PKCδ and θ possibly mediate FSH-induced mouse oocyte maturation via NOX-ROS-TACE cascade signaling pathway

Qian Chen1, Wenqiang Zhang1, Hao Ran1

  • 1State Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural University, Beijing, People's Republic of China.

Plos One
|October 29, 2014
PubMed

Insights

Protein kinase C delta and theta (PKCδ/θ) mediate FSH-induced mouse oocyte maturation. This occurs through the nicotinamide adenine dinucleotide phosphate oxidase (NOX)-reactive oxygen species (ROS)-tumor necrosis factor-α converting enzyme (TACE) pathway.

Area of Science:

  • Reproductive Biology
  • Cell Signaling
  • Mammalian Oogenesis

Background:

  • Gonadotropins, like follicle-stimulating hormone (FSH), trigger oocyte maturation in mammals.
  • The epidermal growth factor (EGF) network and protein kinase C (PKC) signaling pathway are crucial mediators.
  • The precise signaling cascade linking PKC to tumor necrosis factor-α converting enzyme (TACE) in FSH-induced oocyte maturation is not fully understood.

Purpose of the Study:

  • To elucidate the signaling pathway between PKC and TACE in FSH-induced mouse oocyte maturation.
  • To investigate the role of PKCδ and PKCθ in this process.
  • To identify downstream effectors of PKC involved in mediating oocyte maturation.

Main Methods:

  • Used rottlerin (MTX), a PKCδ/θ inhibitor, to assess its effect on FSH-induced maturation of mouse cumulus-oocyte complexes (COCs).
  • Investigated the involvement of nicotinamide adenine dinucleotide phosphate oxidase (NOX) and reactive oxygen species (ROS) using specific inhibitors.
  • Examined the activity and translocation of NOX components (p47phox, p67phox) and TACE in response to FSH and PKC inhibition.
  • Assessed the partial rescue effect of amphiregulin (Areg) on inhibitory treatments.

Main Results:

  • Rottlerin (MTX) inhibited FSH-induced maturation of mouse COCs.
  • Inhibitors of NOX, ROS, and TACE dose-dependently blocked FSH-stimulated oocyte maturation, with partial reversal by Areg.
  • PKCδ/θ inhibition prevented FSH-induced translocation of p47phox and p67phox to the plasma membrane in cumulus cells.
  • NOX and ROS inhibition significantly decreased FSH-induced TACE activity.

Conclusions:

  • PKCδ and PKCθ are essential for FSH-induced meiotic resumption in mouse COCs.
  • The NOX-ROS-TACE signaling pathway is a likely downstream mediator of PKCδ/θ action.
  • This pathway plays a critical role in regulating oocyte maturation in response to FSH stimulation.