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Follicle is a primary structural and functional unit within the mammalian ovary, encompassing a centrally positioned oocyte surrounded by pregranulosa cells. Primordial follicles constitute the ovarian reserve, the activated primary follicle represents the inception of follicular development in mammals. The intricate balance between primordial follicle dormancy and activation is pivotal for sustaining ovarian reproductive function; over-activation of the primordial follicle pool can result in premature ovarian failure among women. Although recent studies have revealed that several functional genes and pathways, such as mammalian target of rapamycin signaling, play roles in controlling the activation of primordial follicles, our understanding of the molecular networks regulating the activation progress is still incomplete. Here, using the mouse in vitro ovarian culture model, we identify a new role for K (lysine) acetyltransferase 6 A (KAT6A) in regulating the activation of primordial follicles in mice. Our results show that the expression of KAT6A is increased during primordial follicle activation in the oocytes. Disruption of KAT6A activity with two specific inhibitors significantly suppresses primordial follicle activation in cultured mouse ovaries. Furthermore, we find that KAT6A regulates processing body (P-body) signaling pathway and the expression levels of in oocytes. This suggests that KAT6A may promote primordial follicle activation by regulating the P-body signaling pathway. Collectively, our results elucidate that KAT6A plays a crucial role in controlling the activation of primordial follicles in the mammalian ovary. The dynamic balance between primordial follicle dormancy and activation is important for the maintenance of ovarian reproductive function. Our results show that the expression of KAT6A is increased during primordial follicle activation in the oocytes. Using two inhibitors of KAT6A exhibited decreased speed of primordial follicles activation in cultured mouse ovaries, and expression was increased in oocytes. Collectively, our results reveal that KAT6A controls the activation of primordial follicles in the mammalian ovary.
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http://dx.doi.org/10.1152/ajpcell.00055.2025 | DOI Listing |
Mol Hum Reprod
September 2025
Department of Veterinary Sciences, Laboratory of Veterinary Physiology and Biochemistry, Gamete Research Centre, University of Antwerp, Antwerp, Belgium.
Maternal diet-induced obesity (DIO) may affect adult offspring oocyte quality due to mitochondrial dysfunction. Here, we investigated whether offspring of DIO mothers exhibit mitochondrial abnormalities in their primordial follicle oocytes (PFOs) already at birth, and if (further) alterations can be detected at weaning. Female Swiss mice were fed a control or obesogenic diet for 7 weeks before mating, and throughout pregnancy and lactation.
View Article and Find Full Text PDFEcotoxicol Environ Saf
September 2025
School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan 450001, China; Institute for biological therapy, Henan Academy of Innovations in Medical Science, Zhengzhou, Henan 451163, China. Electronic address:
Diethyl phthalates (DEP) are commonly used as a plasticizer and have been found to cause male reproductive defects and metabolic disease in mammals as a potential environmental endocrine disruptor. However, the effects and underlying mechanisms of DEP exposure on female follicle development and oocyte maturation were still unclear. In this study, we found that mice exposed to DEP had significantly reduced primordial follicles.
View Article and Find Full Text PDFFront Cell Dev Biol
August 2025
Reproductive Medicine Center, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Introduction: Several aquaporins (AQPs) are involved in the influx of water to form follicular fluid, and AQP2 may play a crucial role in follicular growth. However, the specific roles of Aquaporin (AQP) 2 and AQP6 in granulosa cells (GCs) during follicular fluid (FF) formation, as well as their relationship with gonadotropins (Gn), remain unclear.
Methods: Luteinized granulosa cells (LGCs) were isolated from follicles of different diameters.
Stem Cell Res Ther
September 2025
State Key Laboratory of Reproductive Medicine and Offspring Health, Nanjing Medical University, Nanjing, Jiangsu, China.
Background: Polycystic Ovary Syndrome (PCOS), is a complex endocrine disorder affecting 6-21% of reproductive-aged women, characterized by chronic anovulation, hyperandrogenism, and polycystic ovarian morphology. Current clinical management relies on lifestyle modifications and symptom-targeted therapies due to the absence of curative interventions. In recent years, Laparoscopic ovarian drilling (LOD), a surgical procedure that induces controlled ovarian damage to stimulate primordial follicle activation and regulate follicular growth, has emerged as an established therapeutic intervention for infertility in PCOS.
View Article and Find Full Text PDFTheriogenology
August 2025
Department of Anatomy, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, 10330, Thailand. Electronic address:
Growth differentiation factor 9 (GDF9), bone morphogenetic protein 15 (BMP15), and anti-Müllerian hormone (AMH), members of the transforming growth factor-beta (TGF-β) superfamily, play critical roles in follicular development and oocyte maturation and are utilized as prognostic markers of fertility. This study aims to investigate the expression patterns of GDF9, BMP15, and AMH in different follicular developmental stages and across distinct reproductive phases in the feline ovary. Feline ovaries (N = 24) were divided into four ovarian statuses: prepubertal (n = 6), follicular (n = 6), luteal (n = 6), and inactive (n = 6).
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