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HUWE1通过泛素化介导的WT1降解参与支持细胞极性的建立。

HUWE1 is involved in Sertoli cell polarity establishment by ubiquitination mediated degradation of WT1.

作者信息

Liu Bowen, Wang Mengyue, Cen Changhuo, Shen Zhiming, Li Jiayi, Cui Xiuhong, Zhao Xudong, Chen Min, Gao Fei

机构信息

State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.

Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing, China.

出版信息

Cell Mol Life Sci. 2025 Jul 3;82(1):271. doi: 10.1007/s00018-025-05779-6.

Abstract

HUWE1, a member of HECT E3 ubiquitin ligase family, is implicated in a variety of cellular processes. Recent studies find that HUWE1 also plays critical roles in germ cell development and inactivation of HUWE1 causes germ cell loss in both male and female mice. In this study, we found that Huwe1 was also highly expressed in testicular Sertoli cells. Inactivation of Huwe1 in Sertoli cells resulted in loss of cell polarity, which in turn caused germ cells loss and male infertility. Further study revealed that dysregulation in the expression of cytoskeletal and adhesion-related molecules, as well as a significant increase in EMT-related trans-factors SNAI1&2 in Huwe1-deficient Sertoli cells. Intriguingly, the protein level of WT1 was significantly increased in Huwe1-deficient Sertoli cells, and overexpression of Wt1 in Sertoli cells also caused the defects in spermatogenesis which was consistent with Huwe1 CKO mouse model. Furthermore, the defect of spermatogenesis in Huwe1 CKO mice was partially rescued by deleting one allele of Wt1 gene. Mechanistic studies revealed that WT1 interacts with HUWE1 protein and it could be ubiquitinated by HUWE1. Our study demonstrates that HUWE1 is involved in the establishment of Sertoli cell polarity mainly by regulating the protein level of WT1 gene.

摘要

HUWE1是HECT E3泛素连接酶家族的成员之一,参与多种细胞过程。最近的研究发现,HUWE1在生殖细胞发育中也起着关键作用,HUWE1的失活会导致雄性和雌性小鼠的生殖细胞丢失。在本研究中,我们发现Huwe1在睾丸支持细胞中也高度表达。支持细胞中Huwe1的失活导致细胞极性丧失,进而导致生殖细胞丢失和雄性不育。进一步研究表明,细胞骨架和黏附相关分子的表达失调,以及Huwe1缺陷型支持细胞中EMT相关转录因子SNAI1和SNAI2显著增加。有趣的是,WT1的蛋白水平在Huwe1缺陷型支持细胞中显著升高,在支持细胞中过表达Wt1也会导致精子发生缺陷,这与Huwe1基因敲除小鼠模型一致。此外,通过删除Wt1基因的一个等位基因,部分挽救了Huwe1基因敲除小鼠的精子发生缺陷。机制研究表明,WT1与HUWE1蛋白相互作用,并且可以被HUWE1泛素化。我们的研究表明,HUWE1主要通过调节WT1基因的蛋白水平参与支持细胞极性的建立。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20cc/12226439/e4c0e2c2fb0c/18_2025_5779_Fig1_HTML.jpg

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