<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>Chortarea, Savvina</dc:creator>
  <dc:creator>Barosova, Hana</dc:creator>
  <dc:creator>Clift, Martin J. D.</dc:creator>
  <dc:creator>Wick, Peter</dc:creator>
  <dc:creator>Petri-Fink, Alke</dc:creator>
  <dc:creator>Rothen-Rutishauser, Barbara</dc:creator>
  <dc:date>2017-05-15</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Although acute pulmonary toxicity of carbon nanotubes (CNTs) has been extensively  investigated, the knowledge of potential health effects following chronic occupational  exposure is currently limited and based only upon in vivo approaches. Our aim was to  realistically mimic subchronic inhalation of multiwalled CNTs (MWCNTs) in vitro, using  the air–liquid interface cell exposure (ALICE) system for aerosol exposures on  reconstituted human bronchial tissue from healthy and asthmatic donors. The reliability  and sensitivity of the system were validated using crystalline quartz (DQ12), which  elicited an increased (pro-)inflammatory response, as reported in vivo. At the  administrated MWCNT doses relevant to human occupational lifetime exposure (10  μg/cm2 for 5 weeks of repeated exposures/5 days per week) elevated cilia beating  frequency (in both epithelial cultures), and mucociliary clearance (in asthmatic cells  only) occurred, whereas no cytotoxic reactions or morphological changes were  observed. However, chronic MWCNT exposure did induce an evident  (pro-)inflammatory and oxidative stress response in both healthy and asthmatic cells.  The latter revealed stronger and more durable long-term effects compared to healthy  cells, indicating that individuals with asthma may be more susceptible to adverse  effects from chronic MWCNT exposure. Our results highlight the power of  occupationally relevant subchronic exposures on human in vitro models in nanosafety  hazard assessment.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/305457</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305457/files/fin_hab.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305457/files/fin_hab_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/acsnano.7b01992</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>ACS Nano. - 2017, vol. 11, no. 8, p. 7615-7625</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">air−liquid interface</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">hazard assessment</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">in vitro primary lung system</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">multiwalled carbon nanotubes</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">occupational doses</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">reconstituted healthy and asthma tissue</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">subchronic repeated exposure</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns8="xml" ns8:lang="en">Human asthmatic bronchial cells are more susceptible to subchronic repeated exposures of aerosolized carbon nanotubes at occupationally relevant doses than healthy cells</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
