Department of Molecular and Cell Biology and Biochemistry, Brown University, Providence, Rhode Island.
Mol Reprod Dev. 2019 Aug;86(8):931-934. doi: 10.1002/mrd.23181. Epub 2019 Jun 14.
Sea urchin embryos are excellent for in vivo functional studies because of their transparency and tractability in manipulation. They are also favorites for pharmacological approaches since they develop in an aquatic environment and addition of test substances is straightforward. A concern in many pharmacological tests though is the potential for pleiotropic effects that confound the conclusions drawn from the results. Precise cellular interpretations are often not feasible because the impact of the perturbant is not known. Here we use single-cell mRNA (messenger RNA) sequencing as a metric of cell types in the embryo and to determine the selectivity of two commonly used inhibitors, one each for the Wnt and the Delta-Notch pathways, on these nascent cell types. We identified 11 distinct cell types based on mRNA profiling, and that the cell lineages affected by Wnt and Delta/Notch inhibition were distinct from each other. These data support specificity and distinct effects of these signaling pathways in the embryo and illuminate how these conserved pathways selectively regulate cell lineages at a single cell level. Overall, we conclude that single cell RNA-seq analysis in this embryo is revealing of the cell types present during development, of the changes in the gene regulatory network resulting from inhibition of various signaling pathways, and of the selectivity of these pathways in influencing developmental trajectories.
海胆胚胎是进行体内功能研究的理想选择,因为它们具有透明性,并且在操作过程中易于处理。它们也是药理学方法的首选,因为它们在水生环境中发育,并且添加测试物质非常简单。然而,许多药理学测试的一个关注点是多效性效应的潜在风险,这会混淆从结果中得出的结论。由于扰动剂的影响未知,因此通常无法进行精确的细胞解释。在这里,我们使用单细胞 mRNA(信使 RNA)测序作为胚胎中细胞类型的衡量标准,并确定两种常用抑制剂(一种用于 Wnt 途径,另一种用于 Delta-Notch 途径)对这些新生细胞类型的选择性。我们根据 mRNA 分析鉴定了 11 种不同的细胞类型,并且 Wnt 和 Delta/Notch 抑制作用所影响的细胞谱系彼此不同。这些数据支持这些信号通路在胚胎中的特异性和独特作用,并阐明了这些保守信号通路如何在单细胞水平上选择性地调节细胞谱系。总的来说,我们得出结论,该胚胎中的单细胞 RNA-seq 分析揭示了发育过程中存在的细胞类型、各种信号通路抑制导致的基因调控网络变化,以及这些通路在影响发育轨迹方面的选择性。