Department of Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA; Memory and Brain Research Center, Baylor College of Medicine, Houston, TX 77030, USA.
Department of Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA; Memory and Brain Research Center, Baylor College of Medicine, Houston, TX 77030, USA; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Cell. 2021 Apr 1;184(7):1740-1756.e16. doi: 10.1016/j.cell.2021.02.009. Epub 2021 Mar 10.
The core symptoms of many neurological disorders have traditionally been thought to be caused by genetic variants affecting brain development and function. However, the gut microbiome, another important source of variation, can also influence specific behaviors. Thus, it is critical to unravel the contributions of host genetic variation, the microbiome, and their interactions to complex behaviors. Unexpectedly, we discovered that different maladaptive behaviors are interdependently regulated by the microbiome and host genes in the Cntnap2 model for neurodevelopmental disorders. The hyperactivity phenotype of Cntnap2 mice is caused by host genetics, whereas the social-behavior phenotype is mediated by the gut microbiome. Interestingly, specific microbial intervention selectively rescued the social deficits in Cntnap2 mice through upregulation of metabolites in the tetrahydrobiopterin synthesis pathway. Our findings that behavioral abnormalities could have distinct origins (host genetic versus microbial) may change the way we think about neurological disorders and how to treat them.
许多神经紊乱的核心症状传统上被认为是由影响大脑发育和功能的遗传变异引起的。然而,肠道微生物组作为另一个重要的变异来源,也会影响特定的行为。因此,解析宿主遗传变异、微生物组及其相互作用对复杂行为的影响至关重要。出人意料的是,我们在神经发育障碍的Cntnap2 模型中发现,不同的适应不良行为受微生物组和宿主基因的相互依存调节。Cntnap2 小鼠的多动表型是由宿主遗传决定的,而社会行为表型则由肠道微生物组介导。有趣的是,特定的微生物干预通过上调四氢生物蝶呤合成途径中的代谢物,选择性地挽救了 Cntnap2 小鼠的社交缺陷。我们的研究结果表明,行为异常可能有不同的起源(宿主遗传与微生物),这可能会改变我们对神经紊乱的看法以及治疗它们的方式。