发病机制
流产
化学
双酚A
内分泌系统
泌尿系统
胎盘
转录因子
生物活性
内分泌学
医学
怀孕
细胞生物学
二羟基化合物
内科学
双酚S
流产
生物
细胞器
内分泌干扰物
男科
癌症研究
肠内分泌细胞
作者
Wenxin Huang,Manli Wang,Yi Sun,Xiao-Ping Yue,Xun Li,Yanbing Lin,Geng Guo,Depeng Zhao,Qigang Fan,Xiaoling Ma,Zhihong Zhang,Shuaishuai Xing,Xiaoting Shen,Huidong Zhang
标识
DOI:10.1002/advs.202504871
摘要
Abstract Unexplained miscarriage (UM) remains challenge due to unclear pathogenesis and biological mechanisms. BPB (Bisphenol B), an extensively used endocrine disrupting chemical, has been widely detected out in human. Migrasomes are newly identified cellular organelles with a large number of unknown functions. However, whether and how BPB exposure may suppress migrasome formation (MF) to induce miscarriage are completely unknown. In this study, it is found that higher urinary BPB levels are associated with the suppressed MF in villous tissues and unexplained miscarriage. It is further confirmed that BPB exposure suppresses MF in the mouse placenta and thus induces miscarriage. Supplement with Pkca or Tspan4, two essential proteins for migration/invasion (MI) and MF, can efficiently treat against BPB‐induced miscarriage. In biological mechanisms, BPB up‐regulates ER levels, enhances its interactions with the lnc‐HZ04 promoter region, and thus promotes ER‐mediated lnc‐HZ04 transcription. Subsequently, lnc‐HZ04 suppresses TCF4‐mediated PKCA transcription and subsequently suppresses MI and MF. Collectively, this study not only identifies BPB as a novel risk factor for unexplained miscarriage, discovers novel pathogenesis and biological mechanisms in BPB‐induced miscarriage, but also provides potential targets for treatment against unexplained miscarriage.
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