RESUMEN
Human exposures to asbestiform elongate mineral particles (EMP) may lead to diffuse fibrosis, lung cancer, malignant mesothelioma and autoimmune diseases. Cleavage fragments (CF) are chemically identical to asbestiform varieties (or habits) of the parent mineral, but no consensus exists on whether to treat them as asbestos from toxicological and regulatory standpoints. Alveolar macrophages (AM) are the first responders to inhaled particulates, participating in clearance and activating other resident and recruited immunocompetent cells, impacting the long-term outcomes. In this study we address how EMP of asbestiform versus non-asbestiform habit affect AM responses. Max Planck Institute (MPI) cells, a non-transformed mouse line that has an AM phenotype and genotype, were treated with mass-, surface area- (s.a.), and particle number- (p.n.) equivalent concentrations of respirable asbestiform and non-asbestiform riebeckite/tremolite EMP for 24 h. Cytotoxicity, cytokines secretion and transcriptional changes were evaluated. At the equal mass, asbestiform EMP were more cytotoxic, however EMP of both habits induced similar LDH leakage and decrease in viability at s.a. and p.n. equivalent doses. DNA damage assessment and cell cycle analysis revealed differences in the modes of cell death between asbestos and respective CF. There was an increase in chemokines, but not pro-inflammatory cytokines after all EMP treatments. Principal component analysis of the cytokine secretion showed close clustering for the s.a. and p.n. equivalent treatments. There were mineral- and habit-specific patterns of gene expression dysregulation at s.a. equivalent doses. Our study reveals the critical nature of EMP morphometric parameters for exposure assessment and dosing approaches used in toxicity studies.
Asunto(s)
Amianto/efectos adversos , Secreciones Corporales/efectos de los fármacos , Citocinas/metabolismo , Macrófagos Alveolares/efectos de los fármacos , Minerales/efectos adversos , Transcripción Genética/efectos de los fármacos , Contaminantes Ocupacionales del Aire/efectos adversos , Animales , Asbestos Anfíboles/efectos adversos , Enfermedades Autoinmunes/inducido químicamente , Enfermedades Autoinmunes/metabolismo , Células Cultivadas , Neoplasias Pulmonares/inducido químicamente , Neoplasias Pulmonares/metabolismo , Macrófagos Alveolares/metabolismo , Mesotelioma Maligno/inducido químicamente , Mesotelioma Maligno/metabolismo , Ratones , Ratones Endogámicos C57BL , Fibras Minerales/efectos adversos , Exposición Profesional/efectos adversos , Tamaño de la Partícula , Material Particulado/efectos adversosRESUMEN
Cellulose nanocrystals (CNC), also known as nanowhiskers, have recently gained much attention due to their biodegradable nature, advantageous chemical and mechanical properties, economic value and renewability thus making them attractive for a wide range of applications. However, before these materials can be considered for potential uses, investigation of their toxicity is prudent. Although CNC exposures are associated with pulmonary inflammation and damage as well as oxidative stress responses and genotoxicity in vivo, studies evaluating cell transformation or tumorigenic potential of CNC's were not previously conducted. In this study, we aimed to assess the neoplastic-like transformation potential of two forms of CNC derived from wood (powder and gel) in human pulmonary epithelial cells (BEAS-2B) in comparison to fibrous tremolite (TF), known to induce lung cancer. Short-term exposure to CNC or TF induced intracellular ROS increase and DNA damage while long-term exposure resulted in neoplastic-like transformation demonstrated by increased cell proliferation, anchorage-independent growth, migration and invasion. The increased proliferative responses were also in-agreement with observed levels of pro-inflammatory cytokines. Based on the hierarchical clustering analysis (HCA) of the inflammatory cytokine responses, CNC powder was segregated from the control and CNC-gel samples. This suggests that CNC may have the ability to influence neoplastic-like transformation events in pulmonary epithelial cells and that such effects are dependent on the type/form of CNC. Further studies focusing on determining and understanding molecular mechanisms underlying potential CNC cell transformation events and their likelihood to induce tumorigenic effects in vivo are highly warranted.
Asunto(s)
Celulosa/toxicidad , Nanopartículas/toxicidad , Celulosa/química , Células Epiteliales/efectos de los fármacos , Humanos , Estudios Longitudinales , Pulmón/efectos de los fármacos , Nanopartículas/química , Estrés Oxidativo/efectos de los fármacos , Pruebas de Toxicidad Crónica , MaderaRESUMEN
This study was carried out in a factory producing multiwalled carbon nanotubes (MWCNTs) by the catalytic chemical vapor deposition method in a pyrolysis reactor. Air samples of the personal breathing areas were collected simultaneously on mixed cellulose ester filters, for analysis by transmission electron microscopy (TEM), and on high-purity quartz filters for thermal-optical analysis of elemental carbon (EC). It is found that the production of MWCNTs is accompanied by the release of the MWCNT structures in the air of different working zones. The concentration of respirable aerosol in the personal breathing areas, averaged over an 8-hour period, ranges from 0.54 to 6.11 µg/m3 based on EC. Airborne MWCNTs were found in the form of agglomerates that range in size from about 1 to 10 µm. These data are consistent with measurements in different plants by two other international groups (from the United States and Sweden) using similar methodology (TEM in combination with EC analysis). In the absence of convincing data on the potential health risks of MWCNTs, and following the principle of reasonable precautions, preventive measures should be taken to minimize exposure to these materials.
RESUMEN
Nanoscale size and fiber like structure of carbon nanotubes (CNTs) may determine high reactivity and penetration, as well as the pathogenicity of asbestos and other mineral fibers. Despite many in vitro and in vivo studies, the absence of full-scale data on CNT effects on human health clearly point out the necessity for epidemiological studies. Currently, several projects are initiated worldwide on studying health risks associated with the inhalation of industrial CNTs, including NIOSH-promoted research (United States), the European CANTES study, and the Russian CNT-ERA project. Studies comprising several successive steps, such as CNT exposure assessment in occupational settings, toxicological evaluation, and epidemiological observations, are critical for determining material safety and use criteria.
RESUMEN
Local inflammatory response in the lungs and fi brogenic potential of multi-walled carbon nanotubes were studied in an acute aspiration experiment in mice. The doses were chosen based on the concentration of nanotubes in the air at a workplace of the company-producer. ELISA, fl ow cytometry, enhanced darkfield microscopy, and histological examination showed that multi-walled carbon nanotubes induced local inflammation, oxidative stress, and connective tissue growth (fibrosis). Serum levels of TGF-ß1 and osteopontin proteins can serve as potential exposure biomarkers.