONS: Our data suggest that ApoE-/- model is sensitive for evaluating particle induced inflammation. Overall QDs had greatest effects followed by CB and SWCNT with C60 and gold being least inflammatory and DNA-damaging. However the gold was used at a much lower mass dose than the other particles. The strong effects of QDs were likely due to Cd release. The surface area of the instilled dose correlated well the inflammatory response for low toxicity particles.

AB - ABSTRACT: BACKGROUND: The toxic and inflammatory potential of 5 different types of nanoparticles were studied in a sensitive model for pulmonary effects in apolipoprotein E knockout mice (ApoE-/-). We studied the effects instillation or inhalation Printex 90 of carbon black (CB) and compared CB instillation in ApoE-/- and C57 mice. Three and 24 h after pulmonary exposure, inflammation was assessed by mRNA levels of cytokines in lung tissue, cell composition, genotoxicity, protein and lactate dehydrogenase activity in broncho-alveolar lavage (BAL) fluid. RESULTS: Firstly, we found that intratracheal instillation of CB caused far more pulmonary toxicity in ApoE-/- mice than in C57 mice. Secondly, we showed that instillation of CB was more toxic than inhalation of a presumed similar dose with respect to inflammation in the lungs of ApoE-/- mice. Thirdly, we compared effects of instillation in ApoE-/- mice of three carbonaceous particles; CB, fullerenes C60 (C60) and single walled carbon nanotubes (SWCNT) as well as gold particles and quantum dots (QDs). Characterization of the instillation media revealed that all particles were delivered as agglomerates and aggregates. Significant increases in Il-6, Mip-2 and Mcp-1 mRNA were detected in lung tissue, 3 h and 24 h following instillation of SWCNT, CB and QDs. DNA damage in BAL cells, the fraction of neutrophils in BAL cells and protein in BAL fluid increased statistically significantly. Gold and C60 particles caused much weaker inflammatory responses. CONCLUSIONS: Our data suggest that ApoE-/- model is sensitive for evaluating particle induced inflammation. Overall QDs had greatest effects followed by CB and SWCNT with C60 and gold being least inflammatory and DNA-damaging. However the gold was used at a much lower mass dose than the other particles. The strong effects of QDs were likely due to Cd release. The surface area of the instilled dose correlated well the inflammatory response for low toxicity particles.

U2 - 10.1186/1743-8977-6-2

DO - 10.1186/1743-8977-6-2

M3 - Journal article

C2 - 19138394

VL - 6

SP - 2

JO - Particle and Fibre Toxicology

JF - Particle and Fibre Toxicology

SN - 1743-8977

IS - 1

ER -

ID: 10157706