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Updated: Dec 11, 2025

In Vivo Visualization of Calcium Transients during Fertilization and Early Development in C. elegans
Published on: July 12, 2024
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.
Abstract:
Oocyte activation inefficiency is one of the reasons for female infertility and Ca2+ functions play a critical role in the regulation of oocyte activation. We used various inhibitors of Ca2+ channels located on the membrane, including sarcoplasmic/ endoplasmic reticulum Ca2+ATPases (SERCAs, the main Ca2+ pumps which decrease the intracellular Ca2+ level by refilling Ca2+ into the sarcoplasmic reticulum), transient receptor potential (TRP) ion channel subfamily member 7 (TRPM7, a Ca2+/Mg2+-permeable non-selective cation channel), T-type Ca2+ channels and calcium channel Orai1, to investigate their roles in [Ca2+]i oscillation patterns and mitochondrial membrane potential during oocyte activation by real-time recording. Our results showed that SERCAs, TRPM7 and T-type Ca2+ channels were important for initiation and maintenance of [Ca2+]i oscillations, which was required for mitochondrial membrane potential elevation during oocyte activation, as well as oocyte cytoskeleton stability and subsequent embryo development. Increasing the knowledge of calcium transport may provide a theoretical basis for improving oocyte activation in human assisted reproduction clinics.
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.
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