Department of Neurophysiology and Neuropharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, Austria.
Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Austria.
Brain Behav Immun. 2017 Jul;63:127-136. doi: 10.1016/j.bbi.2016.10.016. Epub 2016 Oct 17.
Gestational infection is increasingly being recognized for its involvement as causative mechanism in severe developmental brain abnormalities and its contribution to the pathogenesis of psychopathologies later in life. First observations in the widely accepted maternal immune activation (MIA) model based upon the systemic administration of the viral mimetic Polyinosinic:polycytidylic acid (poly(I:C)) have recently suggested a transmission of behavioral and transcriptional traits across generations. Although maternal care behavior (MCB) is known as essential mediator of the transgenerational effects of environmental challenges on offspring brain function and behavior, the possible propagation of alterations of MCB resulting from MIA to following generations has not yet been examined. Here we show that poly(I:C) stimulation at embryonic day 12.5 (E12.5) leads to aberrant MCB and that this effect is transmitted to the female F1 offspring. The transgenerational effects on MCB are paralleled by enhanced depression-like behavior in the second generation F2 offspring with contributions of both maternal and paternal heritages. Examination of offspring hippocampal expression of genes known as targets of MCB and relevant for ensuing non-genetic transmission of altered brain function and behavior revealed transgenerationally conserved and modified expressional patterns in the F1 and F2 generation. Collectively these data firstly demonstrate the transgenerational transmission of the impact of gestational immune activation on the reproductive care behavior of the mother. Behavioral and molecular characteristics of first and second generation offspring suggest transgenerationally imprinted consequences of gestational infection on psychopathological traits related to mood disorders which remain to be examined in future cross-fostering experiments.
妊娠期感染越来越被认为是导致严重发育性脑异常的致病机制,并导致生命后期精神病理学的发病机制。最近,在广泛接受的母体免疫激活(MIA)模型中首次观察到,该模型基于全身给予病毒模拟物聚肌胞苷酸(poly(I:C)),提示行为和转录特征在代际间传递。尽管母体照顾行为(MCB)被认为是环境挑战对子代大脑功能和行为的跨代影响的重要介导者,但 MIA 导致的 MCB 改变是否会传递给后代尚未得到检验。在这里,我们表明,在胚胎第 12.5 天(E12.5)刺激 poly(I:C)会导致异常的 MCB,并且这种效应会传递给雌性 F1 后代。对 MCB 的跨代影响与第二代 F2 后代的抑郁样行为增强平行,这与母体和父系遗传都有关系。检查后代海马体中已知作为 MCB 靶点的基因的表达,这些基因与改变的大脑功能和行为的非遗传传递有关,结果显示 F1 和 F2 代中存在跨代保守和修饰的表达模式。这些数据首次证明了妊娠期免疫激活对母亲生殖照顾行为的影响的跨代传递。第一代和第二代后代的行为和分子特征表明,妊娠期感染对与情绪障碍相关的精神病理学特征具有跨代印记的后果,这有待在未来的交叉寄养实验中进一步研究。