<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Barosova, Hana</dc:creator>
  <dc:creator>Maione, Anna G.</dc:creator>
  <dc:creator>Septiadi, Dedy</dc:creator>
  <dc:creator>Sharma, Monita</dc:creator>
  <dc:creator>Haeni, Laetitia</dc:creator>
  <dc:creator>Balog, Sandor</dc:creator>
  <dc:creator>O’Connell, Olivia</dc:creator>
  <dc:creator>Jackson, George R.</dc:creator>
  <dc:creator>Brown, David</dc:creator>
  <dc:creator>Clippinger, Amy J.</dc:creator>
  <dc:creator>Hayden, Patrick</dc:creator>
  <dc:creator>Petri-Fink, Alke</dc:creator>
  <dc:creator>Stone, Vicki</dc:creator>
  <dc:creator>Rothen-Rutishauser, Barbara</dc:creator>
  <dc:date>2020-04-28</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Expansion in production and commercial use of nanomaterials increases the  potential human exposure during the lifecycle of these materials (production,  use, and disposal). Inhalation is a primary route of exposure to nanomaterials;  therefore it is critical to assess their potential respiratory hazard. Herein, we  developed a three-dimensional alveolar model (EpiAlveolar) consisting of  human primary alveolar epithelial cells, fibroblasts, and endothelial cells, with or  without macrophages for predicting long-term responses to aerosols. Following  thorough characterization of the model, proinflammatory and profibrotic  responses based on the adverse outcome pathway concept for lung fibrosis  were assessed upon repeated subchronic exposures (up to 21 days) to two  types of multiwalled carbon nanotubes (MWCNTs) and silica quartz particles.  We simulate occupational exposure doses for the MWCNTs (1–30 μg/cm2)  using an air–liquid interface exposure device (VITROCELL Cloud) with repeated  exposures over 3 weeks. Specific key events leading to lung fibrosis, such as  barrier integrity and release of proinflammatory and profibrotic markers, show  the responsiveness of the model. Nanocyl induced, in general, a less  pronounced reaction than Mitsui-7, and the cultures with human monocyte- derived macrophages (MDMs) showed the proinflammatory response at later  time points than those without MDMs. In conclusion, we present a robust  alveolar model to predict inflammatory and fibrotic responses upon exposure to  MWCNTs.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/308634</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308634/files/fin_uel.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308634/files/fin_uel_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/acsnano.9b06860</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>ACS Nano. - 2020, vol. 14, no. 4, p. 3941–3956</dc:source>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Use of EpiAlveolar lung model to predict fibrotic potential of multiwalled carbon nanotubes</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
