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Suppression of oocyte glycine transporter activity in mouse cumulus–oocyte complexes before resumption of meiosis
by
Baltz, Jay M.
, Tscherner, Allison K.
in
Acid production
/ Acids
/ Animals
/ Arachidonic acid
/ Cell culture
/ Cell size
/ cell volume regulation
/ cumulus
/ Cumulus Cells - drug effects
/ Cumulus Cells - metabolism
/ Cumulus Cells - physiology
/ Cyclin-dependent kinase
/ Embryos
/ Ethylenediaminetetraacetic acid
/ Female
/ Glycine
/ Glycine Plasma Membrane Transport Proteins - genetics
/ Glycine Plasma Membrane Transport Proteins - metabolism
/ Glycine transporter
/ Meiosis
/ Meiosis - drug effects
/ Meiosis - physiology
/ Mice
/ Natriuretic Peptide, C-Type - pharmacology
/ Natriuretic peptides
/ oocyte
/ Oocytes
/ Oocytes - drug effects
/ Oocytes - metabolism
/ Oocytes - physiology
/ Ovulation
/ Penicillin G
/ Phospholipase
/ Phospholipase A
/ RESEARCH ARTICLE
2025
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Suppression of oocyte glycine transporter activity in mouse cumulus–oocyte complexes before resumption of meiosis
by
Baltz, Jay M.
, Tscherner, Allison K.
in
Acid production
/ Acids
/ Animals
/ Arachidonic acid
/ Cell culture
/ Cell size
/ cell volume regulation
/ cumulus
/ Cumulus Cells - drug effects
/ Cumulus Cells - metabolism
/ Cumulus Cells - physiology
/ Cyclin-dependent kinase
/ Embryos
/ Ethylenediaminetetraacetic acid
/ Female
/ Glycine
/ Glycine Plasma Membrane Transport Proteins - genetics
/ Glycine Plasma Membrane Transport Proteins - metabolism
/ Glycine transporter
/ Meiosis
/ Meiosis - drug effects
/ Meiosis - physiology
/ Mice
/ Natriuretic Peptide, C-Type - pharmacology
/ Natriuretic peptides
/ oocyte
/ Oocytes
/ Oocytes - drug effects
/ Oocytes - metabolism
/ Oocytes - physiology
/ Ovulation
/ Penicillin G
/ Phospholipase
/ Phospholipase A
/ RESEARCH ARTICLE
2025
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Suppression of oocyte glycine transporter activity in mouse cumulus–oocyte complexes before resumption of meiosis
by
Baltz, Jay M.
, Tscherner, Allison K.
in
Acid production
/ Acids
/ Animals
/ Arachidonic acid
/ Cell culture
/ Cell size
/ cell volume regulation
/ cumulus
/ Cumulus Cells - drug effects
/ Cumulus Cells - metabolism
/ Cumulus Cells - physiology
/ Cyclin-dependent kinase
/ Embryos
/ Ethylenediaminetetraacetic acid
/ Female
/ Glycine
/ Glycine Plasma Membrane Transport Proteins - genetics
/ Glycine Plasma Membrane Transport Proteins - metabolism
/ Glycine transporter
/ Meiosis
/ Meiosis - drug effects
/ Meiosis - physiology
/ Mice
/ Natriuretic Peptide, C-Type - pharmacology
/ Natriuretic peptides
/ oocyte
/ Oocytes
/ Oocytes - drug effects
/ Oocytes - metabolism
/ Oocytes - physiology
/ Ovulation
/ Penicillin G
/ Phospholipase
/ Phospholipase A
/ RESEARCH ARTICLE
2025
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Suppression of oocyte glycine transporter activity in mouse cumulus–oocyte complexes before resumption of meiosis
Journal Article
Suppression of oocyte glycine transporter activity in mouse cumulus–oocyte complexes before resumption of meiosis
2025
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Overview
Glycine is a key regulator of cell volume in early preimplantation mouse embryos and supports embryo viability. Its accumulation is initiated when the GLYT1 glycine transporter (SLC6A9) is activated in oocytes at about the same time the oocyte is released from meiotic arrest at the germinal vesicle (GV) stage. The mechanism by which GLYT1 is maintained in an inactive state before ovulation is triggered is unknown. Here, we have shown that GLYT1 activity can remain suppressed in isolated cumulus–oocyte complexes (COCs) under defined culture conditions that include keeping COCs physically separated and using the physiological mediator of GV arrest, natriuretic peptide precursor C. When GV arrest is instead maintained in oocytes within COCs by inhibiting phosphodiesterase 3A or cyclin-dependent kinase 1, GLYT1 similarly remains inactive. However, GLYT1 becomes activated in isolated GV oocytes similarly maintained in GV arrest, indicating that cumulus cells are required for suppressing GLYT1 activity. This implies that meiotic arrest is necessary but not sufficient for preventing GLYT1 activation and that an inhibitory factor likely arising from the cumulus is also required. Finally, we have found that pyrrophenone, a selective inhibitor of arachidonic acid production by cytoplasmic phospholipase A alpha, causes GLYT1 to become activated in oocytes within COCs despite maintenance of meiotic arrest of the oocyte. Since arachidonic acid levels decrease in oocytes after release from GV arrest, we propose that arachidonic acid may be a candidate for the inhibitory factor in COCs that regulates GLYT1 activity. Summary Sentence Suppression of activation of the volume-regulatory glycine transporter GLYT1 in mouse oocytes requires meiotic arrest via cGMP and a cumulus-derived signal that may involve cytoplasmic phospholipase A alpha-produced arachidonic acid. Graphical Abstract
Publisher
Society for the Study of Reproduction,Oxford University Press
Subject
/ Acids
/ Animals
/ cumulus
/ Cumulus Cells - drug effects
/ Embryos
/ Ethylenediaminetetraacetic acid
/ Female
/ Glycine
/ Glycine Plasma Membrane Transport Proteins - genetics
/ Glycine Plasma Membrane Transport Proteins - metabolism
/ Meiosis
/ Mice
/ Natriuretic Peptide, C-Type - pharmacology
/ oocyte
/ Oocytes
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