Jia Gong-Xue, Ma Wen-Ji, Wu Zhao-Bo, Li Shuang, Zhang Xiao-Qian, He Zhen, Wu Shi-Xin, Tao Hai-Ping, Fang Yi, Song Yong-Wu, Xu Shang-Rong, Wang Xiao-Qun, Yang Qi-En
Key Laboratory of Adaptation and Evolution of Plateau Biota, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining 810001, China; University of Chinese Academy of Sciences, Beijing 100049, China; Qinghai Key Laboratory of Animal Ecological Genomics, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining 810001, China.
State Key Laboratory of Brain and Cognitive Science, CAS Center for Excellence in Brain Science and Intelligence Technology, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China; Center for Single-Cell Omics, School of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Cell Rep. 2023 Aug 29;42(8):112860. doi: 10.1016/j.celrep.2023.112860. Epub 2023 Jul 25.
Bidirectional communication between the developing conceptus and endometrium is essential for pregnancy recognition and establishment in ruminants. We dissect the transcriptomic dynamics of sheep conceptus and corresponding endometrium at pre- and peri-implantation stages using single-cell RNA sequencing. Spherical blastocysts contain five cell types, with 68.62% trophectoderm cells. Strikingly, elongated conceptuses differentiate into 17 cell types, indicating dramatic cell fate specifications. Cell-type-specific gene expression delineates the features of distinctive trophectoderm lineages and indicates that the transition from polar trophectoderm to trophoblast increases interferon-tau expression and likely drives elongation initiation. We identify 13 endometrium-derived cell types and elucidate their molecular responses to conceptus development. Integrated analyses uncover multiple paired transcripts mediating the dialogues between extraembryonic membrane and endometrium, including IGF2-IGF1R, FGF19-FGFR1, NPY-NPY1R, PROS1-AXL, and ADGRE5-CD55. These data provide insight into the molecular regulation of conceptus elongation and represent a valuable resource for functional investigations of pre- and peri-implantation ruminant development.
在反刍动物中,发育中的孕体与子宫内膜之间的双向通讯对于妊娠识别和建立至关重要。我们使用单细胞RNA测序剖析了绵羊孕体和相应子宫内膜在植入前和植入周围阶段的转录组动态。球形囊胚包含五种细胞类型,其中滋养外胚层细胞占68.62%。令人惊讶的是,伸长的孕体分化为17种细胞类型,表明细胞命运发生了显著的特化。细胞类型特异性基因表达描绘了独特的滋养外胚层谱系的特征,并表明从极滋养外胚层向滋养层的转变会增加干扰素-τ的表达,并可能驱动伸长的起始。我们鉴定出13种子宫内膜来源的细胞类型,并阐明了它们对孕体发育的分子反应。综合分析揭示了多个介导胚外膜与子宫内膜之间对话的配对转录本,包括IGF2-IGF1R、FGF19-FGFR1、NPY-NPY1R、PROS1-AXL和ADGRE5-CD55。这些数据为孕体伸长的分子调控提供了见解,并代表了反刍动物植入前和植入周围发育功能研究的宝贵资源。