PAK4 Regulates Actin and Microtubule Dynamics during Meiotic Maturation in Mouse Oocyte

Ya-Ting He1, Lei-Lei Yang1, Shi-Ming Luo1

  • 1College of Animal Science and Technology, College of Life Sciences, Institute of Reproductive Science, Key Laboratory of Animal Reproduction and Germplasm Enhancement in Universities of Shandong, Qingdao Agricultural University, Qingdao 266109, China.

Insights

p-21 activated kinases (PAKs) regulate oocyte maturation and fertilization. Inhibiting PAK4 disrupts cytoskeleton dynamics, leading to meiotic arrest and aneuploidy, highlighting PAK4's crucial role in oocyte meiosis.

Area of Science:

  • Cell Biology
  • Reproductive Biology
  • Molecular Biology

Background:

  • Meiotic maturation of oocytes is essential for fertilization.
  • Cytoskeletal integrity plays a critical role in oocyte maturation.
  • p-21 activated kinases (PAKs) are serine/threonine kinases involved in cell motility, survival, cell cycle, and proliferation.

Purpose of the Study:

  • To investigate the function of PAK4 during mouse oocyte meiotic maturation.
  • To determine the effects of PAK4 inhibition on cytoskeletal dynamics and meiotic progression.

Main Methods:

  • Utilized a selective PAK4 inhibitor, PF-3758309, in mouse oocyte cultures.
  • Analyzed microfilament and microtubule dynamics.
  • Assessed kinetochore-microtubule (K-M) attachment and centrosome assembly.

Main Results:

  • PAK4 inhibition led to meiotic arrest.
  • Abnormal microfilament and microtubule dynamics were observed.
  • Impaired microtubule stability and defective K-M attachment resulted in aneuploidy.
  • Abnormal acentriolar centrosome assembly occurred during meiotic maturation.

Conclusions:

  • PAK4 is essential for successful oocyte meiotic maturation.
  • PAK4 regulates cytoskeleton dynamics, including microtubule stability and centrosome assembly.
  • PAK4 inhibition causes meiotic defects, emphasizing its role in ensuring proper chromosome segregation and fertilization potential.

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