Xiong Jing, He Ling, Zhang Yongjing, Zhao Xing
Department of Obstetrics and Gynecology, The Second Xiangya Hospital of Central South University, Changsha, 410011, Hunan, China.
J Ovarian Res. 2025 Jul 26;18(1):165. doi: 10.1186/s13048-025-01718-y.
Premature ovarian failure (POF) is a relatively severe gynecological disorder that is often accompanied by other systemic diseases. Here, this study identified that N-methyladenosine (mA) key enzyme heterogeneous nuclear ribonucleoprotein A2/B1 (hnRNPA2B1) was associated with POF pathophysiological process. In the chemotherapy induced POF animal and cells, hnRNPA2B1 was down-regulated upon cisplatin (CDDP) treatment. Functionally, hnRNPA2B1 inhibited the ferroptosis phenotype by mA/SLC7A11 of granulosa cells. Moreover, hnRNPA2B1 up-regulated the autophagy by inhibiting PI3K/AKT/mTOR pathway of granulosa cells. Besides, rescue experiments confirmed that hnRNPA2B1/SLC7A11 axis repressed the ferroptosis of granulosa cells through mA-dependent manner. In summary, the research identified the critical role of hnRNPA2B1 in granulosa cells ferroptosis, which provides novel insight for POF treatment.
卵巢早衰(POF)是一种相对严重的妇科疾病,常伴有其他全身性疾病。在此,本研究发现N-甲基腺苷(mA)关键酶异质核糖核蛋白A2/B1(hnRNPA2B1)与POF的病理生理过程相关。在化疗诱导的POF动物和细胞中,顺铂(CDDP)处理后hnRNPA2B1表达下调。在功能上,hnRNPA2B1通过颗粒细胞的mA/SLC7A11抑制铁死亡表型。此外,hnRNPA2B1通过抑制颗粒细胞的PI3K/AKT/mTOR途径上调自噬。此外,挽救实验证实hnRNPA2B1/SLC7A11轴通过mA依赖方式抑制颗粒细胞的铁死亡。总之,该研究确定了hnRNPA2B1在颗粒细胞铁死亡中的关键作用,为POF治疗提供了新的见解。