Magee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA.
Magee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA; Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, PA, USA.
Placenta. 2023 Nov;143:54-61. doi: 10.1016/j.placenta.2023.10.001. Epub 2023 Oct 6.
Opioid use disorder (OUD) is implicated in major obstetrical diseases such as fetal growth restriction. Whether or not opioids directly impact placental trophoblast development and function remains unclear. We sought to examine the expression of opioid receptors (OPRs) in villous trophoblasts and the effect of opioids on placental transcriptomics.
Trophoblast stem (TS) cells and primary human trophoblast (PHT) cells from healthy term placentas were used to assess OPR expression in conditions that enhance trophoblast stemness vs differentiation. Placental RNAseq was conducted using our retrospective cohorts of pregnant people with OUD vs controls, both without major obstetrical complications. RT-qPCR was used to determine the effect of fentanyl on the expression of putative opioid targets and stemness or differentiation-associated genes in TS and PHT cells.
Three main OPRs, including OPRM1, OPRD1, and OPRK1 were expressed in term PHT cells cultured in the stemness medium, whereas only OPRD1 and OPRK1 were expressed in TS cells. Interestingly, upon induction of differentiation, the expressed OPR mRNAs in TS or in PHT cells were downregulated. We found 286 differentially expressed long RNAs in placentas from the OUD participants vs controls. While three putative opioid targets differed their expression in stemness vs differentiation states of trophoblasts, fentanyl had no effect on their expression or the expression of major stemness or differentiation-relevant genes in TS and PHT cells.
Trophoblastic expression of OPRs and opioid RNA targets is impacted by cell differentiation, suggesting differential susceptibility of villous trophoblasts to the effect of opioids.
阿片类药物使用障碍(OUD)与胎儿生长受限等主要产科疾病有关。阿片类药物是否直接影响胎盘滋养层的发育和功能尚不清楚。我们试图研究阿片受体(OPR)在绒毛滋养层中的表达,以及阿片类药物对胎盘转录组的影响。
使用来自健康足月胎盘的滋养层干细胞(TS)细胞和原代人滋养层(PHT)细胞,在增强滋养层干细胞特性与分化的条件下评估 OPR 表达。使用我们的回顾性队列,对患有 OUD 和对照组的孕妇进行胎盘 RNAseq 检测,两组均无主要产科并发症。使用 RT-qPCR 确定芬太尼对 TS 和 PHT 细胞中假定的阿片类药物靶基因和干细胞或分化相关基因表达的影响。
在培养于干细胞培养基中的足月 PHT 细胞中表达了三种主要的 OPR,包括 OPRM1、OPRD1 和 OPRK1,而在 TS 细胞中仅表达了 OPRD1 和 OPRK1。有趣的是,在诱导分化时,TS 或 PHT 细胞中表达的 OPR mRNA 下调。我们在 OUD 参与者和对照组的胎盘组织中发现了 286 个差异表达的长 RNA。虽然三个假定的阿片类药物靶基因在滋养层的干细胞特性与分化状态中的表达不同,但芬太尼对其表达或 TS 和 PHT 细胞中主要干细胞或分化相关基因的表达没有影响。
滋养层中 OPR 和阿片类药物 RNA 靶基因的表达受细胞分化的影响,这表明绒毛滋养层对阿片类药物的作用存在不同的敏感性。