# CellGAT: A GAT-Based Method for Constructing a Cell Communication Network Integrating Multiomics Information

**Authors:** Tianjiao Zhang, Zhenao Wu, Liangyu Li, Jixiang Ren, Ziheng Zhang, Jingyu Zhang, Guohua Wang

PMC · DOI: 10.3390/biom15030342 · Biomolecules · 2025-02-27

## TL;DR

CellGAT is a new method that uses multiple data types to accurately predict how cells communicate with each other.

## Contribution

CellGAT integrates PPIs, gene expression, and pathway data to improve cell communication predictions.

## Key findings

- CellGAT outperforms existing methods in predicting cell-cell communication.
- The method accurately identifies communication impacts on pathways and drug responses.
- CellGAT includes a built-in clustering algorithm for cell type identification.

## Abstract

The growth, development, and differentiation of multicellular organisms are primarily driven by intercellular communication, which coordinates the activities of diverse cell types. This cell-to-cell signaling is typically mediated by various types of protein–protein interactions, including ligand–receptor; receptor–receptor, and extracellular matrix–receptor interactions. Currently, computational methods for inferring ligand–receptor communication primarily depend on gene expression data of ligand–receptor pairs and spatial information of cells. Some approaches integrate protein complexes; transcription factors; or pathway information to construct cell communication networks. However, few methods consider the critical role of protein–protein interactions (PPIs) in intercellular communication networks, especially when predicting communication between different cell types in the absence of cell type information. These methods often rely on ligand–receptor pairs that lack PPI evidence, potentially compromising the accuracy of their predictions. To address this issue, we propose CellGAT, a framework that infers intercellular communication by integrating gene expression data of ligand–receptor pairs, PPI information, protein complex data, and experimentally validated pathway information. CellGAT not only builds a priori models but also uses node embedding algorithms and graph attention networks to build cell communication networks based on scRNA-seq (single-cell RNA sequencing) datasets and includes a built-in cell clustering algorithm. Through comparisons with various methods, CellGAT accurately predicts cell–cell communication (CCC) and analyzes its impact on downstream pathways; neighboring cells; and drug interventions.

## Full-text entities

- **Genes:** ITGB1 (integrin subunit beta 1) [NCBI Gene 3688] {aka CD29, FNRB, GPIIA, MDF2, MSK12, VLA-BETA}, SH2B2 (SH2B adaptor protein 2) [NCBI Gene 10603] {aka APS}, TTC19 (tetratricopeptide repeat domain 19) [NCBI Gene 54902] {aka 2010204O13Rik, MC3DN2}, Pld (Phospholipase D) [NCBI Gene 35554] {aka CG12110, Dmel\CG12110, MitoPLD, PC-Pld, dPLD, dPld}, CXCL12 (C-X-C motif chemokine ligand 12) [NCBI Gene 6387] {aka IRH, PBSF, SCYB12, SDF1, TLSF, TPAR1}, GRB2 (growth factor receptor bound protein 2) [NCBI Gene 2885] {aka ASH, EGFRBP-GRB2, Grb3-3, MST084, MSTP084, NCKAP2}, rl (rolled) [NCBI Gene 3354888] {aka 12559, BcDNA:RE08694, CG12559, CG18732, CT34260, CT39192}, CXCR4 (C-X-C motif chemokine receptor 4) [NCBI Gene 7852] {aka CD184, D2S201E, FB22, HM89, HSY3RR, LCR1}, N (Notch) [NCBI Gene 31293] {aka 1.1, 16-178, 16-55, Ax, CG3936, CT13012}, RELN (reelin) [NCBI Gene 5649] {aka ETL7, LIS2, PRO1598, RL}, RPS11 (ribosomal protein S11) [NCBI Gene 6205] {aka S11, uS17}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, SHC1 (SHC adaptor protein 1) [NCBI Gene 6464] {aka SHC, SHCA}
- **Diseases:** myocardial infarction (MESH:D009203), tumorigenic (MESH:D002471), metastasis (MESH:D009362), glioblastoma (MESH:D005909), CCC (MESH:D002292), heart (MESH:D006331), ischemic (MESH:D002545), cancer (MESH:D009369), lung cancer (MESH:D008175), neural damage (MESH:D015441), fibrosis (MESH:D005355), injury to (MESH:D014947), inflammatory (MESH:D007249), Burkitt's lymphoma (MESH:D002051), lung adenocarcinoma (MESH:D000077192)
- **Chemicals:** phosphotyrosine (MESH:D019000), LR (-), osimertinib (MESH:C000596361), tyrosine (MESH:D014443)
- **Species:** Homo sapiens (human, species) [taxon 9606], Drosophila melanogaster (fruit fly, species) [taxon 7227], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** Thr790Met
- **Cell lines:** PC9 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_B260), PC9 lung adenocarcinoma — Canis lupus familiaris (Dog), Canine lung adenocarcinoma, Cancer cell line (CVCL_J360), S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11940051/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC11940051/full.md

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Source: https://tomesphere.com/paper/PMC11940051