Revealing cell–cell communication pathways with their spatially coupled gene programs

Author:

Zhu Junchao1,Dai Hao1,Chen Luonan123

Affiliation:

1. Key Laboratory of Systems Biology, Shanghai Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences , Cell building, No. 320 Yueyang Road, Xuhui District, Shanghai 200031 , China

2. Key Laboratory of Systems Health Science of Zhejiang Province , School of Life Science, Hangzhou Institute for Advanced Study, , No. 1, Xiangshan Zhinong, Xihu District, Hangzhou 310024 , China

3. University of Chinese Academy of Sciences, Chinese Academy of Sciences , School of Life Science, Hangzhou Institute for Advanced Study, , No. 1, Xiangshan Zhinong, Xihu District, Hangzhou 310024 , China

Abstract

Abstract Inference of cell–cell communication (CCC) provides valuable information in understanding the mechanisms of many important life processes. With the rise of spatial transcriptomics in recent years, many methods have emerged to predict CCCs using spatial information of cells. However, most existing methods only describe CCCs based on ligand–receptor interactions, but lack the exploration of their upstream/downstream pathways. In this paper, we proposed a new method to infer CCCs, called Intercellular Gene Association Network (IGAN). Specifically, it is for the first time that we can estimate the gene associations/network between two specific single spatially adjacent cells. By using the IGAN method, we can not only infer CCCs in an accurate manner, but also explore the upstream/downstream pathways of ligands/receptors from the network perspective, which are actually exhibited as a new panoramic cell-interaction-pathway graph, and thus provide extensive information for the regulatory mechanisms behind CCCs. In addition, IGAN can measure the CCC activity at single cell/spot resolution, and help to discover the CCC spatial heterogeneity. Interestingly, we found that CCC patterns from IGAN are highly consistent with the spatial microenvironment patterns for each cell type, which further indicated the accuracy of our method. Analyses on several public datasets validated the advantages of IGAN.

Funder

Strategic Priority Research Program of the Chinese Academy of Sciences

National Key Research and Development Program of China

Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

JST Moonshot Research and Development Program

Publisher

Oxford University Press (OUP)

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