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Integrating single-cell transcriptomic data across different conditions, technologies, and species.整合不同条件、技术和物种的单细胞转录组数据。
Nat Biotechnol. 2018 Jun;36(5):411-420. doi: 10.1038/nbt.4096. Epub 2018 Apr 2.
2
Notch signaling pathway networks in cancer metastasis: a new target for cancer therapy.癌症转移中的 Notch 信号通路网络:癌症治疗的新靶点。
Med Oncol. 2017 Sep 16;34(10):180. doi: 10.1007/s12032-017-1039-6.
3
Notch: an interactive player in neurogenesis and disease.Notch:神经发生和疾病中的交互参与者。
Cell Tissue Res. 2018 Jan;371(1):73-89. doi: 10.1007/s00441-017-2641-9. Epub 2017 Jun 15.
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Wnt/β-Catenin Signaling, Disease, and Emerging Therapeutic Modalities.Wnt/β-连环蛋白信号通路、疾病与新兴治疗模式。
Cell. 2017 Jun 1;169(6):985-999. doi: 10.1016/j.cell.2017.05.016.
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The Wnt signaling pathway in cancer.癌症中的Wnt信号通路。
Crit Rev Oncol Hematol. 2016 Mar;99:141-9. doi: 10.1016/j.critrevonc.2015.12.005. Epub 2015 Dec 24.
6
Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets.利用纳升液滴对单个细胞进行高度并行的全基因组表达谱分析。
Cell. 2015 May 21;161(5):1202-1214. doi: 10.1016/j.cell.2015.05.002.
7
Specific functions of the Wnt signaling system in gene regulatory networks throughout the early sea urchin embryo.Wnt信号系统在整个海胆早期胚胎基因调控网络中的特定功能。
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Short-range Wnt5 signaling initiates specification of sea urchin posterior ectoderm.短距离 Wnt5 信号启动海胆后外胚层的特化。
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9
Notch and Nodal control forkhead factor expression in the specification of multipotent progenitors in sea urchin.Notch 和 Nodal 控制叉头框因子表达在海胆多能祖细胞的特化中。
Development. 2013 Apr;140(8):1796-806. doi: 10.1242/dev.091157.
10
Integration of canonical and noncanonical Wnt signaling pathways patterns the neuroectoderm along the anterior-posterior axis of sea urchin embryos.经典和非经典 Wnt 信号通路的整合沿着海胆胚胎的前后轴模式化神经外胚层。
PLoS Biol. 2013;11(1):e1001467. doi: 10.1371/journal.pbio.1001467. Epub 2013 Jan 15.

单细胞 RNA 测序显示海胆胚胎中的 Delta/Notch 通路具有明显的细胞类型特异性。

Single cell RNA-seq in the sea urchin embryo show marked cell-type specificity in the Delta/Notch pathway.

机构信息

Department of Molecular and Cell Biology and Biochemistry, Brown University, Providence, Rhode Island.

出版信息

Mol Reprod Dev. 2019 Aug;86(8):931-934. doi: 10.1002/mrd.23181. Epub 2019 Jun 14.

DOI:10.1002/mrd.23181
PMID:31199038
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6690749/
Abstract

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.

摘要

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。