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《使用ANNINE染料和双光子显微镜进行电压成像入门》

Primer to Voltage Imaging With ANNINE Dyes and Two-Photon Microscopy.

作者信息

Kuhn Bernd, Roome Christopher J

机构信息

Okinawa Institute of Science and Technology Graduate University, Okinawa, Japan.

出版信息

Front Cell Neurosci. 2019 Jul 16;13:321. doi: 10.3389/fncel.2019.00321. eCollection 2019.

DOI:10.3389/fncel.2019.00321
PMID:31379507
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6646528/
Abstract

ANNINE-6 and ANNINE-6plus are voltage-sensitive dyes that when combined with two-photon microscopy are ideal for recording of neuronal voltages , in both bulk loaded tissue and the dendrites of single neurons. Here, we describe in detail but for a broad audience the voltage sensing mechanism of fast voltage-sensitive dyes, with a focus on ANNINE dyes, and how voltage imaging can be optimized with one-photon and two-photon excitation. Under optimized imaging conditions the key strengths of ANNINE dyes are their high sensitivity (0.5%/mV), neglectable bleaching and phototoxicity, a linear response to membrane potential, and a temporal resolution which is faster than the optical imaging devices currently used in neurobiology (order of nanoseconds). ANNINE dyes in combination with two-photon microscopy allow depth-resolved voltage imaging in bulk loaded tissue to study average membrane voltage oscillations and sensory responses. Alternatively, if ANNINE-6plus is applied internally, supra and sub threshold voltage changes can be recorded from dendrites of single neurons in awake animals. Interestingly, in our experience ANNINE-6plus labeling is impressively stable , such that voltage imaging from single Purkinje neuron dendrites can be performed for 2 weeks after a single electroporation of the neuron. Finally, to maximize their potential for neuroscience studies, voltage imaging with ANNINE dyes and two-photon microscopy can be combined with electrophysiological recording, calcium imaging, and/or pharmacology, even in awake animals.

摘要

ANNINE-6和ANNINE-6plus是电压敏感染料,与双光子显微镜结合使用时,非常适合在大量加载的组织和单个神经元的树突中记录神经元电压。在这里,我们面向广大读者详细描述了快速电压敏感染料的电压传感机制,重点是ANNINE染料,以及如何通过单光子和双光子激发优化电压成像。在优化的成像条件下,ANNINE染料的关键优势在于其高灵敏度(0.5%/mV)、可忽略不计的漂白和光毒性、对膜电位的线性响应,以及比目前神经生物学中使用的光学成像设备更快的时间分辨率(纳秒级)。ANNINE染料与双光子显微镜结合,可在大量加载的组织中进行深度分辨电压成像,以研究平均膜电压振荡和感觉反应。或者,如果将ANNINE-6plus应用于内部,可以从清醒动物单个神经元的树突中记录阈上和阈下电压变化。有趣的是,根据我们的经验,ANNINE-6plus标记非常稳定,以至于在对单个神经元进行一次电穿孔后,可在两周内对单个浦肯野神经元树突进行电压成像。最后,为了最大限度地发挥其在神经科学研究中的潜力,即使在清醒动物中,使用ANNINE染料和双光子显微镜进行电压成像也可以与电生理记录、钙成像和/或药理学相结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/53085ecccae8/fncel-13-00321-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/ebcf21643117/fncel-13-00321-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/b0fabf086ca8/fncel-13-00321-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/9b6c5689111f/fncel-13-00321-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/c65e4423ebf0/fncel-13-00321-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/cd107cf6621a/fncel-13-00321-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/53085ecccae8/fncel-13-00321-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/ebcf21643117/fncel-13-00321-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/dad1f290eeb2/fncel-13-00321-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/67107d05dc02/fncel-13-00321-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/48515bb1b9d3/fncel-13-00321-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/b0fabf086ca8/fncel-13-00321-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/9b6c5689111f/fncel-13-00321-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/c65e4423ebf0/fncel-13-00321-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/cd107cf6621a/fncel-13-00321-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c88/6646528/53085ecccae8/fncel-13-00321-g009.jpg

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