小鼠胎盘的时空转录组图谱

IF 13 1区 生物学 Q1 CELL BIOLOGY
Yanting Wu, Kaizhen Su, Ying Zhang, Langchao Liang, Fei Wang, Siyue Chen, Ling Gao, Qiutong Zheng, Cheng Li, Yunfei Su, Yiting Mao, Simeng Zhu, Chaochao Chai, Qing Lan, Man Zhai, Xin Jin, Jinglan Zhang, Xun Xu, Yu Zhang, Ya Gao, Hefeng Huang
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引用次数: 0

摘要

胎盘是支撑妊娠的一个临时但不可或缺的器官,在整个妊娠过程中经历着复杂的形态和功能转变。然而,人们对胎盘的时空基因表达模式仍然知之甚少。我们利用立体测序技术构建了小鼠胎盘时空转录组图谱(MPSTA),时间跨度从胚胎第(E)天 7.5 到第 14.5 天,其中包括以前的单细胞图谱未捕获的大滋养层细胞转录组。我们定义了外胚层锥体(一种早期异质滋养层结构)的四个不同层,并阐明了E9.5之前着床后早期滋养层分化的空间轨迹。我们的时空配体-受体相互作用分析以小鼠胎盘的营养交换界面迷宫区为重点,揭示了滋养层发育和胎盘血管生成所必需的关键调节因子。我们还发现,父系表达的基因只富集在胎盘而不是蜕膜区,包括富集在内皮细胞中的一组基因,它们可能在胎盘血管生成中发挥作用。在入侵前沿,我们发现了参与妊娠维持的界面特异性转录因子调节子,如 Atf3、Jun、Junb、Stat6、Mxd1、Maff、Fos 和 Irf7。此外,我们还发现母体高脂饮食会优先影响这一界面,加剧炎症反应并破坏血管生成平衡。总之,我们的研究结果提供了一个全面的空间解析图谱,为今后探索胎盘形态发生和病理学提供了宝贵的见解和基准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A spatiotemporal transcriptomic atlas of mouse placentation.

The placenta, a temporary but essential organ for gestational support, undergoes intricate morphological and functional transformations throughout gestation. However, the spatiotemporal patterns of gene expression underlying placentation remain poorly understood. Utilizing Stereo-seq, we constructed a Mouse Placentation Spatiotemporal Transcriptomic Atlas (MPSTA) spanning from embryonic day (E) 7.5 to E14.5, which includes the transcriptomes of large trophoblast cells that were not captured in previous single-cell atlases. We defined four distinct strata of the ectoplacental cone, an early heterogeneous trophectoderm structure, and elucidated the spatial trajectory of trophoblast differentiation during early postimplantation stages before E9.5. Focusing on the labyrinth region, the interface of nutrient exchange in the mouse placenta, our spatiotemporal ligand-receptor interaction analysis unveiled pivotal modulators essential for trophoblast development and placental angiogenesis. We also found that paternally expressed genes are exclusively enriched in the placenta rather than in the decidual regions, including a cluster of genes enriched in endothelial cells that may function in placental angiogenesis. At the invasion front, we identified interface-specific transcription factor regulons, such as Atf3, Jun, Junb, Stat6, Mxd1, Maff, Fos, and Irf7, involved in gestational maintenance. Additionally, we revealed that maternal high-fat diet exposure preferentially affects this interface, exacerbating inflammatory responses and disrupting angiogenic homeostasis. Collectively, our findings furnish a comprehensive, spatially resolved atlas that offers valuable insights and benchmarks for future explorations into placental morphogenesis and pathology.

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来源期刊
Cell Discovery
Cell Discovery Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
24.20
自引率
0.60%
发文量
120
审稿时长
20 weeks
期刊介绍: Cell Discovery is a cutting-edge, open access journal published by Springer Nature in collaboration with the Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences (CAS). Our aim is to provide a dynamic and accessible platform for scientists to showcase their exceptional original research. Cell Discovery covers a wide range of topics within the fields of molecular and cell biology. We eagerly publish results of great significance and that are of broad interest to the scientific community. With an international authorship and a focus on basic life sciences, our journal is a valued member of Springer Nature's prestigious Molecular Cell Biology journals. In summary, Cell Discovery offers a fresh approach to scholarly publishing, enabling scientists from around the world to share their exceptional findings in molecular and cell biology.
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