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Maternal immune activation transgenerationally modulates maternal care and offspring depression-like behavior

机译:母体免疫活化转基因调节母体护理和后代抑郁症的行为

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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.
机译:越来越多地认识到妊娠感染,其参与是由于严重发育脑异常的致病机制及其对生命后期后精神病理学发病机制的贡献。基于病毒模拟多胞苷的全身施用(Poly(I:C))的全身施用,在普遍接受的母体免疫激活(MIA)模型中的首次观察最近建议跨越几代人的行为和转录性状传播。虽然母体护理行为(MCB)被称为对后代脑功能和行为对环境挑战的转基因影响的基本介质,但尚未检查由MIA引起的MIA引起的MCB改变的繁殖。在这里,我们表明聚(I:c)12.5(E12.5)在胚胎第12.5天(E12.5)刺激导致异常MCB,并且这种效果被传递给女F1后代。 MCB对MCB的转基因效应通过增强的抑郁症和第二代F2后代的行为平行,具有母体和父母遗产的贡献。检查称为MCB靶标的基因的后代海马表达,以及用于随后改变脑功能的非遗传传播和行为的相关性揭示了F1和F2代的转基因保守和修饰的表达模式。

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