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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.
Abstract:
Primordial follicle pool is the foundation of female reproductive life and abnormal primordial follicle activation may lead to severe diseases such as premature ovarian failure and premature ovarian insufficiency. Golgi reassembly stacking protein 2 (GORASP2) plays an important role in autophagy by regulating autophagy maturation through glycosylation modification. In the current study we found that GORASP2 is a key factor in mammalian primordial follicle activation through autophagy lysosome pathway. Knocking down of Gorasp2 in the ovaries of newborn mice led to decreased number of activated primary follicles, and the level of FSH (Follicle-stimulating Hormone) in the primary follicles was increased. Comparing with negative control ovaries, transcription profiling showed differentially expressed genes were mainly enriched in the autophagic lysosome, HIF-1 signaling pathway and PI3K-AKT signaling pathway. We found that the ratio of autophagy marker protein LC3-II/LC3-I increased and the level of SQSTM1 protein decreased by Western blot, indicating an elevated autophagy level in GORASP2-knockdown ovaries. Further examination demonstrated that the small G protein Rap1, a member of the Ras superfamily was activated after GORASP2 inhibition and the phosphorylation of mTOR was inhibited by disrupting the mTOR-Raptor interaction, thus initiating autophagy in primordial follicles. In addition, levels of ROS and ATP were increased and citrate lyase was decreased, suggesting a putative disrupted mitochondrial function. Finally, AKT signaling pathways were blocked and may also affect the developmental potential of these affected primordial follicles. In summary, our study emphasized the Golgi stacking protein GORASP2 as an important regulator in primordial follicle activation by participating in the initiation of autophagy, providing an experimental basis for the involvement of Golgi related components in the activation process of primordial follicles through autophagy pathway. This study also shed light upon the deeper understanding of primordial follicle activation related diseases and may contribute a new angle for their future treatment.
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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