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Effects of Perfluorocarbons on surfactant exocytosis and membrane properties in isolated alveolar type II cells
BACKGROUND: Perfluorocarbons (PFC) are used to improve gas exchange in diseased lungs. PFC have been shown to affect various cell types. Thus, effects on alveolar type II (ATII) cells and surfactant metabolism can be expected, data, however, are controversial. OBJECTIVE: The study was performed to t...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2876085/ https://www.ncbi.nlm.nih.gov/pubmed/20459693 http://dx.doi.org/10.1186/1465-9921-11-52 |
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author | Wemhöner, Andreas Hackspiel, Irmgard Hobi, Nina Ravasio, Andrea Haller, Thomas Rüdiger, Mario |
author_facet | Wemhöner, Andreas Hackspiel, Irmgard Hobi, Nina Ravasio, Andrea Haller, Thomas Rüdiger, Mario |
author_sort | Wemhöner, Andreas |
collection | PubMed |
description | BACKGROUND: Perfluorocarbons (PFC) are used to improve gas exchange in diseased lungs. PFC have been shown to affect various cell types. Thus, effects on alveolar type II (ATII) cells and surfactant metabolism can be expected, data, however, are controversial. OBJECTIVE: The study was performed to test two hypotheses: (I) the effects of PFC on surfactant exocytosis depend on their respective vapor pressures; (II) different pathways of surfactant exocytosis are affected differently by PFC. METHODS: Isolated ATII cells were exposed to two PFC with different vapor pressures and spontaneous surfactant exocytosis was measured. Furthermore, surfactant exocytosis was stimulated by either ATP, PMA or Ionomycin. The effects of PFC on cell morphology, cellular viability, endocytosis, membrane permeability and fluidity were determined. RESULTS: The spontaneous exocytosis was reduced by PFC, however, the ATP and PMA stimulated exocytosis was slightly increased by PFC with high vapor pressure. In contrast, Ionomycin-induced exocytosis was decreased by PFC with low vapor pressure. Cellular uptake of FM 1-43 - a marker of membrane integrity - was increased. However, membrane fluidity, endocytosis and viability were not affected by PFC incubation. CONCLUSIONS: We conclude that PFC effects can be explained by modest, unspecific interactions with the plasma membrane rather than by specific interactions with intracellular targets. |
format | Text |
id | pubmed-2876085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28760852010-05-26 Effects of Perfluorocarbons on surfactant exocytosis and membrane properties in isolated alveolar type II cells Wemhöner, Andreas Hackspiel, Irmgard Hobi, Nina Ravasio, Andrea Haller, Thomas Rüdiger, Mario Respir Res Research BACKGROUND: Perfluorocarbons (PFC) are used to improve gas exchange in diseased lungs. PFC have been shown to affect various cell types. Thus, effects on alveolar type II (ATII) cells and surfactant metabolism can be expected, data, however, are controversial. OBJECTIVE: The study was performed to test two hypotheses: (I) the effects of PFC on surfactant exocytosis depend on their respective vapor pressures; (II) different pathways of surfactant exocytosis are affected differently by PFC. METHODS: Isolated ATII cells were exposed to two PFC with different vapor pressures and spontaneous surfactant exocytosis was measured. Furthermore, surfactant exocytosis was stimulated by either ATP, PMA or Ionomycin. The effects of PFC on cell morphology, cellular viability, endocytosis, membrane permeability and fluidity were determined. RESULTS: The spontaneous exocytosis was reduced by PFC, however, the ATP and PMA stimulated exocytosis was slightly increased by PFC with high vapor pressure. In contrast, Ionomycin-induced exocytosis was decreased by PFC with low vapor pressure. Cellular uptake of FM 1-43 - a marker of membrane integrity - was increased. However, membrane fluidity, endocytosis and viability were not affected by PFC incubation. CONCLUSIONS: We conclude that PFC effects can be explained by modest, unspecific interactions with the plasma membrane rather than by specific interactions with intracellular targets. BioMed Central 2010 2010-05-09 /pmc/articles/PMC2876085/ /pubmed/20459693 http://dx.doi.org/10.1186/1465-9921-11-52 Text en Copyright ©2010 Wemhöner et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Wemhöner, Andreas Hackspiel, Irmgard Hobi, Nina Ravasio, Andrea Haller, Thomas Rüdiger, Mario Effects of Perfluorocarbons on surfactant exocytosis and membrane properties in isolated alveolar type II cells |
title | Effects of Perfluorocarbons on surfactant exocytosis and membrane properties in isolated alveolar type II cells |
title_full | Effects of Perfluorocarbons on surfactant exocytosis and membrane properties in isolated alveolar type II cells |
title_fullStr | Effects of Perfluorocarbons on surfactant exocytosis and membrane properties in isolated alveolar type II cells |
title_full_unstemmed | Effects of Perfluorocarbons on surfactant exocytosis and membrane properties in isolated alveolar type II cells |
title_short | Effects of Perfluorocarbons on surfactant exocytosis and membrane properties in isolated alveolar type II cells |
title_sort | effects of perfluorocarbons on surfactant exocytosis and membrane properties in isolated alveolar type ii cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2876085/ https://www.ncbi.nlm.nih.gov/pubmed/20459693 http://dx.doi.org/10.1186/1465-9921-11-52 |
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