J 2020

Microcystin-LR Does Not Alter Cell Survival and Intracellular Signaling in Human Bronchial Epithelial Cells

BRÓZMAN, Ondřej; Barbara KUBÍČKOVÁ; Pavel BABICA a Petra LABOHÁ

Základní údaje

Originální název

Microcystin-LR Does Not Alter Cell Survival and Intracellular Signaling in Human Bronchial Epithelial Cells

Autoři

BRÓZMAN, Ondřej (203 Česká republika, domácí); Barbara KUBÍČKOVÁ (276 Německo, domácí); Pavel BABICA (203 Česká republika, garant, domácí) a Petra LABOHÁ (203 Česká republika, domácí)

Vydání

Toxins, Basel, MDPI, 2020, 2072-6651

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Stát vydavatele

Švýcarsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Kód RIV

RIV/00216224:14310/20:00114249

Organizace

Přírodovědecká fakulta – Masarykova univerzita – Repozitář

UT WoS

000525009500012

EID Scopus

2-s2.0-85081669211

Klíčová slova anglicky

microcystin-LR; human bronchial epithelial cells; in vitro; HBE1; 16HBE14o-; mitogen-activated protein kinase; cytotoxicity; OATP

Návaznosti

EF17_043/0009632, projekt VaV. GJ17-25279Y, projekt VaV. 722493, interní kód Repo. 857560, interní kód Repo. RECETOX RI, velká výzkumná infrastruktura.
Změněno: 4. 6. 2025 00:50, RNDr. Daniel Jakubík

Anotace

V originále

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 mu M 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.

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