Washington State University, Integrative Physiology and Neuroscience, Pullman, Washington 99164.
Washington State University, Integrative Physiology and Neuroscience, Pullman, Washington 99164
J Neurosci. 2020 Aug 5;40(32):6133-6145. doi: 10.1523/JNEUROSCI.1931-19.2020. Epub 2020 Jul 6.
The endocannabinoid system plays important roles in brain development, but mechanistic studies have focused on neuronal differentiation, migration, and synaptogenesis, with less attention to transcellular interactions that coordinate neurodevelopmental processes across developing neural networks. We determined that, in the developing rodent cerebellar cortex (of both sexes), there is a transient window when the dominant brain cannabinoid receptor, CB1R, is expressed on afferent terminals instead of output neuron Purkinje cell synapses that dominate the adult cerebellum. Activation of these afferent CB1Rs suppresses synaptic transmission onto developing granule cells, and consequently also suppresses excitation of downstream neurons in the developing cortical network, including nonsynaptic, migrating neurons. Application of a CB1R antagonist during afferent stimulation trains and depolarizing voltage steps caused a significant, sustained potentiation of synaptic amplitude. Our data demonstrate that transiently expressed afferent CB1Rs regulate afferent synaptic strength during synaptogenesis, which enables coordinated dampening of transcortical developmental signals. The endogenous cannabinoid system plays diverse roles in brain development, which, combined with the rapidly changing legal and medical status of cannabis-related compounds, makes understanding how exogenous cannabinoids affect brain development an important biomedical objective. The cerebellum is a key brain region in a variety of neurodevelopmental disorders, and the adult cerebellum has one of the highest expression levels of CB1R, but little is known about CB1R in the developing cerebellum. Here we report a developmentally distinct expression and function of CB1R in the cerebellum, in which endogenous or exogenous activation of CB1Rs modifies afferent synaptic strength and coordinated downstream network signaling. These findings have implications for recreational and medical use of exogenous cannabinoids by pregnant and breastfeeding women.
内源性大麻素系统在大脑发育中起着重要作用,但机制研究主要集中在神经元分化、迁移和突触形成上,而对跨细胞相互作用的关注较少,这些相互作用协调了发育中的神经网络中的神经发育过程。我们确定,在发育中的啮齿动物小脑皮质(雌雄同体)中,存在一个短暂的窗口,此时优势大脑大麻素受体 CB1R 表达在传入末梢上,而不是支配成年小脑的输出神经元浦肯野细胞突触上。这些传入 CB1R 的激活抑制了发育中的颗粒细胞上的突触传递,因此也抑制了发育中的皮质网络中包括非突触、迁移神经元在内的下游神经元的兴奋。在传入刺激训练和去极化电压步期间应用 CB1R 拮抗剂会导致突触幅度的显著持续增强。我们的数据表明,短暂表达的传入 CB1R 在突触发生期间调节传入突触强度,从而实现跨皮质发育信号的协调抑制。内源性大麻素系统在大脑发育中发挥着多种作用,再加上与大麻相关化合物的法律和医疗地位迅速变化,这使得了解外源性大麻素如何影响大脑发育成为一个重要的生物医学目标。小脑是多种神经发育障碍的关键脑区,成年小脑具有最高的 CB1R 表达水平之一,但对发育中小脑的 CB1R 知之甚少。在这里,我们报告了 CB1R 在小脑中的一种发育上不同的表达和功能,其中内源性或外源性激活 CB1R 可调节传入突触强度和协调的下游网络信号。这些发现对孕妇和哺乳期妇女娱乐和医疗使用外源性大麻素具有重要意义。