Identification of systemic markers from a pulmonary carbon nanotube exposure

J Occup Environ Med. 2011 Jun;53(6 Suppl):S80-6. doi: 10.1097/JOM.0b013e31821ad724.

Abstract

Objective: Interest exists for early monitoring of worker exposure to engineered nanomaterials. Here, we highlight quantitative systemic markers of early effects after carbon nanotube (CNT) exposure.

Methods: Mice were exposed by pharyngeal aspiration to 40-μg CNT and harvested 24 hours, 7 days, and 28 days postexposure for measurements of whole blood, lung and extrapulmonary tissue gene expression, blood and bronchoalveolar lavage (BAL) differentials, and serum protein profiling.

Results: Early effects included increased inflammatory blood gene expression and serum cytokines followed by an acute phase response (eg, CRP, SAA-1, SAP). Beyond 24 hours, there was a consistent increase in blood and BAL eosinophils. At 28 day, serum acute phase proteins with immune function including complement C3, apolipoproteins A-I and A-II, and α₂-macroglobulin were increased.

Conclusions: Carbon nanotube exposure resulted in measurable systemic markers but lacked specificity to distinguish from other pulmonary exposures.

MeSH terms

  • Acute-Phase Proteins / metabolism
  • Animals
  • Aorta / metabolism
  • Biomarkers / blood*
  • Blood Cell Count
  • Blood Coagulation Factors / metabolism
  • Bronchoalveolar Lavage Fluid / chemistry
  • Bronchoalveolar Lavage Fluid / cytology
  • Chemokines / blood
  • Cytokines / blood
  • Eosinophils / metabolism
  • Female
  • Gene Expression*
  • Inflammation / blood
  • Liver / metabolism
  • Lung / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Myocardium / metabolism
  • Nanotubes, Carbon / adverse effects*

Substances

  • Acute-Phase Proteins
  • Biomarkers
  • Blood Coagulation Factors
  • Chemokines
  • Cytokines
  • Nanotubes, Carbon