Nardone Stefano, Elliott Evan
Faculty of Medicine, Bar Ilan University Safed, Israel.
Front Neurosci. 2016 Jul 12;10:329. doi: 10.3389/fnins.2016.00329. eCollection 2016.
Recent studies have firmly established that the etiology of autism includes both genetic and environmental components. However, we are only just beginning to elucidate the environmental factors that might be involved in the development of autism, as well as the molecular mechanisms through which they function. Mounting epidemiological and biological evidence suggest that prenatal factors that induce a more activated immune state in the mother are involved in the development of autism. In parallel, molecular studies have highlighted the role of epigenetics in brain development as a process susceptible to environmental influences and potentially causative of autism spectrum disorders (ASD). In this review, we will discuss converging evidence for a multidirectional interaction between immune system activation in the mother during pregnancy and epigenetic regulation in the brain of the fetus that may cooperate to produce an autistic phenotype. This interaction includes immune factor-induced changes in epigenetic signatures in the brain, dysregulation of epigenetic modifications specifically in genomic regions that encode immune functions, and aberrant epigenetic regulation of microglia. Overall, the interaction between immune system activation in the mother and the subsequent epigenetic dysregulation in the developing fetal brain may be a main consideration for the environmental factors that cause autism.
最近的研究已确凿证实,自闭症的病因包括遗传和环境因素。然而,我们才刚刚开始阐明可能与自闭症发展相关的环境因素,以及它们发挥作用的分子机制。越来越多的流行病学和生物学证据表明,导致母亲免疫状态更活跃的产前因素与自闭症的发展有关。与此同时,分子研究强调了表观遗传学在大脑发育中的作用,这一过程易受环境影响,并且可能是自闭症谱系障碍(ASD)的病因。在这篇综述中,我们将讨论关于孕期母亲免疫系统激活与胎儿大脑表观遗传调控之间多向相互作用的趋同证据,这种相互作用可能共同导致自闭症表型。这种相互作用包括免疫因子诱导的大脑表观遗传特征变化、特别是在编码免疫功能的基因组区域中表观遗传修饰的失调,以及小胶质细胞的异常表观遗传调控。总体而言,母亲免疫系统激活与发育中胎儿大脑随后的表观遗传失调之间的相互作用,可能是导致自闭症的环境因素的一个主要考量。