TY - JOUR
T1 - Ca2+ signaling and homeostasis in mammalian oocytes and eggs
AU - Wakai, Takuya
AU - Mehregan, Aujan
AU - Fissore, Rafael A.
N1 - Funding Information:
This work was supported by grants from the National Institutes of Health/National Institute of Child Health and Human Development (NIH/NICHD HD092499) and National Institute of Food and Agriculture/Hatch (NIFA/ Hatch) to R.A.F. We thank all members of the Fissore laboratory for their generous contributions and suggestions. We apologize to those whose work was not cited owing to space limitations
Publisher Copyright:
© 2019, Cold Spring Harbor Laboratory Press. All rights reserved.
PY - 2019/12
Y1 - 2019/12
N2 - Changes in the intracellular concentration of calcium ([Ca2+]i) represent a vital signaling mechanism enabling communication between and among cells as well as with the environment. Cells have developed a sophisticated set of molecules, “the Ca2+ toolkit,” to adapt [Ca2+]i changes to specific cellular functions. Mammalian oocytes and eggs, the subject of this review, are not an exception, and in fact the initiation of embryo devolvement in all species is entirely dependent on distinct [Ca2+]i responses. Here, we review the components of the Ca2+ toolkit present in mammalian oocytes and eggs, the regulatory mechanisms that allow these cells to accumulate Ca2+ in the endoplasmic reticulum, release it, and maintain basal and stable cytoplasmic concentrations. We also discuss electrophysiological and genetic studies that have uncovered Ca2+ influx channels in oocytes and eggs, and we analyze evidence supporting the role of a sperm-specific phospholipase C isoform as the trigger of Ca2+ oscillations during mammalian fertilization including its implication in fertility.
AB - Changes in the intracellular concentration of calcium ([Ca2+]i) represent a vital signaling mechanism enabling communication between and among cells as well as with the environment. Cells have developed a sophisticated set of molecules, “the Ca2+ toolkit,” to adapt [Ca2+]i changes to specific cellular functions. Mammalian oocytes and eggs, the subject of this review, are not an exception, and in fact the initiation of embryo devolvement in all species is entirely dependent on distinct [Ca2+]i responses. Here, we review the components of the Ca2+ toolkit present in mammalian oocytes and eggs, the regulatory mechanisms that allow these cells to accumulate Ca2+ in the endoplasmic reticulum, release it, and maintain basal and stable cytoplasmic concentrations. We also discuss electrophysiological and genetic studies that have uncovered Ca2+ influx channels in oocytes and eggs, and we analyze evidence supporting the role of a sperm-specific phospholipase C isoform as the trigger of Ca2+ oscillations during mammalian fertilization including its implication in fertility.
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U2 - 10.1101/cshperspect.a035162
DO - 10.1101/cshperspect.a035162
M3 - Article
C2 - 31427376
AN - SCOPUS:85075962091
SN - 1943-0264
VL - 11
JO - Cold Spring Harbor perspectives in biology
JF - Cold Spring Harbor perspectives in biology
IS - 12
M1 - a035162
ER -