Skip directly to search Skip directly to A to Z list Skip directly to page options Skip directly to site content

NIOSHTIC-2 Publications Search

Search Results

Effects of copper nanoparticle exposure on host defense in a murine pulmonary infection model.

Kim-JS; Adamcakova-Dodd-A; O'Shaughnessy-PT; Grassian-VH; Thorne-PS
Part Fibre Toxicol 2011 Sep; 8:29
BACKGROUND: Human exposure to nanoparticles (NPs) and environmental bacteria can occur simultaneously. NPs induce inflammatory responses and oxidative stress but may also have immune-suppressive effects, impairing macrophage function and altering epithelial barrier functions. The purpose of this study was to assess the potential pulmonary effects of inhalation and instillation exposure to copper (Cu) NPs using a model of lung inflammation and host defense. METHODS: We used Klebsiella pneumoniae (K.p.) in a murine lung infection model to determine if pulmonary bacterial clearance is enhanced or impaired by Cu NP exposure. Two different exposure modes were tested: sub-acute inhalation (4 hr/day, 5 d/week for 2 weeks, 3.5 mg/m(3)) and intratracheal instillation (24 hr post-exposure, 3, 35, and 100 g/mouse). Pulmonary responses were evaluated by lung histopathology plus measurement of differential cell counts, total protein, lactate dehydrogenase (LDH) activity, and inflammatory cytokines in bronchoalveolar lavage (BAL) fluid. RESULTS: Cu NP exposure induced inflammatory responses with increased recruitment of total cells and neutrophils to the lungs as well as increased total protein and LDH activity in BAL fluid. Both inhalation and instillation exposure to Cu NPs significantly decreased the pulmonary clearance of K.p.-exposed mice measured 24 hr after bacterial infection following Cu NP exposure versus sham-exposed mice also challenged with K.p (1.4 10(5) bacteria/mouse). CONCLUSIONS: Cu NP exposure impaired host defense against bacterial lung infections and induced a dose-dependent decrease in bacterial clearance in which even our lowest dose demonstrated significantly lower clearance than observed in sham-exposed mice. Thus, exposure to Cu NPs may increase the risk of pulmonary infection.
Microbiology; Nanotechnology; Particulates; Environmental-hazards; Environmental-contamination; Bacteria; Bacterial-dusts; Bacterial-infections; Oxidation; Oxidative-processes; Cell-function; Cellular-function; Pulmonary-function; Pulmonary-system; Inhalants; Exposure-levels; Exposure-limits; Copper-compounds; Copper-dust; Copper-nickel-zinc-alloys; Lung; Lung-disorders; Lung-function; Lung-tissue; Models; Respiratory-irritants; Respiratory-system-disorders; Respiration; Respirable-dust; Immunology; Drugs; Drug-interaction; Chemical-hypersensitivity; Author Keywords: Copper; nanoparticles; inhalation; instillation; bacterial clearance; murine; pulmonary infection; Klebsiella pneumoniae
Peter S. Thorne, Interdisciplinary Graduate Program in Human Toxicology, University of Iowa, Iowa City, IA 52242
Publication Date
Document Type
Journal Article
Email Address
Funding Type
Fiscal Year
NTIS Accession No.
NTIS Price
Identifying No.
Grant-Number-R01-OH-009448; B01182012
Source Name
Particle and Fibre Toxicology
Performing Organization
University of Iowa