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人类胚胎脑发育的胚胎干细胞模型中谱系分支的单细胞路线图。

A Single-Cell Roadmap of Lineage Bifurcation in Human ESC Models of Embryonic Brain Development.

作者信息

Yao Zizhen, Mich John K, Ku Sherman, Menon Vilas, Krostag Anne-Rachel, Martinez Refugio A, Furchtgott Leon, Mulholland Heather, Bort Susan, Fuqua Margaret A, Gregor Ben W, Hodge Rebecca D, Jayabalu Anu, May Ryan C, Melton Samuel, Nelson Angelique M, Ngo N Kiet, Shapovalova Nadiya V, Shehata Soraya I, Smith Michael W, Tait Leah J, Thompson Carol L, Thomsen Elliot R, Ye Chaoyang, Glass Ian A, Kaykas Ajamete, Yao Shuyuan, Phillips John W, Grimley Joshua S, Levi Boaz P, Wang Yanling, Ramanathan Sharad

机构信息

Allen Institute for Brain Science, Seattle, WA 98109, USA.

Molecular and Cellular Biology Department, Harvard University, Cambridge, MA 02138, USA.

出版信息

Cell Stem Cell. 2017 Jan 5;20(1):120-134. doi: 10.1016/j.stem.2016.09.011. Epub 2016 Oct 27.

Abstract

During human brain development, multiple signaling pathways generate diverse cell types with varied regional identities. Here, we integrate single-cell RNA sequencing and clonal analyses to reveal lineage trees and molecular signals underlying early forebrain and mid/hindbrain cell differentiation from human embryonic stem cells (hESCs). Clustering single-cell transcriptomic data identified 41 distinct populations of progenitor, neuronal, and non-neural cells across our differentiation time course. Comparisons with primary mouse and human gene expression data demonstrated rostral and caudal progenitor and neuronal identities from early brain development. Bayesian analyses inferred a unified cell-type lineage tree that bifurcates between cortical and mid/hindbrain cell types. Two methods of clonal analyses confirmed these findings and further revealed the importance of Wnt/β-catenin signaling in controlling this lineage decision. Together, these findings provide a rich transcriptome-based lineage map for studying human brain development and modeling developmental disorders.

摘要

在人类大脑发育过程中,多种信号通路产生具有不同区域特征的多种细胞类型。在这里,我们整合单细胞RNA测序和克隆分析,以揭示人类胚胎干细胞(hESCs)早期前脑和中/后脑细胞分化的谱系树和分子信号。对单细胞转录组数据进行聚类,在我们的分化时间进程中识别出41个不同的祖细胞、神经元细胞和非神经细胞群体。与原代小鼠和人类基因表达数据的比较表明,早期大脑发育中存在前侧和后侧祖细胞及神经元特征。贝叶斯分析推断出一个统一的细胞类型谱系树,该谱系树在皮质和中/后脑细胞类型之间分叉。两种克隆分析方法证实了这些发现,并进一步揭示了Wnt/β-连环蛋白信号在控制这一谱系决定中的重要性。总之,这些发现为研究人类大脑发育和模拟发育障碍提供了一个丰富的基于转录组的谱系图谱。

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