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Expression of the melatonergic system during meiotic maturation of cynomolgus monkey cumulus-oocyte complexesopen access

Authors
Lee, SanghoonKang, Hyo-GuJeong, Pil-SooSong, Bong-SeokChoi, Won SeokJin, Yeung BaeHuh, Jae-WonKim, Sun-UkSim, Bo-Woong
Issue Date
Jun-2023
Publisher
Blackwell Publishing Inc.
Keywords
cumulus-oocyte complex; cynomolgus monkey; melatonin binding site; melatonin membrane receptor; melatonin synthesis enzyme
Citation
Journal of Medical Primatology, v.52, no.3, pp 163 - 169
Pages
7
Indexed
SCIE
SCOPUS
Journal Title
Journal of Medical Primatology
Volume
52
Number
3
Start Page
163
End Page
169
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/30838
DOI
10.1111/jmp.12641
ISSN
0047-2565
1600-0684
Abstract
BackgroundMelatonin is a multifunctional hormone synthesized in the pineal gland and peripheral reproductive tissues that regulates many biological processes. There is increasing evidence for a role of melatonin in oocyte maturation and embryonic development in various mammals. However, no study has reported evidence for the existence of melatonergic system, such as melatonin synthesis enzymes, melatonin membrane receptors, or melatonin binding sites in non-human primate cumulus-oocyte complexes (COCs). MethodsReverse transcription polymerase chain reaction (RT-PCR) and immunocytochemistry were performed to detect transcripts and proteins of the rate-limiting enzyme in melatonin synthesis (arylalkylamine N-acetyltransferase, AANAT), melatonin membrane receptors (MT1 and MT2), and a melatonin binding site (NRH: quinone oxidoreductase 2, NQO2) in cynomolgus monkey COCs. ResultsRT-PCR analyses revealed the presence of AANAT, MT1, MT2, and NQO2 transcripts in granulosa cells, germinal vesicle (GV)- and metaphase II (MII)-stage cumulus cells, and oocytes. Immunocytochemistry revealed the presence of AANAT, MT1, MT2, and NQO2 proteins in GV- and MII-stage COCs. ConclusionsOur results provide the first evidence for the existence of the rate-limiting enzyme required for melatonin synthesis, melatonin membrane receptors, and a melatonin binding site in non-human primate COCs.
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