Fishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, Department of Physiology, Michigan State University, Lansing, Michigan 48824, Department of Pharmacology and Toxicology, University of Buffalo, Buffalo, New York 14214, Department of Psychology, University of British Columbia, Vancouver, British Columbia, Canada, Department of Psychiatry, University of Pennsylvania Medical School, Philadelphia, Pennsylvania 19104, and Institut National de la Santé et de la Recherche Médicale, U1130, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 8246, and Université Pierre et Marie Curie, UM CR18, Sorbonne Université, Paris, France.
J Neurosci. 2014 Mar 12;34(11):3878-87. doi: 10.1523/JNEUROSCI.1787-13.2014.
Decreased medial prefrontal cortex (mPFC) neuronal activity is associated with social defeat-induced depression- and anxiety-like behaviors in mice. However, the molecular mechanisms underlying the decreased mPFC activity and its prodepressant role remain unknown. We show here that induction of the transcription factor ΔFosB in mPFC, specifically in the prelimbic (PrL) area, mediates susceptibility to stress. ΔFosB induction in PrL occurred selectively in susceptible mice after chronic social defeat stress, and overexpression of ΔFosB in this region, but not in the nearby infralimbic (IL) area, enhanced stress susceptibility. ΔFosB produced these effects partly through induction of the cholecystokinin (CCK)-B receptor: CCKB blockade in mPFC induces a resilient phenotype, whereas CCK administration into mPFC mimics the anxiogenic- and depressant-like effects of social stress. We previously found that optogenetic stimulation of mPFC neurons in susceptible mice reverses several behavioral abnormalities seen after chronic social defeat stress. Therefore, we hypothesized that optogenetic stimulation of cortical projections would rescue the pathological effects of CCK in mPFC. After CCK infusion in mPFC, we optogenetically stimulated mPFC projections to basolateral amygdala or nucleus accumbens, two subcortical structures involved in mood regulation. Stimulation of corticoamygdala projections blocked the anxiogenic effect of CCK, although no effect was observed on other symptoms of social defeat. Conversely, stimulation of corticoaccumbens projections reversed CCK-induced social avoidance and sucrose preference deficits but not anxiogenic-like effects. Together, these results indicate that social stress-induced behavioral deficits are mediated partly by molecular adaptations in mPFC involving ΔFosB and CCK through cortical projections to distinct subcortical targets.
内侧前额叶皮层(mPFC)神经元活动减少与小鼠社会挫败引起的抑郁和焦虑样行为有关。然而,mPFC 活性降低及其促抑郁作用的分子机制尚不清楚。我们在这里表明,转录因子ΔFosB 在 mPFC 中的诱导,特别是在额前皮质(PrL)区域,介导了对压力的易感性。慢性社会挫败应激后,易感性小鼠的 PrL 中选择性地诱导了ΔFosB,而该区域而非附近的下边缘皮质(IL)区域的ΔFosB 过表达增强了应激易感性。ΔFosB 通过诱导胆囊收缩素(CCK)-B 受体产生这些效应:mPFC 中的 CCKB 阻断诱导出有弹性的表型,而 CCK 给药到 mPFC 则模拟了社会应激的焦虑和抑郁样效应。我们之前发现,易感性小鼠 mPFC 神经元的光遗传学刺激可逆转慢性社会挫败应激后出现的几种行为异常。因此,我们假设光遗传学刺激皮质投射将挽救 CCK 在 mPFC 中的病理性作用。在 mPFC 中给予 CCK 输注后,我们用光遗传学刺激 mPFC 投射到外侧杏仁核或伏隔核,这两个涉及情绪调节的皮质下结构。皮质杏仁核投射的刺激阻断了 CCK 的焦虑效应,尽管对其他社会挫败症状没有影响。相反,刺激皮质伏隔核投射逆转了 CCK 诱导的社会回避和蔗糖偏好缺陷,但没有焦虑样效应。总之,这些结果表明,社会应激引起的行为缺陷部分是通过 mPFC 中涉及ΔFosB 和 CCK 的分子适应通过皮质投射到不同的皮质下靶标介导的。