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Microcystin-LR Does Not Alter Cell Survival and Intracellular Signaling in Human Bronchial Epithelial Cells
O. Brózman, B. Kubickova, P. Babica, P. Laboha
Language English Country Switzerland
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
GJ17-25279Y
Grantová Agentura České Republiky - International
722493
EU Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant NaToxAq to B.K. - International
LM2018121
Czech Ministry of Education, Youth and Sports - International
857560 and 02.1.01/0.0/0.0/18_046/0015975
CETOCOEN EXCELLENCE Teaming 2 project supported by Horizon 2020 and the Czech ministry of Education, Youth and Sports - International
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- MeSH
- Bronchi cytology MeSH
- Cell Line MeSH
- Epithelial Cells drug effects metabolism MeSH
- Extracellular Signal-Regulated MAP Kinases metabolism MeSH
- Humans MeSH
- Microcystins toxicity MeSH
- p38 Mitogen-Activated Protein Kinases metabolism MeSH
- Marine Toxins toxicity MeSH
- Organic Anion Transporters genetics MeSH
- Signal Transduction drug effects MeSH
- Cell Survival drug effects MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Changes in ecological and environmental factors lead to an increased occurrence of cyanobacterial water blooms, while secondary metabolites-producing cyanobacteria pose a threat to both environmental and human health. Apart from oral and dermal exposure, humans may be exposed via inhalation and/or swallowing of contaminated water and aerosols. Although many studies deal with liver toxicity, less information about the effects in the respiratory system is available. We investigated the effects of a prevalent cyanotoxin, microcystin-LR (MC-LR), using respiratory system-relevant human bronchial epithelial (HBE) cells. The expression of specific organic-anion-transporting polypeptides was evaluated, and the western blot analysis revealed the formation and accumulation of MC-LR protein adducts in exposed cells. However, MC-LR up to 20 μM neither caused significant cytotoxic effects according to multiple viability endpoints after 48-h exposure, nor reduced impedance (cell layer integrity) over 96 h. Time-dependent increase of putative MC-LR adducts with protein phosphatases was not associated with activation of mitogen-activated protein kinases ERK1/2 and p38 during 48-h exposure in HBE cells. Future studies addressing human health risks associated with inhalation of toxic cyanobacteria and cyanotoxins should focus on complex environmental samples of cyanobacterial blooms and alterations of additional non-cytotoxic endpoints while adopting more advanced in vitro models.
References provided by Crossref.org
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