Xia Hong, Ji Boya, Qiao Debin, Peng Shaoliang
College of Computer Science and Electronic Engineering, Hunan University, Changsha 410082, China.
School of Computer and Artificial Intelligence, ZhengZhou University, Zhengzhou 450001, China.
Brief Bioinform. 2024 Nov 22;26(1). doi: 10.1093/bib/bbae716.
The role of cell-cell communications (CCCs) is increasingly recognized as being important to differentiation, invasion, metastasis, and drug resistance in tumoral tissues. Developing CCC inference methods using traditional experimental methods are time-consuming, labor-intensive, cannot handle large amounts of data. To facilitate inference of CCCs, we proposed a computational framework, called CellMsg, which involves two primary steps: identifying ligand-receptor interactions (LRIs) and measuring the strength of LRIs-mediated CCCs. Specifically, CellMsg first identifies high-confident LRIs based on multimodal features of ligands and receptors and graph convolutional networks. Then, CellMsg measures the strength of intercellular communication by combining the identified LRIs and single-cell RNA-seq data using a three-point estimation method. Performance evaluation on four benchmark LRI datasets by five-fold cross validation demonstrated that CellMsg accurately captured the relationships between ligands and receptors, resulting in the identification of high-confident LRIs. Compared with other methods of identifying LRIs, CellMsg has better prediction performance and robustness. Furthermore, the LRIs identified by CellMsg were successfully validated through molecular docking. Finally, we examined the overlap of LRIs between CellMsg and five other classical CCC databases, as well as the intercellular crosstalk among seven cell types within a human melanoma tissue. In summary, CellMsg establishes a complete, reliable, and well-organized LRI database and an effective CCC strength evaluation method for each single-cell RNA-seq data. It provides a computational tool allowing researchers to decipher intercellular communications. CellMsg is freely available at https://github.com/pengsl-lab/CellMsg.
细胞间通讯(CCC)在肿瘤组织的分化、侵袭、转移和耐药性方面的重要作用日益受到认可。利用传统实验方法开发CCC推断方法既耗时又费力,且无法处理大量数据。为了便于推断CCC,我们提出了一个名为CellMsg的计算框架,它包括两个主要步骤:识别配体-受体相互作用(LRI)以及测量LRI介导的CCC的强度。具体而言,CellMsg首先基于配体和受体的多模态特征以及图卷积网络识别高置信度的LRI。然后,CellMsg使用三点估计方法,通过结合识别出的LRI和单细胞RNA测序数据来测量细胞间通讯的强度。通过五折交叉验证在四个基准LRI数据集上进行的性能评估表明,CellMsg准确地捕捉到了配体和受体之间的关系,从而识别出高置信度的LRI。与其他识别LRI的方法相比,CellMsg具有更好的预测性能和稳健性。此外,通过分子对接成功验证了CellMsg识别出的LRI。最后,我们研究了CellMsg与其他五个经典CCC数据库之间LRI的重叠情况,以及人类黑色素瘤组织中七种细胞类型之间的细胞间串扰。总之,CellMsg为每个单细胞RNA测序数据建立了一个完整、可靠且组织良好的LRI数据库以及一种有效的CCC强度评估方法。它提供了一个计算工具,使研究人员能够解读细胞间通讯。CellMsg可在https://github.com/pengsl-lab/CellMsg上免费获取。