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芳烃受体激活在人滋养层干细胞发育中驱动2-甲氧基雌二醇分泌。

Aryl Hydrocarbon Receptor Activation Drives 2-Methoxy Estradiol Secretion in Human Trophoblast Stem Cell Development.

作者信息

Shukla Vinay, Iqbal Khursheed, Okae Hiroaki, Arima Takahiro, Soares Michael J

机构信息

Institute for Reproductive and Developmental Sciences, University of Kansas Medical Center, Kansas City, KS 66160.

Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS 661602.

出版信息

bioRxiv. 2025 Jan 31:2024.08.27.609205. doi: 10.1101/2024.08.27.609205.

Abstract

STUDY QUESTION

How does activation of AHR signaling affect human trophoblast cell development and differentiation?

SUMMARY ANSWER

AHR activation leads to altered gene expression but does not hinder the ability of trophoblast cells to remain in a stem cell state or differentiate into essential cell types, such as extravillous trophoblast cells (EVT) or syncytiotrophoblast (ST). It also promotes the production of 2 methoxy estradiol (2ME), a compound that could influence placental development.

WHAT IS KNOWN ALREADY

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 functions, 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 trophoblast stem (TS) cells were used as the model system. Researchers examined the effects of TCDD exposure in both TS cells maintained in their stem state and those induced to differentiate into EVT or ST. The study assessed changes in gene expression, particularly focusing on and , as well as the production of 2ME.

MAIN RESULTS AND THE ROLE OF CHANCE

AHR activation stimulated the expression of and , key genes associated with AHR signaling, in both undifferentiated and differentiating trophoblast cells. While AHR activation did not impact the cells ability to remain in a stem state or differentiate, it increased the production of 2ME, which may influence placental function. These effects were dependent on AHR signaling.

LIMITATIONS REASONS FOR CAUTION

This study was conducted in vitro, which may not fully replicate human conditions. Further research is needed to confirm whether these findings apply to actual placental development in humans.

WIDER IMPLICATIONS OF THE FINDINGS

The results suggest that AHR signaling activated by environmental pollutants could have a subtle but 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 INTERESTS: This work was funded by the National Institutes of Health: ES028957, HD020676, ES029280, HD105734 and the Sosland Foundation. The authors declare no conflicts of interest.

摘要

研究问题

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?

总结答案

AHR激活导致基因表达改变,但并不妨碍滋养层细胞维持干细胞状态或分化为重要细胞类型的能力,如绒毛外滋养层细胞(EVT)或合体滋养层细胞(ST)。它还促进了2-甲氧基雌二醇(2ME)的产生,这是一种可能影响胎盘发育的化合物。

已知信息

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。

参与者/材料、环境、方法:使用人滋养层干细胞(TS)作为模型系统。研究人员检测了在干细胞状态下以及诱导分化为EVT或ST的TS细胞中,暴露于2,3,7,8-四氯二苯并对二恶英(TCDD)后的影响。该研究评估了基因表达的变化,尤其关注[具体基因]以及2ME的产生。

主要结果及机遇的作用

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[具体基因]的表达。虽然AHR激活并未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,这可能会影响胎盘功能。这些效应依赖于AHR信号通路。

局限性、谨慎的原因:本研究是在体外进行的,可能无法完全复制人体情况。需要进一步研究以确认这些发现是否适用于人类实际的胎盘发育。

研究结果的更广泛意义

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微妙但显著的影响。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以及索斯兰基金会。作者声明无利益冲突。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8dd/11867418/d534a2ef2d71/nihpp-2024.08.27.609205v2-f0001.jpg

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