Calcium influx and sperm-evoked calcium responses during oocyte maturation and egg activation

Ya-Ru Xu and Wan-Xi Yang _

PDF  |  HTML  |  How to cite

Oncotarget. 2017; 8:89375-89390. https://doi.org/10.18632/oncotarget.19679

Metrics: PDF 1643 views  |   HTML 3275 views  |   ?  


Ya-Ru Xu1 and Wan-Xi Yang1

1 The Sperm Laboratory, College of Life Sciences, Zhejiang University, Hangzhou, China

Correspondence to:

Wan-Xi Yang, email:

Keywords: oocyte maturation, calcium influx, egg activation, calcium oscillation, calcium response

Received: May 09, 2017 Accepted: June 19, 2017 Published: July 29, 2017


Under the guidance and regulation of hormone signaling, large majority of mammalian oocytes go through twice cell cycle arrest-resumption prior to the fertilized egg splits: oocyte maturation and egg activation. Cytosolic free calcium elevations and endoplasmic reticulum calcium store alternations are actively involved in triggering the complex machineries and events during oogenesis. Among these, calcium influx had been implicated in the replenishment of endoplasmic reticulum store during oocyte maturation and calcium oscillation during egg activation. This process also drove successful fertilization and early embryo development. Store-operated Ca2+ entry, acts as the principal force of calcium influx, is composed of STIM1 and Orai1 on the plasma membrane. Besides, transient receptor potential channels also participate in the process of calcium inwards. In this review, we summarize the recent researches on the spatial-temporal distribution of store-operated calcium entry components and transient receptor potential channels. Questions about how these channels play function for calcium influx and what impacts these channels have on oocytes are discussed. At the time of sperm-egg fusion, sperm-specific factor(s) diffuse and enable eggs to mount intracellular calcium oscillations. In this review, we also focus on the basic knowledge and the modes of action of the potential sperm factor phospholipase C zeta, as well as the downstream receptor, type 1 inositol 1,4,5-trisphosphate receptor. From the achievement in the previous several decades, it is easy to find that there are too many doubtful points in the field that need researchers take into consideration and take action in the future.

Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 4.0 License.
PII: 19679