Shukla Vinay, Iqbal Khursheed, Okae Hiroaki, Arima Takahiro, Soares Michael J
Institute for Reproductive and Developmental Sciences, University of Kansas Medical Center, Kansas City, KS, USA.
Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS, USA.
Hum Reprod. 2025 Jun 1;40(6):1163-1172. doi: 10.1093/humrep/deaf075.
How does activation of aryl hydrocarbon receptor (AHR) signaling affect human trophoblast cell development and differentiation?
AHR activation alters gene expression without impairing the ability of trophoblast cells to maintain a stem cell state or differentiate into essential cell types, such as extravillous trophoblast (EVT) cells or syncytiotrophoblast (ST), while promoting the production of 2-methoxy estradiol (2ME), which may impact placental development.
The placenta serves both as a nutrient delivery system and a protective barrier against environmental toxins. AHR signaling is known to mediate cellular responses to environmental pollutants, potentially affecting trophoblast cell function, but the specific impacts of AHR activation on these cells were not fully understood.
STUDY DESIGN, SIZE, DURATION: This study utilized an in vitro model of human trophoblast stem (TS) cells to investigate the downstream effects of AHR activation. The study focused on both undifferentiated TS cells and cells undergoing differentiation.
PARTICIPANTS/MATERIALS, SETTING, METHODS: Human TS cells were used as a model system. Researchers examined the effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) exposure in TS cells maintained in their stem state and in TS cells induced to differentiate into EVT cells or ST. The study assessed changes in gene expression, particularly focusing on CYP1A1 and CYP1B1, as well as the production of 2ME.
AHR activation stimulated the expression of CYP1A1 and CYP1B1, key genes associated with AHR signaling, in both undifferentiated and differentiating trophoblast cells. While AHR activation did not impact the ability of the cell to remain in a stem state or differentiate, it increased the production of 2ME, which may influence placentation. These effects were dependent on AHR signaling.
n/a.
LIMITATIONS, REASONS FOR CAUTION: This study was conducted in vitro, which may not fully replicate in vivo conditions. Further research is needed to confirm whether these findings apply to placental development in humans.
The results suggest that AHR signaling activated by environmental pollutants could have a significant impact on placental development through mechanisms involving AHR activation. These findings may have broader implications for understanding how environmental factors affect fetal development.
STUDY FUNDING/COMPETING INTEREST(S): This work was funded by the National Institutes of Health: ES028957, HD020676, ES029280, HD105734, HD112559, and the Sosland Foundation. The authors declare no conflicts of interest.
芳烃受体(AHR)信号通路的激活如何影响人滋养层细胞的发育和分化?
AHR激活会改变基因表达,同时不会损害滋养层细胞维持干细胞状态或分化为重要细胞类型(如绒毛外滋养层细胞或合体滋养层细胞)的能力,还会促进2-甲氧基雌二醇(2ME)的产生,这可能会影响胎盘发育。
胎盘既是营养物质输送系统,也是抵御环境毒素的保护屏障。已知AHR信号通路可介导细胞对环境污染物的反应,可能影响滋养层细胞功能,但AHR激活对这些细胞的具体影响尚不完全清楚。
研究设计、规模、持续时间:本研究利用人滋养层干细胞(TS)的体外模型来研究AHR激活的下游效应。该研究聚焦于未分化的TS细胞和正在分化的细胞。
研究对象/材料、研究环境、方法:使用人TS细胞作为模型系统。研究人员检测了在维持干细胞状态的TS细胞以及诱导分化为绒毛外滋养层细胞或合体滋养层细胞的TS细胞中,2,3,7,8-四氯二苯并对二恶英(TCDD)暴露的影响。该研究评估了基因表达的变化,尤其关注细胞色素P450 1A1(CYP1A1)和细胞色素P450 1B1(CYP1B1),以及2ME的产生。
AHR激活在未分化和正在分化的滋养层细胞中均刺激了与AHR信号通路相关的关键基因CYP1A1和CYP1B1的表达。虽然AHR激活不影响细胞维持干细胞状态或分化的能力,但它增加了2ME的产生,这可能会影响胎盘形成。这些效应依赖于AHR信号通路。
无。
局限性、需谨慎的原因:本研究是在体外进行的,可能无法完全复制体内情况。需要进一步研究以确认这些发现是否适用于人类胎盘发育。
结果表明,环境污染物激活的AHR信号通路可能通过涉及AHR激活的机制对胎盘发育产生重大影响。这些发现可能对理解环境因素如何影响胎儿发育具有更广泛的意义。
研究资金/利益冲突:本研究由美国国立卫生研究院资助:ES028957、HD020676、ES029280、HD105734、HD112559以及索斯兰基金会。作者声明无利益冲突。