Hosie S, Abo-Shaban T, Lee C Y Q, Matta S M, Shindler A, Gore R, Sharna S S, Herath M, Crack P J, Franks A E, Hill-Yardin E L
School of Health & Biomedical Sciences, STEM College, RMIT University, Bundoora, VIC, Australia.
Department of Physiology, Anatomy and Microbiology, La Trobe University, Bundoora, VIC, Australia.
Adv Exp Med Biol. 2022;1383:141-156. doi: 10.1007/978-3-031-05843-1_14.
Autism spectrum disorder (ASD; autism) is a prevalent neurodevelopmental disorder associated with changes in gut-brain axis communication. Gastrointestinal (GI) symptoms are experienced by a large proportion of individuals diagnosed with autism. Several mutations associated with autism modify cellular communication via neuronal synapses. It has been suggested that modifications to the enteric nervous system, an intrinsic nervous system of the GI tract, could contribute to GI dysfunction. Changes in gut motility, permeability, and the mucosal barrier as well as shifts in the large population of microbes inhabiting the GI tract could contribute to GI symptoms. Preclinical research has demonstrated that mice expressing the well-studied R451C missense mutation in Nlgn3 gene, which encodes cell adhesion protein neuroligin-3 at neuronal synapses, exhibit GI dysfunction. Specifically, NL3 mice show altered colonic motility and faster small intestinal transit. As well as dysmotility, macrophages located within the gut-associated lymphoid tissue of the NL3 mouse caecum show altered morphology, suggesting that neuro-inflammation pathways are modified in this model. Interestingly, NL3 mice maintained in a shared environment demonstrate fecal microbial dysbiosis indicating a role for the nervous system in regulating gut microbial populations. To better understand host-microbe interactions, further clarification and comparison of clinical and animal model profiles of dysbiosis should be obtained, which in turn will provide better insights into the efforts taken to design personalized microbial therapies. In addition to changes in neurophysiological measures, the mucosal component of the GI barrier may contribute to GI dysfunction more broadly in individuals diagnosed with a wide range of neurological disorders. As the study of GI dysfunction advances to encompass multiple components of the gut-brain-microbiota axis, findings will help understand future directions such as microbiome engineering and optimisation of the mucosal barrier for health.
自闭症谱系障碍(ASD;自闭症)是一种常见的神经发育障碍,与肠-脑轴通讯的变化有关。很大一部分被诊断为自闭症的个体都有胃肠道(GI)症状。一些与自闭症相关的突变通过神经元突触改变细胞通讯。有人提出,对胃肠道的内在神经系统——肠神经系统的改变可能导致胃肠功能障碍。肠道蠕动、通透性和黏膜屏障的变化,以及栖息在胃肠道中的大量微生物的变化,都可能导致胃肠道症状。临床前研究表明,在Nlgn3基因中表达经过充分研究的R451C错义突变的小鼠,该基因在神经元突触处编码细胞粘附蛋白神经连接蛋白-3,表现出胃肠功能障碍。具体而言,NL3小鼠的结肠蠕动改变,小肠转运加快。除了运动障碍外,NL3小鼠盲肠的肠道相关淋巴组织中的巨噬细胞形态也发生了改变,这表明该模型中的神经炎症途径发生了改变。有趣的是,饲养在共享环境中的NL3小鼠表现出粪便微生物群落失调,表明神经系统在调节肠道微生物群落方面发挥了作用。为了更好地理解宿主-微生物相互作用,应该进一步澄清和比较临床和动物模型中失调的情况,这反过来将为设计个性化微生物疗法的努力提供更好的见解。除了神经生理学指标的变化外,胃肠道屏障的黏膜成分可能在更广泛的被诊断患有多种神经系统疾病的个体中导致胃肠功能障碍。随着对胃肠功能障碍的研究进展到涵盖肠-脑-微生物群轴的多个组成部分,研究结果将有助于理解未来的方向,如微生物组工程和优化黏膜屏障以促进健康。