Department of Obstetrics, Gynecology, and Reproductive Sciences, Yale School of Medicine, New Haven, CT 06510, USA.
IVIRMA Global Research Alliance, IVIRMA New Jersey, Marlton, NJ 07920, USA.
Int J Mol Sci. 2024 Feb 3;25(3):1866. doi: 10.3390/ijms25031866.
Mitochondrial unfolded protein stress response (mtUPR) plays a critical role in regulating cellular and metabolic stress response and helps maintain protein homeostasis. Caseinolytic peptidase P (CLPP) is one of the key regulators of mtUPR and promotes unfolded protein degradation. Previous studies demonstrated that global deletion of resulted in female infertility, whereas no impairment was found in the mouse model with targeted deletion of in cumulus/granulosa cells. These results suggest the need to delineate the function of in oocytes. In this study, we aimed to further explore the role of mtUPR in female reproductive competence and senescence using a mouse model. Oocyte-specific targeted deletion of in mice resulted in female subfertility associated with metabolic and functional abnormalities in oocytes, thus highlighting the importance of CLPP-mediated protein homeostasis in oocyte competence and reproductive function.
线粒体未折叠蛋白应激反应 (mtUPR) 在调节细胞和代谢应激反应中起着关键作用,并有助于维持蛋白质的内稳态。蛋白酶体 P (CLPP) 是 mtUPR 的关键调节因子之一,可促进未折叠蛋白的降解。先前的研究表明, 全局缺失导致雌性不孕,而在卵丘/颗粒细胞中靶向缺失 的小鼠模型中未发现损伤。这些结果表明需要阐明 在卵母细胞中的功能。在这项研究中,我们旨在使用小鼠模型进一步探索 mtUPR 在雌性生殖能力和衰老中的作用。在小鼠中卵母细胞特异性靶向敲除 导致雌性生育力降低,与卵母细胞中的代谢和功能异常有关,因此突出了 CLPP 介导的蛋白质内稳态在卵母细胞的能力和生殖功能中的重要性。