Journal Article

P62 promotes FSH-induced antral follicle formation by directing degradation of ubiquitinated WT1

Qin, Shaogang, Wang, Fengchao, Chen, Ziqi, Zheng, Wenying, Gao, Meng, Zhang, Hua, Liu, Longping, Wang, Haibin, Wang, Jianbin, Zhang, Tuo, Zhou, Bo, Wang, Chao, Xia, Guoliang, Zhao, Ting, Zhu, Zijian, Han, Jun, He, Meina, Wang, Wenji

2024

Overview

In females, the pathophysiological mechanism of poor ovarian response (POR) is not fully understood. Considering the expression level of p62 was significantly reduced in the granulosa cells (GCs) of POR patients, this study focused on identifying the role of the selective autophagy receptor p62 in conducting the effect of follicle-stimulating hormone (FSH) on antral follicles (AFs) formation in female mice. The results showed that p62 in GCs was FSH responsive and that its level increased to a peak and then decreased time-dependently either in ovaries or in GCs after gonadotropin induction in vivo. GC-specific deletion of p62 resulted in subfertility, a significantly reduced number of AFs and irregular estrous cycles, which were same as pathophysiological symptom of POR. By conducting mass spectrum analysis, we found the ubiquitination of proteins was decreased, and autophagic flux was blocked in GCs. Specifically, the level of nonubiquitinated Wilms tumor 1 homolog (WT1), a transcription factor and negative controller of GC differentiation, increased steadily. Co-IP results showed that p62 deletion increased the level of ubiquitin-specific peptidase 5 (USP5), which blocked the ubiquitination of WT1. Furthermore, a joint analysis of RNA-seq and the spatial transcriptome sequencing data showed the expression of steroid metabolic genes and FSH receptors pivotal for GCs differentiation decreased unanimously. Accordingly, the accumulation of WT1 in GCs deficient of p62 decreased steroid hormone levels and reduced FSH responsiveness, while the availability of p62 in GCs simultaneously ensured the degradation of WT1 through the ubiquitin‒proteasome system and autophagolysosomal system. Therefore, p62 in GCs participates in GC differentiation and AF formation in FSH induction by dynamically controlling the degradation of WT1. The findings of the study contributes to further study the pathology of POR.

• Publisher: Springer International Publishing,Springer Nature B.V
• Subject: Animals / Apoptosis / Autophagy / Autophagy - drug effects / Biochemistry / Biomedical and Life Sciences / Biomedicine / Cell Biology / Cell cycle / Degradation / Deletion / Differentiation / Female / Females / Fertility / Follicle Stimulating Hormone - metabolism / Follicle Stimulating Hormone - pharmacology / Follicle-stimulating hormone / Follicles / Gene expression / Gene sequencing / Gonadotropins / Granulosa cells / Granulosa Cells - drug effects / Granulosa Cells - metabolism / Hormones / Humans / Life Sciences / Mice / Mice, Inbred C57BL / Mice, Knockout / neoplasms / Original / Original Article / Ovarian Follicle - drug effects / Ovarian Follicle - metabolism / ovarian follicles / Ovaries / Peptides / Pituitary (anterior) / Pregnancy / Proteasomes / Proteins / Proteolysis - drug effects / Receptors / sequence analysis / Sequestosome-1 Protein - genetics / Sequestosome-1 Protein - metabolism / Spectrum analysis / steroid hormones / Steroids / Transcription factors / transcriptome / Transcriptomes / Ubiquitin / Ubiquitination / Womens health / WT1 protein / WT1 Proteins - genetics / WT1 Proteins - metabolism