Mitchell Jacob T, Stapleton Orian, Krishnan Kavita, Nagaraj Sushma, Lvovs Dmitrijs, Cherry Christopher, Poissonnier Amanda, Horton Wes, Adey Andrew, Rao Varun, Huff Amanda, Zimmerman Jacquelyn W, Kagohara Luciane T, Zaidi Neeha, Coussens Lisa M, Jaffee Elizabeth M, Elisseeff Jeniffer H, Fertig Elana J
Department of Oncology, Sydney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, Maryland, USA.
Johns Hopkins Convergence Institute, Johns Hopkins University, Baltimore, Maryland, USA.
bioRxiv. 2025 May 3:2025.05.02.651747. doi: 10.1101/2025.05.02.651747.
Algorithms for ligand-receptor network inference have emerged as commonly used tools to estimate cell-cell communication from reference single-cell data. Many studies employ these algorithms to compare signaling between conditions and lack methods to statistically identify signals that are significantly different. We previously developed the cell communication inference algorithm Domino, which considers ligand and receptor gene expression in association with downstream transcription factor activity scoring. We developed the dominoSignal software to innovate upon Domino and extend its functionality to test statistically differential cellular signaling. This new functionality includes compilation of active signals as linkages from multiple subjects in a single-cell data set and testing condition-dependent signaling linkage. The software is applicable for analysis of single-cell data sets with multiple subjects as biological replicates as well as with bootstrapped replicates from data sets with few or pooled subjects. We use simulation studies to benchmark the number of subjects in compared groups and cells within an annotated cell type sufficient to accurately identify differential linkages. We demonstrate the application of the Differential Cell Signaling Test (DCST) in the dominoSignal software to investigate consequences of cancer cell phenotypes and immunotherapy on cell-cell communication in tumor microenvironments. These applications in cancer studies demonstrate the ability of differential cell signaling analysis to infer changes to cell communication networks from therapeutic or experimental perturbations, which is broadly applicable across biological systems.
用于配体-受体网络推断的算法已成为从参考单细胞数据估计细胞间通讯的常用工具。许多研究使用这些算法来比较不同条件下的信号传导,但缺乏统计识别显著差异信号的方法。我们之前开发了细胞通讯推断算法Domino,该算法将配体和受体基因表达与下游转录因子活性评分相结合。我们开发了dominoSignal软件,对Domino进行创新并扩展其功能,以测试统计学上的差异细胞信号传导。这项新功能包括将活跃信号编译为来自单细胞数据集中多个样本的联系,并测试条件依赖性信号联系。该软件适用于分析具有多个作为生物学重复样本的单细胞数据集,以及来自少量或合并样本数据集的自展重复样本。我们使用模拟研究来确定比较组中的样本数量以及注释细胞类型内足以准确识别差异联系的细胞数量。我们展示了dominoSignal软件中的差异细胞信号测试(DCST)在研究癌细胞表型和免疫疗法对肿瘤微环境中细胞间通讯影响方面的应用。这些在癌症研究中的应用证明了差异细胞信号分析能够从治疗或实验扰动中推断细胞通讯网络的变化能力,并广泛适用于生物系统。