Kirschen Gregory W, Shen Jia, Tian Mu, Schroeder Bryce, Wang Jia, Man Guoming, Wu Song, Ge Shaoyu
Medical Scientist Training Program.
Molecular and Cellular Pharmacology Program.
J Neurosci. 2017 May 3;37(18):4661-4678. doi: 10.1523/JNEUROSCI.3417-16.2017. Epub 2017 Apr 3.
The continuous addition of new dentate granule cells (DGCs), which is regulated exquisitely by brain activity, renders the hippocampus plastic. However, how neural circuits encode experiences to affect the addition of adult-born neurons remains unknown. Here, we used endoscopic Ca imaging to track the real-time activity of individual DGCs in freely behaving mice. For the first time, we found that active DGCs responded to a novel experience by increasing their Ca event frequency preferentially. This elevated activity, which we found to be associated with object exploration, returned to baseline by 1 h in the same environment, but could be dishabituated via introduction to a novel environment. To transition seamlessly between environments, we next established a freely controllable virtual reality system for unrestrained mice. We again observed increased firing of active neurons in a virtual enriched environment. Interestingly, multiple novel virtual experiences increased the number of newborn neurons accumulatively compared with a single experience. Finally, optogenetic silencing of existing DGCs during novel environmental exploration perturbed experience-induced neuronal addition. Our study shows that the adult brain conveys novel, enriched experiences to increase the addition of adult-born hippocampal neurons by increasing the firing of active DGCs. Adult brains are constantly reshaping themselves from synapses to circuits as we encounter novel experiences from moment to moment. Importantly, this reshaping includes the addition of newborn hippocampal neurons. However, it remains largely unknown how our circuits encode experience-induced brain activity to govern the addition of new hippocampal neurons. By coupling Ca imaging of dentate granule neurons with a novel, unrestrained virtual reality system for rodents, we discovered that a new experience increased firing of active dentate granule neurons rapidly and robustly. Exploration in multiple novel virtual environments, compared with a single environment, promoted dentate activation and enhanced the addition of new hippocampal neurons accumulatively. Finally, silencing this activation optogenetically during novel experiences perturbed experience-induced neuronal addition.
新齿状颗粒细胞(DGCs)的持续添加受到大脑活动的精确调控,这使得海马体具有可塑性。然而,神经回路如何编码经验以影响成年后新生神经元的添加仍不清楚。在这里,我们使用内窥镜钙成像技术来追踪自由活动小鼠中单个DGCs的实时活动。我们首次发现,活跃的DGCs通过优先增加其钙事件频率来对新体验做出反应。我们发现这种增强的活动与物体探索有关,在同一环境中1小时内恢复到基线水平,但通过引入新环境可以使其去习惯化。为了在不同环境之间无缝过渡,我们接下来为不受约束的小鼠建立了一个可自由控制的虚拟现实系统。我们再次观察到在虚拟丰富环境中活跃神经元的放电增加。有趣的是,与单一体验相比,多种新的虚拟体验会累积增加新生神经元的数量。最后,在新环境探索期间对现有DGCs进行光遗传学沉默会干扰经验诱导的神经元添加。我们的研究表明,成年大脑通过增加活跃DGCs的放电来传递新的、丰富的体验,从而增加成年后出生的海马体神经元的添加。随着我们时刻遇到新的体验,成年大脑不断地从突触到回路进行自我重塑。重要的是,这种重塑包括新生海马体神经元的添加。然而,我们的神经回路如何编码经验诱导的大脑活动以控制新海马体神经元的添加在很大程度上仍然未知。通过将齿状颗粒神经元的钙成像与一种用于啮齿动物的新型、不受约束的虚拟现实系统相结合,我们发现新体验会迅速而强烈地增加活跃齿状颗粒神经元的放电。与单一环境相比,在多个新的虚拟环境中进行探索会促进齿状激活,并累积增强新海马体神经元的添加。最后,在新体验期间通过光遗传学沉默这种激活会干扰经验诱导的神经元添加。