Department of Physiology, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
Department of Integrative Aging Neuroscience, National Center for Geriatrics and Gerontology, Aichi, 474-8511, Japan.
Sci Rep. 2017 Aug 16;7(1):8471. doi: 10.1038/s41598-017-08849-3.
Exposure to a stressful environment early in life can cause psychiatric disorders by disrupting circuit formation. Actin plays central roles in regulating neuronal structure and protein trafficking. We have recently reported that neonatal isolation inactivated ADF/cofilin, the actin depolymerizing factor, resulted in a reduced actin dynamics at spines and an attenuation of synaptic α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptor delivery in the juvenile rat medial prefrontal cortex (mPFC), leading to altered social behaviours. Here, we investigated the impact of neonatal social isolation in the developing rat barrel cortex. Similar to the mPFC study, we detected an increase in stable actin fraction in spines and this resulted in a decreased synaptic AMPA receptor delivery. Thus, we conclude that early life social isolation affects multiple cortical areas with common molecular changes.
早期生活在应激环境中会通过破坏回路形成导致精神疾病。肌动蛋白在调节神经元结构和蛋白运输中起核心作用。我们最近报道,新生期隔离会使肌动蛋白解聚因子 ADF/cofilin 失活,导致幼年大鼠内侧前额叶皮质(mPFC)中棘突的肌动蛋白动力学降低,以及突触 AMPA 受体的转运减少,从而改变社会行为。在这里,我们研究了新生期社交隔离对发育中的大鼠皮层桶状结构的影响。与 mPFC 的研究类似,我们检测到棘突中稳定肌动蛋白比例增加,这导致突触 AMPA 受体的转运减少。因此,我们得出结论,早期社交隔离会影响多个具有共同分子变化的皮质区域。