Shrestha Prerana, Mousa Awni, Heintz Nathaniel
Laboratory of Molecular Biology, Howard Hughes Medical Institute, The Rockefeller University, New York, United States.
Elife. 2015 Sep 15;4:e08752. doi: 10.7554/eLife.08752.
Major depressive disorder (MDD) is a prevalent illness that can be precipitated by acute or chronic stress. Studies of patients with Wolfram syndrome and carriers have identified Wfs1 mutations as causative for MDD. The medial prefrontal cortex (mPFC) is known to be involved in depression and behavioral resilience, although the cell types and circuits in the mPFC that moderate depressive behaviors in response to stress have not been determined. Here, we report that deletion of Wfs1 from layer 2/3 pyramidal cells impairs the ability of the mPFC to suppress stress-induced depressive behaviors, and results in hyperactivation of the hypothalamic-pituitary-adrenal axis and altered accumulation of important growth and neurotrophic factors. Our data identify superficial layer 2/3 pyramidal cells as critical for moderation of stress in the context of depressive behaviors and suggest that dysfunction in these cells may contribute to the clinical relationship between stress and depression.
重度抑郁症(MDD)是一种常见疾病,可由急性或慢性应激诱发。对患有沃尔弗拉姆综合征的患者及其携带者的研究已确定Wfs1突变是导致MDD的原因。内侧前额叶皮质(mPFC)已知与抑郁症和行为恢复力有关,尽管尚未确定mPFC中调节应激反应性抑郁行为的细胞类型和神经回路。在此,我们报告从第2/3层锥体神经元中删除Wfs1会损害mPFC抑制应激诱导的抑郁行为的能力,并导致下丘脑-垂体-肾上腺轴的过度激活以及重要生长和神经营养因子的积累改变。我们的数据表明,表层第2/3层锥体神经元对于在抑郁行为背景下调节应激至关重要,并表明这些细胞的功能障碍可能导致应激与抑郁之间的临床关联。