Department of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Elife. 2022 Apr 25;11:e77755. doi: 10.7554/eLife.77755.
Dendritic spines are the central postsynaptic machinery that determines synaptic function. The F-actin within dendritic spines regulates their dynamic formation and elimination. Rai14 is an F-actin-regulating protein with a membrane-shaping function. Here, we identified the roles of Rai14 for the regulation of dendritic spine dynamics associated with stress-induced depressive-like behaviors. Rai14-deficient neurons exhibit reduced dendritic spine density in the mouse brain, resulting in impaired functional synaptic activity. Rai14 was protected from degradation by complex formation with Tara, and accumulated in the dendritic spine neck, thereby enhancing spine maintenance. Concurrently, Rai14 deficiency in mice altered gene expression profile relevant to depressive conditions and increased depressive-like behaviors. Moreover, Rai14 expression was reduced in the prefrontal cortex of the mouse stress model, which was blocked by antidepressant treatment. Thus, we propose that Rai14-dependent regulation of dendritic spines may underlie the plastic changes of neuronal connections relevant to depressive-like behaviors.
树突棘是决定突触功能的中枢后突触机制。树突棘内的 F-肌动蛋白调节其动态形成和消除。Rai14 是一种具有膜成形功能的 F-肌动蛋白调节蛋白。在这里,我们确定了 Rai14 在调节与应激诱导的抑郁样行为相关的树突棘动力学中的作用。Rai14 缺陷神经元在小鼠大脑中表现出树突棘密度降低,导致功能突触活性受损。Rai14 通过与 Tara 的复合物形成而免受降解,并在树突棘颈部积累,从而增强了棘突的维持。同时,小鼠 Rai14 缺失改变了与抑郁状态相关的基因表达谱,并增加了抑郁样行为。此外,应激模型中小鼠前额叶皮质中的 Rai14 表达减少,抗抑郁治疗可阻断这一现象。因此,我们提出 Rai14 依赖的树突棘调节可能是与抑郁样行为相关的神经元连接可塑性变化的基础。