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  • Wang, C. (author)

The toxic effects of microcystin-LR on mouse lungs and alveolar type II epithelial cells

  • Article/chapterEnglish2016

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  • Elsevier BV,2016

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  • LIBRIS-ID:oai:gup.ub.gu.se/236990
  • https://gup.ub.gu.se/publication/236990URI
  • https://doi.org/10.1016/j.toxicon.2016.03.007DOI

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  • Language:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

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  • Objectives: Microcystin-leucine arginine (MC-LR) is produced by cyanobacteria and can accumulate in lungs through blood circulation. However, the effect of MC-LR on lung remains unclear. In this study, we investigated the chronic, low-dose effect of MC-LR on mouse lung tissues and the influence of MC-LR on mouse alveolar type II epithelial cells (ATII cells). Methods: MC-LR was orally administered to mice at 0, 1, 10, and 40 mu g/L for 6 consecutive months and mouse lungs were obtained for histopathological and immunoblot analysis. ATII cells were cultured in various concentrations of MC-LR (0, 0.5, 5, 50, 500 nmol/L) for indicated time and the cell viability and proteins change were tested. Results: Our study revealed that the chronic, low-dose MC-LR exposure induced alveolar collapse and lung cell apoptosis as well as the breach of cell junction integrity. Furthermore, following treatment with MC-LR, ATII cells could uptake MC-LR, resulting in apoptosis and disruption of cell junction integrity. Conclusions: These data support the toxic potential of low-dose MC-LR in rendering chronic injury to lung tissues.

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  • Gu, S. (author)
  • Yin, X. Q. (author)
  • Yuan, M. M. (author)
  • Xiang, ZouGothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för mikrobiologi och immunologi,Institute of Biomedicine, Department of Microbiology and Immunology(Swepub:gu)xxiazo (author)
  • Li, Z. T. (author)
  • Cao, H. H. (author)
  • Meng, X. N. (author)
  • Hu, K. B. (author)
  • Han, X. D. (author)
  • Göteborgs universitetInstitutionen för biomedicin, avdelningen för mikrobiologi och immunologi (creator_code:org_t)

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  • In:Toxicon: Elsevier BV115, s. 81-880041-0101

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