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来自再生细胞模型的滋养层细胞与植入前人类胚胎的转录组比较†

Transcriptome comparisons of trophoblasts from regenerative cell models with peri-implantation human embryos†.

作者信息

Logsdon Deirdre M, Ming Hao, Ezashi Toshihiko, West Rachel C, Schoolcraft William B, Roberts R Michael, Jiang Zongliang, Yuan Ye

机构信息

Colorado Center for Reproductive Medicine, 10290 RidgeGate Circle, Lone Tree, CO 80124, USA.

Department of Animal Sciences, Genetics Institute, University of Florida, Gainesville, FL 32610, USA.

出版信息

Biol Reprod. 2024 Nov 11;111(5):1000-1016. doi: 10.1093/biolre/ioae120.

Abstract

Mechanisms controlling trophoblast (TB) proliferation and differentiation during embryo implantation are poorly understood. Human trophoblast stem cells (TSC) and BMP4/A83-01/PD173074-treated pluripotent stem cell-derived trophoblast cells (BAP) are two widely employed, contemporary models to study TB development and function, but how faithfully they mimic early TB cells has not been fully examined. We evaluated the transcriptomes of TB cells from BAP and TSC and directly compared them with those from peri-implantation human embryos during extended embryo culture (EEC) between embryonic days 8 to 12. The BAP and TSC grouped closely with TB cells from EEC within each TB sublineage following dimensional analysis and unsupervised hierarchical clustering. However, subtle differences in transcriptional programs existed within each TB sublineage. We also validated the presence of six genes in peri-implantation human embryos by immunolocalization. Our analysis reveals that both BAP and TSC models have features of peri-implantation TB s, while maintaining minor transcriptomic differences, and thus serve as valuable tools for studying implantation in lieu of human embryos.

摘要

胚胎植入过程中控制滋养层细胞(TB)增殖和分化的机制目前尚不清楚。人滋养层干细胞(TSC)以及经骨形态发生蛋白4(BMP4)/A83 - 01/PD173074处理的多能干细胞来源的滋养层细胞(BAP)是目前广泛用于研究TB发育和功能的两种当代模型,但它们对早期TB细胞的模拟程度究竟如何,尚未得到充分研究。我们评估了BAP和TSC来源的TB细胞的转录组,并将其与在胚胎发育第8至12天进行延长胚胎培养(EEC)期间的植入期人类胚胎的转录组进行了直接比较。经过维度分析和无监督层次聚类后,BAP和TSC在每个TB亚谱系中与EEC来源的TB细胞紧密聚类。然而,每个TB亚谱系内的转录程序存在细微差异。我们还通过免疫定位验证了植入期人类胚胎中六个基因的存在。我们的分析表明,BAP和TSC模型都具有植入期TB的特征,同时保持了微小的转录组差异,因此可作为替代人类胚胎研究植入过程的有价值工具。

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