Please use this identifier to cite or link to this item: https://doi.org/10.1186/1465-9921-11-52
Title: Effects of Perfluorocarbons on surfactant exocytosis and membrane properties in isolated alveolar type II cells
Authors: Wemhöner, A
Hackspiel, I
Hobi, N
Ravasio, A 
Haller, T
Rüdiger, M
Keywords: adenosine triphosphate
cell marker
fluorocarbon
flutec
ionomycin
perfluorodecalin
perfluoromethylcyclohexan
phorbol 13 acetate 12 myristate
surfactant
unclassified drug
ionomycin
perfluorodecalin
perfluoromethylcyclohexane
phorbol 13 acetate 12 myristate
surfactant associated protein
animal cell
article
cell isolation
cell membrane fluidity
cell membrane permeability
cell structure
cell viability
controlled study
endocytosis
exocytosis
lung alveolus cell type 2
male
nonhuman
rat
vapor pressure
animal
cell membrane
cell shape
cell survival
drug effect
human
lung alveolus cell
membrane fluidity
metabolism
Sprague Dawley rat
time
tumor cell line
Adenosine Triphosphate
Animals
Cell Line, Tumor
Cell Membrane
Cell Membrane Permeability
Cell Shape
Cell Survival
Exocytosis
Fluorocarbons
Humans
Ionomycin
Male
Membrane Fluidity
Pneumocytes
Pulmonary Surfactant-Associated Proteins
Rats
Rats, Sprague-Dawley
Tetradecanoylphorbol Acetate
Time Factors
Vapor Pressure
Issue Date: 2010
Citation: Wemhöner, A, Hackspiel, I, Hobi, N, Ravasio, A, Haller, T, Rüdiger, M (2010). Effects of Perfluorocarbons on surfactant exocytosis and membrane properties in isolated alveolar type II cells. Respiratory Research 11 : 52. ScholarBank@NUS Repository. https://doi.org/10.1186/1465-9921-11-52
Rights: Attribution 4.0 International
Abstract: 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. © 2010 Wemhöner et al; licensee BioMed Central Ltd.
Source Title: Respiratory Research
URI: https://scholarbank.nus.edu.sg/handle/10635/183266
ISSN: 14659921
DOI: 10.1186/1465-9921-11-52
Rights: Attribution 4.0 International
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