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脐带间充质干细胞来源的细胞外囊泡通过……改善颗粒细胞的过度自噬。

Umbilical cord mesenchymal stem cell-derived extracellular vesicles improve excessive autophagy of granulosa cells through .

作者信息

Zhou Weiqin, Zhang Ju, Lu Xuanping, Zhao Ziwei, Weng Yujing, Zhu Chunrong

机构信息

Reproductive Medicine Center, The First Affiliated Hospital of Soochow University, Suzhou, People's Republic of China.

Department of Gynaecology and Obstetrics, The First Affiliated Hospital of Soochow University, Suzhou, People's Republic of China.

出版信息

Am J Physiol Cell Physiol. 2025 May 1;328(5):C1586-C1604. doi: 10.1152/ajpcell.00785.2024. Epub 2025 Mar 19.

Abstract

Polycystic ovary syndrome (PCOS) is a prevalent endocrine disorder impacting women's fertility. We assessed the effect of umbilical cord mesenchymal stem cell-derived extracellular vesicles (UC-MSC-EVs) on PTEN-induced kinase 1 ()/-mediated excessive autophagy of ovarian granulosa cells (GCs) through methyltransferase-like 3 (). Human ovarian GC line KGN was cultured and treated with dehydroepiandrosterone (DHEA) and UC-MSC-EVs. Cell apoptosis and viability, autophagy-related protein levels, adenosine triphosphate (ATP) and mitochondrial membrane potential (MMP) level, and microtubule-associated protein 1 light chain 3 β (LC3B) and translocase of outer mitochondrial membrane 20 (TOMM20) colocalization were assessed by flow cytometry, CCK-8, Western blot, kit, and immunofluorescence. N6-methyladenosine (m6A) modification, levels, and mRNA stability were determined by methylated RNA immunoprecipitation, reverse transcription quantitative polymerase chain reaction, and Western blot. The PCOS mouse model was established and treated with UC-MSC-EVs. Serum hormone and ovarian tissue autophagy-related protein levels were determined by enzyme-linked immunosorbent assay. DHEA decreased KGN cell viability and p62 level, increased , , LC3BII/I, and Beclin-1 protein levels, ATP content, MMP level, TOMM20LC3B cell number, and apoptosis, which were partly abrogated by UC-MSC-EV treatment. PINK1 had m6A modification sites. METTL3 was a m6A-modified writer protein. After DHEA treatment, KGN cells showed elevated and m6A modification levels and mRNA stability, whereas UC-MSC-EV treatment caused the opposite results. METTL3 overexpression partly averted UC-MSC-EVs-improved /-mediated mitophagy. UC-MSC-EVs curbed PINK1/Parkin-mediated excessive autophagy through and improved ovarian function in PCOS mice. In conclusion, UC-MSC-EVs suppressed PINK1/Parkin-mediated mitophagy of ovarian GCs through METTL3, thereby improving PCOS. Polycystic ovary syndrome (PCOS) is a prevalent endocrine disorder impacting women's fertility. The authors in this study using DHEA-induced granulosa cells (GCs) demonstrated that umbilical cord mesenchymal stem cell-derived extracellular vesicles (UC-MSC-EVs) suppressed /-mediated mitophagy of ovarian GCs through METTL3, thereby improving PCOS.

摘要

多囊卵巢综合征(PCOS)是一种影响女性生育能力的常见内分泌疾病。我们评估了脐带间充质干细胞衍生的细胞外囊泡(UC-MSC-EVs)通过甲基转移酶样3(METTL3)对PTEN诱导激酶1(PINK1)/Parkin介导的卵巢颗粒细胞(GCs)过度自噬的影响。培养人卵巢GC系KGN并用脱氢表雄酮(DHEA)和UC-MSC-EVs处理。通过流式细胞术、CCK-8、蛋白质免疫印迹法、试剂盒和免疫荧光评估细胞凋亡和活力、自噬相关蛋白水平、三磷酸腺苷(ATP)和线粒体膜电位(MMP)水平以及微管相关蛋白1轻链3β(LC3B)和外线粒体膜转位酶20(TOMM20)的共定位。通过甲基化RNA免疫沉淀、逆转录定量聚合酶链反应和蛋白质免疫印迹法测定N6-甲基腺苷(m6A)修饰、METTL3水平和PINK1 mRNA稳定性。建立PCOS小鼠模型并用UC-MSC-EVs处理。通过酶联免疫吸附测定法测定血清激素和卵巢组织自噬相关蛋白水平。DHEA降低了KGN细胞活力和p62水平,增加了PINK1、Parkin、LC3BII/I和Beclin-1蛋白水平、ATP含量、MMP水平、TOMM20-LC3B细胞数量和细胞凋亡,而UC-MSC-EV处理部分消除了这些影响。PINK1有m6A修饰位点。METTL3是一种m6A修饰的书写蛋白。DHEA处理后,KGN细胞显示出m6A修饰水平和PINK1 mRNA稳定性升高,而UC-MSC-EV处理则产生相反的结果。METTL3过表达部分避免了UC-MSC-EVs改善的PINK1/Parkin介导的线粒体自噬。UC-MSC-EVs通过METTL3抑制PINK1/Parkin介导的卵巢GCs过度自噬,并改善PCOS小鼠的卵巢功能。总之,UC-MSC-EVs通过METTL3抑制PINK1/Parkin介导的卵巢GCs线粒体自噬,从而改善PCOS。多囊卵巢综合征(PCOS)是一种影响女性生育能力的常见内分泌疾病。本研究中使用DHEA诱导颗粒细胞(GCs)的作者证明,脐带间充质干细胞衍生的细胞外囊泡(UC-MSC-EVs)通过METTL3抑制PINK1/Parkin介导的卵巢GCs线粒体自噬,从而改善PCOS。

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