OrgaCCC: Orthogonal graph autoencoders for constructing cell-cell communication networks on spatial transcriptomics data.

IF 3.6 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
PLoS Computational Biology Pub Date : 2025-06-27 eCollection Date: 2025-06-01 DOI:10.1371/journal.pcbi.1013212
Xixuan Feng, Shuqin Zhang, Limin Li
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引用次数: 0

Abstract

Cell-cell communication (CCC) is a fundamental biological process essential for maintaining the functionality of multicellular organisms. It allows cells to coordinate their activities, sustain tissue homeostasis, and adapt to environmental changes. However, understanding the mechanisms underlying intercellular communication remains challenging. The rapid advancements in spatial transcriptomics (ST) have enabled the analysis of CCC within its spatial context. Despite the development of several computational methods for inferring CCCs from ST data, most rely on literature-curated gene or protein interaction lists, which are often inadequate due to the restricted gene coverage. In this work, we propose OrgaCCC, an orthogonal graph autoencoders approach for cell-cell communication inference based on deep generative models. OrgaCCC leverages the information of gene expression profiles, spatial locations and ligand-receptor relationships. It captures both cell/spot and gene features using two orthogonally coupled variational graph autoencoders across cell/spot and gene dimensions and combines them by maximizing the similarity between their reconstructed cell/spot features. Numerical experiments on five ST datasets demonstrate the superiority of OrgaCCC compared with state-of-the-art methods in CCC inference at the cell-type level, cell/spot level, and ligand-receptor level, in terms of inference accuracy and reliability.

基于空间转录组学数据构建细胞-细胞通信网络的正交图自编码器。
细胞间通讯(CCC)是维持多细胞生物功能的基本生物学过程。它允许细胞协调它们的活动,维持组织稳态,并适应环境变化。然而,了解细胞间通讯的机制仍然具有挑战性。空间转录组学(ST)的快速发展使得在其空间背景下分析CCC成为可能。尽管开发了几种从ST数据推断CCCs的计算方法,但大多数依赖于文献整理的基因或蛋白质相互作用列表,由于基因覆盖范围有限,这些列表往往不充分。在这项工作中,我们提出了OrgaCCC,一种基于深度生成模型的细胞-细胞通信推理的正交图自编码器方法。OrgaCCC利用基因表达谱、空间位置和配体-受体关系的信息。它使用两个跨细胞/斑点和基因维度的正交耦合变分图自编码器捕获细胞/斑点和基因特征,并通过最大化其重构细胞/斑点特征之间的相似性来组合它们。在5个ST数据集上的数值实验表明,在细胞类型水平、细胞/斑点水平和配体受体水平上,OrgaCCC在推断精度和可靠性方面优于现有的CCC推断方法。
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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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