Feng Jiarui, Province Michael, Li Guangfu, Payne Philip R O, Chen Yixin, Li Fuhai
Institute for Informatics (I2), Washington University School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Department of Computer Science and Engineering, Washington University School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
bioRxiv. 2024 Jan 15:2024.01.13.575534. doi: 10.1101/2024.01.13.575534.
Recently, large-scale scRNA-seq datasets have been generated to understand the complex and poorly understood signaling mechanisms within microenvironment of Alzheimer's Disease (AD), which are critical for identifying novel therapeutic targets and precision medicine. Though a set of targets have been identified, however, it remains a challenging to infer the core intra- and inter-multi-cell signaling communication networks using the scRNA-seq data, considering the complex and highly interactive background signaling network. Herein, we introduced a novel graph transformer model, PathFinder, to infer multi-cell intra- and inter-cellular signaling pathways and signaling communications among multi-cell types. Compared with existing models, the novel and unique design of PathFinder is based on the divide-and-conquer strategy, which divides the complex signaling networks into signaling paths, and then score and rank them using a novel graph transformer architecture to infer the intra- and inter-cell signaling communications. We evaluated PathFinder using scRNA-seq data of APOE4-genotype specific AD mice models and identified novel APOE4 altered intra- and inter-cell interaction networks among neurons, astrocytes, and microglia. PathFinder is a general signaling network inference model and can be applied to other omics data-driven signaling network inference.
最近,为了了解阿尔茨海默病(AD)微环境中复杂且鲜为人知的信号传导机制,已经生成了大规模的单细胞RNA测序(scRNA-seq)数据集,这对于识别新的治疗靶点和精准医学至关重要。尽管已经确定了一组靶点,然而,考虑到复杂且高度交互的背景信号网络,使用scRNA-seq数据推断核心的多细胞内和细胞间信号通信网络仍然具有挑战性。在此,我们引入了一种新型的图Transformer模型PathFinder,以推断多细胞内和细胞间的信号通路以及多细胞类型之间的信号通信。与现有模型相比,PathFinder新颖独特的设计基于分治策略,即将复杂的信号网络划分为信号路径,然后使用新型的图Transformer架构对其进行评分和排序,以推断细胞内和细胞间的信号通信。我们使用APOE4基因型特异性AD小鼠模型的scRNA-seq数据对PathFinder进行了评估,并确定了APOE4在神经元、星形胶质细胞和小胶质细胞之间改变的新型细胞内和细胞间相互作用网络。PathFinder是一种通用的信号网络推断模型,可应用于其他组学数据驱动的信号网络推断。