Division of Neuropsychiatry, Department of Neuroscience, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube, Yamaguchi 755-8505, Japan.
Neuron. 2011 Jan 27;69(2):359-72. doi: 10.1016/j.neuron.2010.12.023.
Stressful events during adulthood are potent adverse environmental factors that can predispose individuals to psychiatric disorders, including depression; however, many individuals exposed to stressful events can adapt and function normally. While stress vulnerability may influence depression, the molecular mechanisms underlying the susceptibility and adaptation to chronic stress within the brain are poorly understood. In this study, two genetically distinct mouse strains that exhibit different behavioral responses to chronic stress were used to demonstrate how the differential epigenetic status of the glial cell-derived neurotrophic factor (Gdnf) gene in the ventral striatum modulates susceptibility and adaptation to chronic stress. Our results suggest that the histone modifications and DNA methylation of the Gdnf promoter have crucial roles in the control of behavioral responses to chronic stress. Our data provide insights into these mechanisms, suggesting that epigenetic modifications of Gdnf, along with genetic and environmental factors, contribute to behavioral responses to stress.
成年期的应激事件是潜在的不利环境因素,可使个体易患精神障碍,包括抑郁症;然而,许多接触应激事件的个体能够适应并正常运作。虽然应激易感性可能会影响抑郁症,但大脑中对慢性应激的敏感性和适应性的分子机制尚不清楚。在这项研究中,使用了两种具有不同的慢性应激行为反应的遗传上不同的小鼠品系,以证明腹侧纹状体中胶质细胞源性神经营养因子(Gdnf)基因的差异表观遗传状态如何调节对慢性应激的敏感性和适应性。我们的结果表明,Gdnf 启动子的组蛋白修饰和 DNA 甲基化在控制慢性应激的行为反应中起着关键作用。我们的数据提供了这些机制的深入了解,表明 Gdnf 的表观遗传修饰以及遗传和环境因素,有助于对压力的行为反应。