Regulation of [Ca2+]i oscillations and mitochondrial activity by various calcium transporters in mouse oocytes

Feng Wang1,2, Ang Li2, Tie-Gang Meng1,2

  • 1Fertility Preservation Lab, Reproductive Medicine Center, Guangdong Second Provincial General Hospital, Guangzhou, 510317, China.

Insights

Calcium channels like SERCAs, TRPM7, and T-type channels are crucial for regulating calcium oscillations during oocyte activation. This process is vital for mitochondrial function and embryo development, offering insights for fertility treatments.

Area of Science:

  • Reproductive Biology
  • Cell Physiology
  • Molecular Medicine

Background:

  • Oocyte activation inefficiency contributes to female infertility.
  • Intracellular calcium (Ca2+) dynamics are critical regulators of oocyte activation.

Purpose of the Study:

  • To investigate the roles of specific Ca2+ channels in regulating intracellular Ca2+ ([Ca2+]i) oscillations and mitochondrial membrane potential during oocyte activation.
  • To understand the impact of these channels on oocyte cytoskeleton stability and subsequent embryo development.

Main Methods:

  • Real-time recording of [Ca2+]i oscillations and mitochondrial membrane potential.
  • Utilized inhibitors for sarcoplasmic/endoplasmic reticulum Ca2+ATPases (SERCAs), transient receptor potential (TRP) ion channel subfamily member 7 (TRPM7), T-type Ca2+ channels, and calcium channel Orai1.

Main Results:

  • SERCAs, TRPM7, and T-type Ca2+ channels are essential for initiating and maintaining [Ca2+]i oscillations.
  • These oscillations are necessary for mitochondrial membrane potential elevation, oocyte cytoskeleton stability, and successful embryo development.
  • Orai1's role was also investigated in the context of these processes.

Conclusions:

  • Specific Ca2+ transport mechanisms, including SERCAs, TRPM7, and T-type channels, play pivotal roles in oocyte activation.
  • Understanding calcium transport mechanisms provides a foundation for improving oocyte activation in assisted reproduction.
  • Targeting these channels could enhance fertility treatments.