单细胞拓扑简单分析揭示高阶细胞复杂性

Baihan Lin
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引用次数: 2

摘要

细胞-细胞共存及其在发育过程中形成集团的动态之间缺乏传统的联系,这阻碍了我们对细胞群体如何增殖、分化和竞争的理解,即细胞生态学。随着单细胞rna测序(RNA-seq)的最新进展,我们可以通过构建表征细胞特异性转录程序基因表达谱相似性的网络图,并利用代数拓扑的汇总统计系统地分析这些图,来潜在地描述这种联系。我们提出单细胞拓扑简单分析(scTSA)。将这种方法应用于不同发育阶段具有不同结果的细胞局部网络的单细胞基因表达谱,揭示了以前未见过的细胞生态学拓扑结构。这些网络包含了大量的单细胞群,这些单细胞群被捆绑在洞穴中,引导着更复杂的居住形式的出现。与零模型相比,我们用这些网络的拓扑简单架构来可视化这些生态模式。以斑马鱼胚胎发生的单细胞RNA-seq数据为基准,跨越38,731个细胞,25种细胞类型和12个时间步骤,我们的方法强调原肠胚形成是最关键的阶段,与发育生物学的共识一致。作为一个非线性、模型无关和无监督的框架,我们的方法也可以应用于追踪多尺度细胞谱系、识别关键阶段或创建伪时间序列。有关这项工作的扩展版本和对我们方法的系统评估,请参阅[1]了解更多细节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single-Cell Topological Simplicial Analysis Reveals Higher-Order Cellular Complexity
The absence of a conventional association between the cell-cell cohabitation and its emergent dynamics into cliques during development has hindered our understanding of how cell populations proliferate, differentiate, and compete, i.e. the cell ecology. With the recent advancement of the single-cell RNA-sequencing (RNA-seq), we can potentially describe such a link by constructing network graphs that characterize the similarity of the gene expression profiles of the cell-specific transcriptional programs, and analyzing these graphs systematically using the summary statistics informed by the algebraic topology. We propose the single-cell topological simplicial analysis (scTSA). Applying this approach to the single-cell gene expression profiles from local networks of cells in different developmental stages with different outcomes reveals a previously unseen topology of cellular ecology. These networks contain an abundance of cliques of single-cell profiles bound into cavities that guide the emergence of more complicated habitation forms. We visualize these ecological patterns with topological simplicial architectures of these networks, compared with the null models. Benchmarked on the single-cell RNA-seq data of zebrafish embryogenesis spanning 38,731 cells, 25 cell types and 12 time steps, our approach highlights the gastrulation as the most critical stage, consistent with consensus in developmental biology. As a nonlinear, model-independent, and unsupervised framework, our approach can also be applied to tracing multi-scale cell lineage, identifying critical stages, or creating pseudo-time series.11For an extended version of this work and a systematic evaluation of our approach, please refer to [1] for more details.
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