Melatonin promotes cardiomyogenesis of embryonic stem cells via inhibition of HIF-1α stabilization
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F16%3A00066010" target="_blank" >RIV/00159816:_____/16:00066010 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1111/jpi.12366" target="_blank" >http://dx.doi.org/10.1111/jpi.12366</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1111/jpi.12366" target="_blank" >10.1111/jpi.12366</a>
Alternative languages
Result language
angličtina
Original language name
Melatonin promotes cardiomyogenesis of embryonic stem cells via inhibition of HIF-1α stabilization
Original language description
Melatonin, a molecule involved in the regulation of circadian rhythms, has protective effects against myocardial injuries. However, its capability to regulate the maturation of cardiac progenitor cells is unclear. Recently, several studies have shown that me- latonin inhibits the stabilization of hypoxia- inducible factors (HIFs), important sign- aling molecules with cardioprotective effects. In this study, by employing differentiating mouse embryonic stem cells, we report that melatonin significantly upregulated the expression of cardiac cell- specific markers (myosin heavy chains six and seven) as well as the percentage of myosin heavy chain- positive cells. Importantly, melatonin decreased HIF- 1α stabilization and transcriptional activity and, in con- trast, induced HIF- 2α stabilization. Interestingly, the deletion of HIF- 1α completely inhibited the pro- cardiomyogenic effect of melatonin as well as the melatonin- mediated HIF- 2α stabilization. Moreover, melatonin increased Sirt- 1 levels in a HIF- 1α- dependent manner. Taken together, we provide new evidence of a time- specific inhibition of HIF- 1α stabilization as an essential feature of melatonin- induced car- diomyogenesis and unexpected different roles of HIF- 1α stabilization during various stages of cardiac development. These results uncover new mechanisms underlying the maturation of cardiac progenitor cells and can help in the development of novel strategies for using melatonin in cardiac regeneration therapy.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FH - Neurology, neuro-surgery, nuero-sciences
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2016
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Pineal Research
ISSN
0742-3098
e-ISSN
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Volume of the periodical
61
Issue of the periodical within the volume
4
Country of publishing house
US - UNITED STATES
Number of pages
11
Pages from-to
493-503
UT code for WoS article
000386357100007
EID of the result in the Scopus database
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