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钙敏和光控开关诱导激活神经元中的基因表达。

A calcium- and light-gated switch to induce gene expression in activated neurons.

机构信息

Max Planck Florida Institute for Neuroscience, Jupiter, Florida, USA.

Department of Anatomy, College of Medicine, Korea University, Seoul, Republic of Korea.

出版信息

Nat Biotechnol. 2017 Sep;35(9):858-863. doi: 10.1038/nbt.3902. Epub 2017 Jun 26.

Abstract

Despite recent advances in optogenetics, it remains challenging to manipulate gene expression in specific populations of neurons. We present a dual-protein switch system, Cal-Light, that translates neuronal-activity-mediated calcium signaling into gene expression in a light-dependent manner. In cultured neurons and brain slices, we show that Cal-Light drives expression of the reporter EGFP with high spatiotemporal resolution only in the presence of both blue light and calcium. Delivery of the Cal-Light components to the motor cortex of mice by viral vectors labels a subset of excitatory and inhibitory neurons related to learned lever-pressing behavior. By using Cal-Light to drive expression of the inhibitory receptor halorhodopsin (eNpHR), which responds to yellow light, we temporarily inhibit the lever-pressing behavior, confirming that the labeled neurons mediate the behavior. Thus, Cal-Light enables dissection of neural circuits underlying complex mammalian behaviors with high spatiotemporal precision.

摘要

尽管近年来在光遗传学方面取得了进展,但仍然难以在特定神经元群体中操纵基因表达。我们提出了一种双蛋白开关系统 Cal-Light,它将神经元活动介导的钙信号转化为光依赖性的基因表达。在培养的神经元和脑片中,我们表明 Cal-Light 仅在存在蓝光和钙的情况下,以高时空分辨率驱动报告基因 EGFP 的表达。通过病毒载体将 Cal-Light 组件递送到小鼠的运动皮层,标记与学习压杆行为相关的兴奋性和抑制性神经元亚群。通过使用 Cal-Light 驱动抑制性受体 halorhodopsin(eNpHR)的表达,该受体对黄光有反应,我们暂时抑制了压杆行为,证实标记的神经元介导了该行为。因此,Cal-Light 能够以高时空精度解析复杂的哺乳动物行为背后的神经回路。

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