Length-Dependent Retention of Carbon Nanotubes in the Pleural Space of Mice Initiates Sustained Inflammation and Progressive Fibrosis on the Parietal Pleura
The fibrous shape of carbon nanotubes (CNTs) raises concern that they may pose an asbestos-like inhalation hazard, leading to the development of diseases, especially mesothelioma. Direct instillation of long and short CNTs into the pleural cavity, the site of mesothelioma development, produced asbes...
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| Published in: | The American journal of pathology Vol. 178; no. 6; pp. 2587 - 2600 |
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| Main Authors: | , , , , , , , , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
Bethesda, MD
Elsevier Inc
01-06-2011
American Society for Investigative Pathology American Society for Investigative Pathology / Elsevier |
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| Abstract | The fibrous shape of carbon nanotubes (CNTs) raises concern that they may pose an asbestos-like inhalation hazard, leading to the development of diseases, especially mesothelioma. Direct instillation of long and short CNTs into the pleural cavity, the site of mesothelioma development, produced asbestos-like length-dependent responses. The response to long CNTs and long asbestos was characterized by acute inflammation, leading to progressive fibrosis on the parietal pleura, where stomata of strictly defined size limit the egress of long, but not short, fibers. This was confirmed by demonstrating clearance of short, but not long, CNT and nickel nanowires and by visualizing the migration of short CNTs from the pleural space by single-photon emission computed tomographic imaging. Our data confirm the hypothesis that, although a proportion of all deposited particles passes through the pleura, the pathogenicity of long CNTs and other fibers arises as a result of length-dependent retention at the stomata on the parietal pleura. |
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| AbstractList | The fibrous shape of carbon nanotubes (CNTs) raises concern that they may pose an asbestos-like inhalation hazard, leading to the development of diseases, especially mesothelioma. Direct instillation of long and short CNTs into the pleural cavity, the site of mesothelioma development, produced asbestos-like length-dependent responses. The response to long CNTs and long asbestos was characterized by acute inflammation, leading to progressive fibrosis on the parietal pleura, where stomata of strictly defined size limit the egress of long, but not short, fibers. This was confirmed by demonstrating clearance of short, but not long, CNT and nickel nanowires and by visualizing the migration of short CNTs from the pleural space by single-photon emission computed tomographic imaging. Our data confirm the hypothesis that, although a proportion of all deposited particles passes through the pleura, the pathogenicity of long CNTs and other fibers arises as a result of length-dependent retention at the stomata on the parietal pleura. |
| Author | Ali-Boucetta, Hanene Bianco, Alberto Mather, Stephen J Wallace, William A Kostarelos, Kostas Byrne, Fiona Prina-Mello, Adriele Li, Shouping Nunes, Antonio Murphy, Fiona A Prato, Maurizio MacNee, William Poland, Craig A Al-Jamal, Khuloud T Volkov, Yuri Duffin, Rodger Donaldson, Ken |
| AuthorAffiliation | School of Physics, the Centre for Research on Adaptive Nanostructures and Nanodevices, Trinity College, Dublin, Ireland Department of Pathology, Royal Infirmary of Edinburgh, University of Edinburgh, Edinburgh, United Kingdom University of Edinburgh/Medical Research Council, the Centre for Inflammation Research, Queen's Medical Research Institute, Edinburgh, United Kingdom CNRS, Institut de Biologie Moléculaire et Cellulaire, Immunologie et Chimie Thérapeutiques, Strasbourg, France Safenano, Institute of Occupational Medicine, Edinburgh, United Kingdom Division of Pathology, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, United Kingdom Nanomedicine Laboratory, Centre for Drug Delivery Research, the School of Pharmacy, University of London, London, United Kingdom Department of Pharmaceutical Sciences, Center of Excellence for Nanostructured Materials, University of Trieste, Trieste, Italy Department of Nuclear Medicine, St. Bartholomew's Hospital, London, Unite |
| AuthorAffiliation_xml | – name: School of Medicine, Trinity College, Dublin, Ireland – name: Nanomedicine Laboratory, Centre for Drug Delivery Research, the School of Pharmacy, University of London, London, United Kingdom – name: CNRS, Institut de Biologie Moléculaire et Cellulaire, Immunologie et Chimie Thérapeutiques, Strasbourg, France – name: University of Edinburgh/Medical Research Council, the Centre for Inflammation Research, Queen's Medical Research Institute, Edinburgh, United Kingdom – name: Division of Pathology, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, United Kingdom – name: Department of Nuclear Medicine, St. Bartholomew's Hospital, London, United Kingdom – name: School of Physics, the Centre for Research on Adaptive Nanostructures and Nanodevices, Trinity College, Dublin, Ireland – name: Safenano, Institute of Occupational Medicine, Edinburgh, United Kingdom – name: Department of Pharmaceutical Sciences, Center of Excellence for Nanostructured Materials, University of Trieste, Trieste, Italy – name: Department of Pathology, Royal Infirmary of Edinburgh, University of Edinburgh, Edinburgh, United Kingdom – name: Department of Pharmacy, the Institute of Pharmaceutical Science, King's College London, London, United Kingdom |
| Author_xml | – sequence: 1 fullname: Murphy, Fiona A – sequence: 2 fullname: Poland, Craig A – sequence: 3 fullname: Duffin, Rodger – sequence: 4 fullname: Al-Jamal, Khuloud T – sequence: 5 fullname: Ali-Boucetta, Hanene – sequence: 6 fullname: Nunes, Antonio – sequence: 7 fullname: Byrne, Fiona – sequence: 8 fullname: Prina-Mello, Adriele – sequence: 9 fullname: Volkov, Yuri – sequence: 10 fullname: Li, Shouping – sequence: 11 fullname: Mather, Stephen J – sequence: 12 fullname: Bianco, Alberto – sequence: 13 fullname: Prato, Maurizio – sequence: 14 fullname: MacNee, William – sequence: 15 fullname: Wallace, William A – sequence: 16 fullname: Kostarelos, Kostas – sequence: 17 fullname: Donaldson, Ken |
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| Keywords | Rodentia Inflammation Retention Carbon Progressive Vertebrata Anatomic pathology Mammalia Mouse Length Animal Fibrosis Parietal Pleura |
| Language | English |
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| Publisher | Elsevier Inc American Society for Investigative Pathology American Society for Investigative Pathology / Elsevier |
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| SubjectTerms | Animals Biochemistry, Molecular Biology Biological and medical sciences Cell Proliferation Disease Progression Epithelium - pathology Fibrosis Inflammation - complications Inflammation - pathology Investigative techniques, diagnostic techniques (general aspects) Life Sciences Lymph Nodes - pathology Mediastinum - pathology Medical sciences Mice Molecular biology Nanotubes, Carbon - chemistry Nanotubes, Carbon - ultrastructure Nanowires - ultrastructure Particle Size Pathology Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Pleura - pathology Pleura - ultrastructure Pleural Cavity - pathology Pleural Cavity - ultrastructure Regular Time Factors Tomography, Emission-Computed, Single-Photon Tomography, X-Ray Computed Toxicology |
| Title | Length-Dependent Retention of Carbon Nanotubes in the Pleural Space of Mice Initiates Sustained Inflammation and Progressive Fibrosis on the Parietal Pleura |
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