Zhu Haibin, Ren Qianlei, Yan Ziyi, Xu Shouying, Luo Jiahao, Wu Ximei, Tang Chao
National Clinical Research Center for Child Health of the Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310052, China; Department of Obstetrics and Gynaecology, The First Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang 310003, China.
National Clinical Research Center for Child Health of the Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310052, China; Department of Pharmacology, School of Medicine, Zhejiang University, Hangzhou, Zhejiang 310058, China.
J Genet Genomics. 2022 Apr;49(4):350-363. doi: 10.1016/j.jgg.2021.07.014. Epub 2021 Aug 12.
Steroidogenesis from cholesterol in placental trophoblasts is fundamentally involved in the establishment and maintenance of pregnancy. The transcription factor gene heart and neural crest derivatives expressed 1 (Hand1) promotes differentiation of mouse trophoblast giant cells. However, the role of HAND1 in human trophoblasts remains unknown. Here, we report that HAND1 inhibits human trophoblastic progesterone (P4) and estradiol (E2) from cholesterol through downregulation of the expression of steroidogenic enzymes, including aromatase, P450 cholesterol side-chain cleavage enzyme (P450scc), and 3β-hydroxysteroid dehydrogenase type 1 (3β-HSD1). Mechanically, although HAND1 inhibits transcription of aromatase by directly binding to aromatase gene promoter, it restrains transcription of P450scc by upregulation of the methylation status of P450scc gene promoter through its binding to ALKBH1, a demethylase. Unlike aromatase and P450scc, HAND1 decreases 3β-HSD1 mRNA levels by the reduction of its RNA stability through binding to and subsequent destabilizing protein HuR. Finally, HAND1 suppresses circulating P4 and E2 levels derived from JEG-3 xenograft and attenuates uterine response to P4 and E2. Thus, our results uncover a hitherto uncharacterized role of HAND1 in the regulation of cholesterol metabolism in human trophoblasts, which may help pinpoint the underlying mechanisms involved in supporting the development and physiological function of the human placenta.
胎盘滋养层细胞中由胆固醇生成类固醇激素的过程在妊娠的建立和维持中起着根本性作用。转录因子基因心脏和神经嵴衍生物表达1(HAND1)促进小鼠滋养层巨细胞的分化。然而,HAND1在人滋养层细胞中的作用仍不清楚。在此,我们报告HAND1通过下调包括芳香化酶、细胞色素P450胆固醇侧链裂解酶(P450scc)和1型3β-羟基类固醇脱氢酶(3β-HSD1)在内的类固醇生成酶的表达,抑制人滋养层细胞从胆固醇生成孕酮(P4)和雌二醇(E2)。在机制上,虽然HAND1通过直接结合芳香化酶基因启动子来抑制芳香化酶的转录,但它通过与去甲基化酶ALKBH1结合,上调P450scc基因启动子的甲基化状态,从而抑制P450scc的转录。与芳香化酶和P450scc不同,HAND1通过与不稳定蛋白HuR结合并使其失稳,降低其RNA稳定性,从而降低3β-HSD1的mRNA水平。最后,HAND1抑制源自JEG-3异种移植的循环P4和E2水平,并减弱子宫对P4和E2的反应。因此,我们的结果揭示了HAND1在调节人滋养层细胞胆固醇代谢中迄今未被描述的作用,这可能有助于查明支持人胎盘发育和生理功能的潜在机制。