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异质性核糖核蛋白A2B1通过m⁶A/溶质载体家族7成员11抑制早发性卵巢功能不全中的颗粒细胞铁死亡。

hnRNPA2B1 restrains granulosa cell ferroptosis by mA/SLC7A11 in premature ovarian failure.

作者信息

Xiong Jing, He Ling, Zhang Yongjing, Zhao Xing

机构信息

Department of Obstetrics and Gynecology, The Second Xiangya Hospital of Central South University, Changsha, 410011, Hunan, China.

出版信息

J Ovarian Res. 2025 Jul 26;18(1):165. doi: 10.1186/s13048-025-01718-y.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b4c/12297619/f4d02165d764/13048_2025_1718_Fig1_HTML.jpg

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