Lin Wan-Chen, Tsai Ming-Chi, Davenport Christopher M, Smith Caleb M, Veit Julia, Wilson Neil M, Adesnik Hillel, Kramer Richard H
Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA.
Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA; Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA 94720, USA.
Neuron. 2015 Dec 2;88(5):879-891. doi: 10.1016/j.neuron.2015.10.026. Epub 2015 Nov 19.
Exogenously expressed opsins are valuable tools for optogenetic control of neurons in circuits. A deeper understanding of neural function can be gained by bringing control to endogenous neurotransmitter receptors that mediate synaptic transmission. Here we introduce a comprehensive optogenetic toolkit for controlling GABA(A) receptor-mediated inhibition in the brain. We developed a series of photoswitch ligands and the complementary genetically modified GABA(A) receptor subunits. By conjugating the two components, we generated light-sensitive versions of the entire GABA(A) receptor family. We validated these light-sensitive receptors for applications across a broad range of spatial scales, from subcellular receptor mapping to in vivo photo-control of visual responses in the cerebral cortex. Finally, we generated a knockin mouse in which the "photoswitch-ready" version of a GABA(A) receptor subunit genomically replaces its wild-type counterpart, ensuring normal receptor expression. This optogenetic pharmacology toolkit allows scalable interrogation of endogenous GABA(A) receptor function with high spatial, temporal, and biochemical precision.
外源性表达的视蛋白是对神经回路中的神经元进行光遗传学控制的宝贵工具。通过对介导突触传递的内源性神经递质受体进行控制,可以更深入地了解神经功能。在此,我们介绍一种用于控制大脑中GABA(A)受体介导的抑制作用的综合光遗传学工具包。我们开发了一系列光开关配体和互补的基因工程改造的GABA(A)受体亚基。通过将这两个组件结合起来,我们生成了整个GABA(A)受体家族的光敏感版本。我们验证了这些光敏感受体在广泛的空间尺度上的应用,从亚细胞受体定位到大脑皮层视觉反应的体内光控制。最后,我们生成了一种基因敲入小鼠,其中一个GABA(A)受体亚基的“光开关就绪”版本在基因组上取代了其野生型对应物,确保了受体的正常表达。这种光遗传学药理学工具包能够以高空间、时间和生化精度对内源性GABA(A)受体功能进行可扩展的研究。