4.8 Article

Carbon nanotubes degraded by neutrophil myeloperoxidase induce less pulmonary inflammation

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NATURE NANOTECHNOLOGY
卷 5, 期 5, 页码 354-359

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NATURE PORTFOLIO
DOI: 10.1038/NNANO.2010.44

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资金

  1. National Institute for Occupational Safety and Health (NIOSH) [011008282]
  2. National Institutes of Health [HL70755, HL094488, U19AI068021]
  3. National Library of Medicine [LM007994-05]
  4. National Occupational Research Agenda (NORA) [927000Y, 927Z1LU]
  5. Nanotechnology Research Center (NTRC) [927ZJHF]
  6. National Science Foundation (NSF) [0449117]
  7. Air Force Office of Scientific Research (AFOSR) [FA9550-09-1-0478]
  8. European Commission [EC-FP7-NANOMMUNE-214281]
  9. Science Foundation of Ireland
  10. Strategic Research Cluster (SRC) BioNanointeract and Centre for Research on Adaptive Nanostructures and Nanodevices (CRANN)
  11. Higher Education Authority (HEA)
  12. Programme for Research in Third-Level Institutions (PRTLI)
  13. Direct For Computer & Info Scie & Enginr
  14. Division of Computing and Communication Foundations [0449117] Funding Source: National Science Foundation

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We have shown previously that single-walled carbon nanotubes can be catalytically biodegraded over several weeks by the plant-derived enzyme, horseradish peroxidase(1). However, whether peroxidase intermediates generated inside human cells or biofluids are involved in the biodegradation of carbon nanotubes has not been explored. Here, we show that hypochlorite and reactive radical intermediates of the human neutrophil enzyme myeloperoxidase catalyse the biodegradation of single-walled carbon nanotubes in vitro, in neutrophils and to a lesser degree in macrophages. Molecular modelling suggests that interactions of basic amino acids of the enzyme with the carboxyls on the carbon nanotubes position the nanotubes near the catalytic site. Importantly, the biodegraded nanotubes do not generate an inflammatory response when aspirated into the lungs of mice. Our findings suggest that the extent to which carbon nanotubes are biodegraded may be a major determinant of the scale and severity of the associated inflammatory responses in exposed individuals.

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