Washington University Pain Center, Washington University School of Medicine, St. Louis, MO, USA; Department of Anesthesiology, Washington University School of Medicine, St. Louis, MO, USA.
Center of Excellence in the Neurobiology of Addiction, Pain, and Emotion, Departments of Anesthesiology and Pain Medicine, and Pharmacology, University of Washington, Seattle, WA, USA.
Neuron. 2021 Jun 2;109(11):1791-1809.e11. doi: 10.1016/j.neuron.2021.04.026. Epub 2021 May 11.
Optical manipulations of genetically defined cell types have generated significant insights into the dynamics of neural circuits. While optogenetic activation has been relatively straightforward, rapid and reversible synaptic inhibition has proven more elusive. Here, we leveraged the natural ability of inhibitory presynaptic GPCRs to suppress synaptic transmission and characterize parapinopsin (PPO) as a GPCR-based opsin for terminal inhibition. PPO is a photoswitchable opsin that couples to G signaling cascades and is rapidly activated by pulsed blue light, switched off with amber light, and effective for repeated, prolonged, and reversible inhibition. PPO rapidly and reversibly inhibits glutamate, GABA, and dopamine release at presynaptic terminals. Furthermore, PPO alters reward behaviors in a time-locked and reversible manner in vivo. These results demonstrate that PPO fills a significant gap in the neuroscience toolkit for rapid and reversible synaptic inhibition and has broad utility for spatiotemporal control of inhibitory GPCR signaling cascades.
光遗传学方法对基因定义的细胞类型的操作,为神经回路的动态研究提供了重要的见解。虽然光遗传学激活相对简单、快速且可逆,但快速和可逆的突触抑制却更难实现。在这里,我们利用抑制性突触前 G 蛋白偶联受体抑制突触传递的自然能力,并将拟章鱼视蛋白 (PPO) 鉴定为一种基于 G 蛋白偶联受体的光控蛋白,用于末端抑制。PPO 是一种光转换型光控蛋白,可与 G 信号级联偶联,并可被脉冲蓝光快速激活,用琥珀光关闭,可实现重复、持续和可逆的抑制。PPO 可快速且可逆地抑制谷氨酸、GABA 和多巴胺在突触前末梢的释放。此外,PPO 以时间锁定和可逆的方式改变体内的奖励行为。这些结果表明,PPO 填补了神经科学工具包中快速和可逆的突触抑制的重要空白,并且在时空上对抑制性 G 蛋白偶联受体信号级联具有广泛的应用。