Cargando…

SGK regulates pH increase and cyclin B–Cdk1 activation to resume meiosis in starfish ovarian oocytes

Tight regulation of intracellular pH (pH(i)) is essential for biological processes. Fully grown oocytes, having a large nucleus called the germinal vesicle, arrest at meiotic prophase I. Upon hormonal stimulus, oocytes resume meiosis to become fertilizable. At this time, the pH(i) increases via Na(+...

Descripción completa

Detalles Bibliográficos
Autores principales: Hosoda, Enako, Hiraoka, Daisaku, Hirohashi, Noritaka, Omi, Saki, Kishimoto, Takeo, Chiba, Kazuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829648/
https://www.ncbi.nlm.nih.gov/pubmed/31537709
http://dx.doi.org/10.1083/jcb.201812133
_version_ 1783465606642663424
author Hosoda, Enako
Hiraoka, Daisaku
Hirohashi, Noritaka
Omi, Saki
Kishimoto, Takeo
Chiba, Kazuyoshi
author_facet Hosoda, Enako
Hiraoka, Daisaku
Hirohashi, Noritaka
Omi, Saki
Kishimoto, Takeo
Chiba, Kazuyoshi
author_sort Hosoda, Enako
collection PubMed
description Tight regulation of intracellular pH (pH(i)) is essential for biological processes. Fully grown oocytes, having a large nucleus called the germinal vesicle, arrest at meiotic prophase I. Upon hormonal stimulus, oocytes resume meiosis to become fertilizable. At this time, the pH(i) increases via Na(+)/H(+) exchanger activity, although the regulation and function of this change remain obscure. Here, we show that in starfish oocytes, serum- and glucocorticoid-regulated kinase (SGK) is activated via PI3K/TORC2/PDK1 signaling after hormonal stimulus and that SGK is required for this pH(i) increase and cyclin B–Cdk1 activation. When we clamped the pH(i) at 6.7, corresponding to the pH(i) of unstimulated ovarian oocytes, hormonal stimulation induced cyclin B–Cdk1 activation; thereafter, oocytes failed in actin-dependent chromosome transport and spindle assembly after germinal vesicle breakdown. Thus, this SGK-dependent pH(i) increase is likely a prerequisite for these events in ovarian oocytes. We propose a model that SGK drives meiotic resumption via concomitant regulation of the pH(i) and cell cycle machinery.
format Online
Article
Text
id pubmed-6829648
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-68296482019-11-06 SGK regulates pH increase and cyclin B–Cdk1 activation to resume meiosis in starfish ovarian oocytes Hosoda, Enako Hiraoka, Daisaku Hirohashi, Noritaka Omi, Saki Kishimoto, Takeo Chiba, Kazuyoshi J Cell Biol Research Articles Tight regulation of intracellular pH (pH(i)) is essential for biological processes. Fully grown oocytes, having a large nucleus called the germinal vesicle, arrest at meiotic prophase I. Upon hormonal stimulus, oocytes resume meiosis to become fertilizable. At this time, the pH(i) increases via Na(+)/H(+) exchanger activity, although the regulation and function of this change remain obscure. Here, we show that in starfish oocytes, serum- and glucocorticoid-regulated kinase (SGK) is activated via PI3K/TORC2/PDK1 signaling after hormonal stimulus and that SGK is required for this pH(i) increase and cyclin B–Cdk1 activation. When we clamped the pH(i) at 6.7, corresponding to the pH(i) of unstimulated ovarian oocytes, hormonal stimulation induced cyclin B–Cdk1 activation; thereafter, oocytes failed in actin-dependent chromosome transport and spindle assembly after germinal vesicle breakdown. Thus, this SGK-dependent pH(i) increase is likely a prerequisite for these events in ovarian oocytes. We propose a model that SGK drives meiotic resumption via concomitant regulation of the pH(i) and cell cycle machinery. Rockefeller University Press 2019-11-04 2019-09-19 /pmc/articles/PMC6829648/ /pubmed/31537709 http://dx.doi.org/10.1083/jcb.201812133 Text en © 2019 Hosoda et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Articles
Hosoda, Enako
Hiraoka, Daisaku
Hirohashi, Noritaka
Omi, Saki
Kishimoto, Takeo
Chiba, Kazuyoshi
SGK regulates pH increase and cyclin B–Cdk1 activation to resume meiosis in starfish ovarian oocytes
title SGK regulates pH increase and cyclin B–Cdk1 activation to resume meiosis in starfish ovarian oocytes
title_full SGK regulates pH increase and cyclin B–Cdk1 activation to resume meiosis in starfish ovarian oocytes
title_fullStr SGK regulates pH increase and cyclin B–Cdk1 activation to resume meiosis in starfish ovarian oocytes
title_full_unstemmed SGK regulates pH increase and cyclin B–Cdk1 activation to resume meiosis in starfish ovarian oocytes
title_short SGK regulates pH increase and cyclin B–Cdk1 activation to resume meiosis in starfish ovarian oocytes
title_sort sgk regulates ph increase and cyclin b–cdk1 activation to resume meiosis in starfish ovarian oocytes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829648/
https://www.ncbi.nlm.nih.gov/pubmed/31537709
http://dx.doi.org/10.1083/jcb.201812133
work_keys_str_mv AT hosodaenako sgkregulatesphincreaseandcyclinbcdk1activationtoresumemeiosisinstarfishovarianoocytes
AT hiraokadaisaku sgkregulatesphincreaseandcyclinbcdk1activationtoresumemeiosisinstarfishovarianoocytes
AT hirohashinoritaka sgkregulatesphincreaseandcyclinbcdk1activationtoresumemeiosisinstarfishovarianoocytes
AT omisaki sgkregulatesphincreaseandcyclinbcdk1activationtoresumemeiosisinstarfishovarianoocytes
AT kishimototakeo sgkregulatesphincreaseandcyclinbcdk1activationtoresumemeiosisinstarfishovarianoocytes
AT chibakazuyoshi sgkregulatesphincreaseandcyclinbcdk1activationtoresumemeiosisinstarfishovarianoocytes