Olson Audrey, Zhang Fuquan, Cao Hongbao, Baranova Ancha, Slavin Margaret
Department of Nutrition and Food Studies, College of Health and Human Services, George Mason University, Fairfax, VA, United States.
School of Systems Biology, College of Science, George Mason University, Manassas, VA, United States.
Front Neurosci. 2021 Apr 20;15:648410. doi: 10.3389/fnins.2021.648410. eCollection 2021.
Food is the primary human source of choline, an essential precursor to the neurotransmitter acetylcholine, which has a central role in signaling pathways that govern sensorimotor functions. Most Americans do not consume their recommended amount of dietary choline, and populations with neurodevelopmental conditions like autism spectrum disorder (ASD) may be particularly vulnerable to consequences of choline deficiency. This study aimed to identify a relationship between ASD and cholinergic signaling through gene set enrichment analysis and interrogation of existing database evidence to produce a systems biology model. In gene set enrichment analysis, two gene ontologies were identified as overlapping for autism-related and for cholinergic pathways-related functions, both involving ion transport regulation. Subsequent modeling of ion transport intensive cholinergic signaling pathways highlighted the importance of two genes with autism-associated variants: , which codes for the gamma aminobutyric acid receptor (GABA ), and , which codes for calcium-activated, potassium ion transporting SK2 channels responsible for membrane repolarization after cholinergic binding/signal transmission events. Cholinergic signal transmission pathways related to these proteins were examined in the Pathway Studio environment. The ion transport ontological associations indicated feasibility of a dietary choline support as a low-risk therapeutic intervention capable of modulating cholinergic sensory signaling in autism. Further research at the intersection of dietary status and sensory function in autism is warranted.
食物是人体胆碱的主要来源,胆碱是神经递质乙酰胆碱的必需前体,在控制感觉运动功能的信号通路中起核心作用。大多数美国人摄入的膳食胆碱未达到推荐量,而患有自闭症谱系障碍(ASD)等神经发育疾病的人群可能特别容易受到胆碱缺乏后果的影响。本研究旨在通过基因集富集分析和对现有数据库证据的探究,确定ASD与胆碱能信号传导之间的关系,以建立一个系统生物学模型。在基因集富集分析中,发现两个基因本体在自闭症相关功能和胆碱能途径相关功能中重叠,均涉及离子转运调节。随后对离子转运密集型胆碱能信号通路进行建模,突出了两个具有自闭症相关变体的基因的重要性:编码γ-氨基丁酸受体(GABA)的基因,以及编码钙激活钾离子转运SK2通道的基因,该通道负责胆碱能结合/信号传递事件后膜的复极化。在Pathway Studio环境中研究了与这些蛋白质相关的胆碱能信号传导途径。离子转运本体关联表明,膳食胆碱支持作为一种能够调节自闭症中胆碱能感觉信号的低风险治疗干预措施具有可行性。有必要在自闭症的饮食状况和感觉功能交叉领域进行进一步研究。