Liu Wenlong, Li Liming, Xia Xiaochun, Zhou Xulan, Du Yukai, Yin Zhaoqing, Wang Juan
Department of Child Development and Behavior, School of Medicine, Women and Children's Hospital, Xiamen University, Xiamen, China.
Department of Public Health and Medical Technology, Xiamen Medical College, Xiamen, China.
Front Psychiatry. 2022 May 9;13:780747. doi: 10.3389/fpsyt.2022.780747. eCollection 2022.
Autism spectrum disorder (ASD) comprises a group of neurodevelopmental disorders whose etiology and pathogenesis are not fully understood. To gain insight into the molecular basis of ASD, we performed comparative integrated proteomic and metabolomic analyses of urine samples from children diagnosed with ASD and healthy children. All 160 samples underwent proteomics analysis and 60 were analyzed by liquid chromatography-mass spectrometry to obtain metabolite profiles. We identified 77 differentially expressed proteins (DEPs; 21 downregulated and 56 upregulated) and 277 differentially expressed metabolites; 31 of the DEPs including glutathione, leukocyte antigens, glycoproteins, neural adhesion factors, and immunoglobulins, have been implicated in neuroinflammation. The proteomic analysis also revealed 8 signaling pathways that were significantly dysregulated in ASD patients; 3 of these (transendothelial leukocyte migration, antigen processing and presentation, and graft vs. host disease) were associated with the neuroimmune response. The metabolism of tryptophan, which is also related to the neuroimmune response, has been found to play a potential role in ASD. Integrated proteome and metabolome analysis showed that 6 signaling pathways were significantly enriched in ASD patients, 3 of which were correlated with impaired neuroinflammation (glutathione metabolism, metabolism of xenobiotics by cytochrome P450 and transendothelial migration of leukocyte). We also found a correlation between prostaglandin (PG) E2 levels and the inflammatory response in ASD. These results underscore the prominent role of the neuroimmune response in ASD and provide potential biomarkers that can be used for diagnosis or as targets for early intervention.
自闭症谱系障碍(ASD)是一组神经发育障碍,其病因和发病机制尚未完全明确。为深入了解ASD的分子基础,我们对自闭症患儿和健康儿童的尿液样本进行了比较性综合蛋白质组学和代谢组学分析。所有160份样本均进行了蛋白质组学分析,其中60份通过液相色谱 - 质谱联用技术进行分析以获得代谢物谱。我们鉴定出77种差异表达蛋白(DEP;21种下调和56种上调)和277种差异表达代谢物;其中31种DEP,包括谷胱甘肽、白细胞抗原、糖蛋白、神经粘附因子和免疫球蛋白,与神经炎症有关。蛋白质组学分析还揭示了8条在ASD患者中显著失调的信号通路;其中3条(跨内皮白细胞迁移、抗原加工和呈递以及移植物抗宿主病)与神经免疫反应相关。色氨酸代谢也与神经免疫反应有关,已发现其在ASD中发挥潜在作用。综合蛋白质组和代谢组分析表明,6条信号通路在ASD患者中显著富集,其中3条与神经炎症受损相关(谷胱甘肽代谢、细胞色素P450对外源化合物的代谢以及白细胞的跨内皮迁移)。我们还发现前列腺素(PG)E2水平与ASD中的炎症反应之间存在相关性。这些结果强调了神经免疫反应在ASD中的突出作用,并提供了可用于诊断或作为早期干预靶点的潜在生物标志物。