Max Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA; Department of Pharmacology, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO 80045, USA.
Max Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA.
Cell Rep. 2021 May 4;35(5):109074. doi: 10.1016/j.celrep.2021.109074.
Stress adversely affects an array of cognitive functions. Although stress-related disorders are often addressed in adulthood, far less is known about how early-life stress (ELS) affects the developing brain in early postnatal periods. Here we show that ELS, induced by maternal separation, leads to synaptic alteration of layer 2/3 pyramidal neurons in the prefrontal cortex (PFC) of mice. We find that layer 2/3 neurons show increased excitatory synapse numbers following ELS and that this is accompanied by hyperexcitability of PFC-projecting dopamine (DA) neurons in the ventral tegmental area. Notably, excitatory synaptic change requires local signaling through DA D2 receptors. In vivo pharmacological treatment with a D2 receptor agonist in the PFC of control mice mimics the effects of ELS on synaptic alterations. Our findings reveal a neuromodulatory mechanism underlying ELS-induced PFC dysfunction, and this mechanism may facilitate a more comprehensive understanding of how ELS leads to mental disorders.
压力会对一系列认知功能产生不良影响。尽管与压力相关的疾病通常在成年期得到解决,但人们对早期生活压力 (ELS) 如何在出生后早期影响发育中的大脑知之甚少。在这里,我们表明,由母体分离引起的 ELS 会导致前额叶皮层 (PFC) 中 2/3 层锥体神经元的突触改变。我们发现,ELS 后 2/3 层神经元的兴奋性突触数量增加,并且伴随着腹侧被盖区中投射到 PFC 的多巴胺 (DA) 神经元的过度兴奋。值得注意的是,兴奋性突触变化需要通过 DA D2 受体进行局部信号转导。在控制小鼠的 PFC 中进行体内药理学治疗,用 D2 受体激动剂模拟 ELS 对突触改变的影响。我们的研究结果揭示了 ELS 诱导的 PFC 功能障碍的神经调节机制,这一机制可能有助于更全面地了解 ELS 如何导致精神障碍。