Open AccessConstitutive IP3R1-mediated Ca2+ release reduces Ca2+ store content and stimulates mitochondrial metabolism in mouse GV oocytes
Author(s) -
Toshifumi Wakai,
Rafael A. Fissore
Publication year - 2019
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.225441
Subject(s) - biology , germinal vesicle , endoplasmic reticulum , microbiology and biotechnology , inositol , mitochondrion , oocyte , inositol trisphosphate receptor , downregulation and upregulation , intracellular , serca , receptor , biochemistry , embryo , atpase , gene , enzyme
In mammals, fertilization initiates Ca2+ oscillations in metaphase II oocytes that are required for the activation of embryo development. Germinal vesicle (GV) oocytes also display Ca2+ oscillations, although they unfold spontaneously in the absence of any known agonist(s) and their function remain unclear. We found that the main intracellular store of Ca2+ in GV oocytes, the endoplasmic reticulum ([Ca2+]ER), constitutively “leaks” Ca2+ through the type 1 inositol 1,4,5-trisphosphate receptor. The [Ca2+]ER leak ceases around the resumption of meiosis, the GVBD stage, which coincides with the first noticeable accumulation of Ca2+ in the stores. It also concurs with downregulation of the Ca2+ influx and termination of the oscillations, which seemed underpinned by the inactivation of the putative plasma membrane Ca2+ channels. Lastly, we demonstrate that mitochondria uptake Ca2+ during the Ca2+ oscillations mounting their own oscillations, which stimulate the mitochondrial redox state and increase the ATP levels of GV oocytes. These distinct features of Ca2+ homeostasis in GV oocytes are likely to underpin the acquisition of both maturation and developmental competence as well as fulfill stage-specific cellular functions during oocyte maturation.