Weber-Stadlbauer U
Institute of Pharmacology and Toxicology, University of Zurich-Vetsuisse, Zurich, Switzerland.
Transl Psychiatry. 2017 May 2;7(5):e1113. doi: 10.1038/tp.2017.78.
Prenatal infection is an environmental risk factor for various brain disorders with neurodevelopmental components, including autism spectrum disorder and schizophrenia. Modeling this association in animals shows that maternal immune activation negatively affects fetal brain development and leads to the emergence of behavioral disturbances later in life. Recent discoveries in these preclinical models suggest that epigenetic modifications may be a critical molecular mechanism by which prenatal immune activation can mediate changes in brain development and functions, even across generations. This review discusses the potential epigenetic mechanisms underlying the effects of prenatal infections, thereby highlighting how infection-mediated epigenetic reprogramming may contribute to the transgenerational transmission of pathological traits. The identification of epigenetic and transgenerational mechanisms in infection-mediated neurodevelopmental disorders appears relevant to brain disorders independently of existing diagnostic classifications and may help identifying complex patterns of transgenerational disease transmission beyond genetic inheritance. The consideration of ancestral infectious histories may be of great clinical interest and may be pivotal for developing new preventive treatment strategies against infection-mediated neurodevelopmental disorders.
产前感染是包括自闭症谱系障碍和精神分裂症在内的各种具有神经发育成分的脑部疾病的环境风险因素。在动物模型中模拟这种关联表明,母体免疫激活会对胎儿大脑发育产生负面影响,并导致后期出现行为障碍。这些临床前模型的最新发现表明,表观遗传修饰可能是一种关键的分子机制,通过它产前免疫激活可以介导大脑发育和功能的变化,甚至跨代影响。本综述讨论了产前感染影响背后潜在的表观遗传机制,从而强调了感染介导的表观遗传重编程可能如何导致病理特征的跨代传递。在感染介导的神经发育障碍中鉴定表观遗传和跨代机制,似乎与脑部疾病相关,而与现有的诊断分类无关,并且可能有助于识别超越遗传继承的复杂跨代疾病传播模式。考虑祖先的感染史可能具有重大的临床意义,并且对于开发针对感染介导的神经发育障碍的新预防治疗策略可能至关重要。