Detailed Information on Publication Record
2016
Apocynin and Diphenyleneiodonium Induce Oxidative Stress and Modulate PI3K/Akt and MAPK/Erk Activity in Mouse Embryonic Stem Cells
KUČERA, Jan, Lucia BINÓ, Kateřina ŠTEFKOVÁ, Josef JAROŠ, Ondřej VAŠÍČEK et. al.Basic information
Original name
Apocynin and Diphenyleneiodonium Induce Oxidative Stress and Modulate PI3K/Akt and MAPK/Erk Activity in Mouse Embryonic Stem Cells
Authors
KUČERA, Jan (203 Czech Republic, belonging to the institution), Lucia BINÓ (703 Slovakia, belonging to the institution), Kateřina ŠTEFKOVÁ (203 Czech Republic, belonging to the institution), Josef JAROŠ (203 Czech Republic, belonging to the institution), Ondřej VAŠÍČEK (203 Czech Republic), Josef VEČEŘA (203 Czech Republic, belonging to the institution), Lukáš KUBALA (203 Czech Republic) and Jiří PACHERNÍK (203 Czech Republic, belonging to the institution)
Edition
Oxidative Medicine and Cellular Longevity, Hindawi Publishing Corporation, 2016, 1942-0900
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
Genetics and molecular biology
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 4.593
RIV identification code
RIV/00216224:14310/16:00089209
Organization unit
Faculty of Science
UT WoS
000369250100001
Keywords in English
NADPH OXIDASE INHIBITOR; SMOOTH-MUSCLE-CELLS; WNT-BETA-CATENIN; REACTIVE OXYGEN; SELF-RENEWAL; CARDIOMYOCYTE DIFFERENTIATION; INTRACELLULAR SUPEROXIDE; ENDOTHELIAL-CELLS; REDOX-REGULATION; FREE-RADICALS
Tags
International impact, Reviewed
Změněno: 30/3/2017 10:12, Ing. Andrea Mikešková
Abstract
V originále
Reactive oxygen species (ROS) are important regulators of cellular functions. In embryonic stem cells, ROS are suggested to influence differentiation status. Regulated ROS formation is catalyzed primarily by NADPH-dependent oxidases (NOXs). Apocynin and diphenyleneiodonium are frequently used inhibitors of NOXs; however, both exhibit uncharacterized effects not related to NOXs inhibition. Interestingly, in our model of mouse embryonic stem cells we demonstrate low expression of NOXs. Therefore we aimed to clarify potential side effects of these drugs. Both apocynin and diphenyleneiodonium impaired proliferation of cells. Surprisingly, we observed prooxidant activity of these drugs determined by hydroethidine. Further, we revealed that apocynin inhibits PI3K/Akt pathway with its downstream transcriptional factor Nanog. Opposite to this, apocynin augmented activity of canonical Wnt signaling. On the contrary, diphenyleneiodonium activated both PI3K/Akt and Erk signaling pathways without affecting Wnt. Our data indicates limits and possible unexpected interactions of NOXs inhibitors with intracellular signaling pathways.
Links
ED3.2.00/08.0144, research and development project |
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EE2.3.20.0180, research and development project |
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EE2.3.30.0009, research and development project |
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LM2010005, research and development project |
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MSM0021622430, plan (intention) |
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MUNI/A/1558/2014, interní kód MU |
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