The Golgi Stacking Protein GORASP2 Regulates Mouse Primordial Follicle Activation by Suppressing the Autophagy

Saifei Hu1, Yipin Wang1, Tian Wu1

  • 1State Key Laboratory of Reproduction Medicine and Offspring Health, Nanjing Medical University, Nanjing, Jiangsu, China.

Insights

Golgi reassembly stacking protein 2 (GORASP2) is crucial for activating primordial follicles in mammals. Inhibiting GORASP2 disrupts autophagy, affecting follicle development and potentially leading to ovarian insufficiency.

Area of Science:

  • Reproductive Biology
  • Cellular Biology
  • Molecular Endocrinology

Background:

  • The primordial follicle pool is vital for female fertility.
  • Aberrant primordial follicle activation is linked to premature ovarian failure and insufficiency.
  • Golgi reassembly stacking protein 2 (GORASP2) influences autophagy maturation via glycosylation.

Purpose of the Study:

  • To investigate the role of GORASP2 in mammalian primordial follicle activation.
  • To elucidate the mechanism by which GORASP2 regulates primordial follicle activation through the autophagy-lysosome pathway.

Main Methods:

  • Knockdown of Gorasp2 in newborn mouse ovaries.
  • Transcriptome profiling and Western blot analysis.
  • Analysis of autophagy markers, signaling pathways (HIF-1, PI3K-AKT), and mitochondrial function indicators (ROS, ATP, citrate lyase).

Main Results:

  • Gorasp2 knockdown decreased primary follicle activation and increased Follicle-stimulating Hormone (FSH) levels.
  • Gene expression changes indicated enrichment in autophagic lysosome, HIF-1, and PI3K-AKT pathways.
  • Elevated autophagy, Rap1 activation, mTOR inhibition, disrupted mitochondrial function, and blocked AKT signaling were observed.

Conclusions:

  • GORASP2 is a key regulator of primordial follicle activation, primarily through initiating autophagy.
  • The study provides evidence for Golgi components involvement in primordial follicle activation via autophagy.
  • Findings offer insights into diseases related to primordial follicle activation and potential therapeutic targets.

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