Li Dong, Duan Honglei, Jiang Zihan, Zhou Chunxiang, Cao Chenrui, Ni Mengyao, He Linlin, Zhu Xiangyu, Jin Liang, Liu Wei, Gu Leilei, Li Huijun, Liu Dan, Zhao Xiaolei, Zhao Guangfeng, Li Jie
Department of Obstetrics and Gynecology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, 210000, Nanjing, China.
Department of Obstetrics and Gynecology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, 210000, Nanjing, China.
Free Radic Biol Med. 2025 Sep;237:270-284. doi: 10.1016/j.freeradbiomed.2025.06.003. Epub 2025 Jun 4.
The survival of decidual stromal cells (DSCs) at the maternal-fetal interface is critical for maintaining pregnancy. Dysfunction of DSCs is a significant contributor to recurrent spontaneous abortion (RSA), though the precise regulatory mechanisms remain elusive. Here, we report a marked downregulation of fatty acid-binding protein 5 (FABP5) in decidual tissues and DSCs from RSA donors, suggesting its potential role in RSA pathogenesis.
Using decidual tissues and DSCs from normal pregnancy (NP) and RSA donors, we quantified FABP5 expression via qPCR, Western blot, immunofluorescence, and immunohistochemistry. Cellular viability and apoptosis were assessed through CCK8 assays, Ki67 staining, flow cytometry, and TUNEL assays. Mitochondrial integrity and function were evaluated by JC-1 staining, COXIV immunostaining, and ATP quantification. RNA sequencing (RNA-seq) identified downstream targets of FABP5. The migratory and invasive capacities of human extravillous trophoblast cells line (HTR-8/SVneo) were examined via wound healing and transwell assays.
FABP5 expression was significantly reduced in decidual tissues and DSCs from RSA donors, as well as in tert-butyl hydroperoxide (TBHP)-induced oxidative stress models in vitro. siRNA-mediated FABP5 knockdown triggered mitochondrial dysfunction and apoptosis in DSCs, mechanistically linked to mitochondrial ribosomal protein L17 (MRPL17), a pivotal regulator of oxidative respiratory chain enzyme complex synthesis. MRPL17 overexpression alleviated these effects. Furthermore, FABP5 deficiency suppressed CXCL11 secretion, leading to diminished CXCR3 levels in HTR-8/SVneo cells and impairing their migration and invasion.
Our findings demonstrate that FABP5 downregulation compromises DSC survival by disrupting MRPL17-dependent mitochondrial function, thereby attenuating CXCL11/CXCR3 mediated trophoblast invasion and migration. This study unveils a novel FABP5/MRPL17/CXCL11/CXCR3 axis in RSA pathogenesis, highlighting FABP5 as a potential therapeutic target for pregnancy maintenance.
蜕膜基质细胞(DSCs)在母胎界面的存活对于维持妊娠至关重要。DSCs功能障碍是复发性自然流产(RSA)的一个重要因素,尽管其确切的调控机制仍不清楚。在此,我们报告了RSA供体的蜕膜组织和DSCs中脂肪酸结合蛋白5(FABP5)显著下调,提示其在RSA发病机制中的潜在作用。
使用来自正常妊娠(NP)和RSA供体的蜕膜组织和DSCs,我们通过qPCR、蛋白质免疫印迹、免疫荧光和免疫组织化学定量FABP5表达。通过CCK8检测、Ki67染色、流式细胞术和TUNEL检测评估细胞活力和凋亡。通过JC-1染色、COXIV免疫染色和ATP定量评估线粒体完整性和功能。RNA测序(RNA-seq)确定FABP5的下游靶点。通过伤口愈合和transwell检测检测人绒毛外滋养层细胞系(HTR-8/SVneo)的迁移和侵袭能力。
RSA供体的蜕膜组织和DSCs以及体外叔丁基过氧化氢(TBHP)诱导的氧化应激模型中FABP5表达显著降低。siRNA介导的FABP5敲低引发DSCs中的线粒体功能障碍和凋亡,其机制与线粒体核糖体蛋白L17(MRPL17)有关,MRPL17是氧化呼吸链酶复合物合成的关键调节因子。MRPL17过表达减轻了这些影响。此外,FABP5缺乏抑制CXCL11分泌,导致HTR-8/SVneo细胞中CXCR3水平降低,并损害其迁移和侵袭。
我们的研究结果表明,FABP5下调通过破坏依赖MRPL17的线粒体功能损害DSC存活,从而减弱CXCL11/CXCR3介导的滋养层侵袭和迁移。本研究揭示了RSA发病机制中一个新的FABP5/MRPL17/CXCL11/CXCR3轴,突出了FABP5作为维持妊娠的潜在治疗靶点。