Szobota Stephanie, Gorostiza Pau, Del Bene Filippo, Wyart Claire, Fortin Doris L, Kolstad Kathleen D, Tulyathan Orapim, Volgraf Matthew, Numano Rika, Aaron Holly L, Scott Ethan K, Kramer Richard H, Flannery John, Baier Herwig, Trauner Dirk, Isacoff Ehud Y
Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA.
Neuron. 2007 May 24;54(4):535-45. doi: 10.1016/j.neuron.2007.05.010.
The ability to stimulate select neurons in isolated tissue and in living animals is important for investigating their role in circuits and behavior. We show that the engineered light-gated ionotropic glutamate receptor (LiGluR), when introduced into neurons, enables remote control of their activity. Trains of action potentials are optimally evoked and extinguished by 380 nm and 500 nm light, respectively, while intermediate wavelengths provide graded control over the amplitude of depolarization. Light pulses of 1-5 ms in duration at approximately 380 nm trigger precisely timed action potentials and EPSP-like responses or can evoke sustained depolarizations that persist for minutes in the dark until extinguished by a short pulse of approximately 500 nm light. When introduced into sensory neurons in zebrafish larvae, activation of LiGluR reversibly blocks the escape response to touch. Our studies show that LiGluR provides robust control over neuronal activity, enabling the dissection and manipulation of neural circuitry in vivo.
在离体组织和活体动物中刺激特定神经元的能力对于研究它们在神经回路和行为中的作用至关重要。我们发现,工程化的光门控离子型谷氨酸受体(LiGluR)导入神经元后,能够远程控制其活性。分别用380 nm和500 nm光可最佳地诱发和消除一连串动作电位,而中间波长则对去极化幅度提供分级控制。持续时间为1 - 5 ms、波长约为380 nm的光脉冲触发精确计时的动作电位和类兴奋性突触后电位(EPSP)反应,或者可诱发持续的去极化,这种去极化在黑暗中持续数分钟,直到被约500 nm光的短脉冲消除。当LiGluR导入斑马鱼幼虫的感觉神经元时,其激活可可逆地阻断对触摸的逃避反应。我们的研究表明,LiGluR对神经元活性提供了强大的控制,能够在体内剖析和操纵神经回路。