神经元成像在8位深度结合高空间和高时间分辨率与采集率高达40 kHz。

Fatima Abbas, Ömer Yusuf İpek, Philippe Moreau, Marco Canepari
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引用次数: 0

摘要

从尽可能多的像素中获取高时间分辨率的帧序列是神经成像的一个挑战。测量1%-10%的荧光变化通常需要12位或更高的位深度,这限制了帧大小,允许在kHz范围内成像。我们通过获取8位深度的荧光和离线像素,在脑切片中从细胞群或单个神经元中分离Ca2+或膜电位信号,以kHz速率实现前所未有的帧大小。在用Ca2+指示剂Fluo-4 AM染色的海马切片中,我们从大帧中分辨出2 kHz的瞬态。沿着第5层锥体神经元的顶端树突,我们测量了与10 kHz反向传播动作电位相关的Ca2+信号。最后,在同一细胞类型的轴突起始段,我们用电压敏感染料成像记录了40 kHz的动作电位。这种方法开启了一系列成像测量的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuronal Imaging at 8-Bit Depth to Combine High Spatial and High Temporal Resolution With Acquisition Rates Up To 40 kHz.

A challenge in neuroimaging is acquiring frame sequences at high temporal resolution from the largest possible number of pixels. Measuring 1%-10% fluorescence changes normally requires 12-bit or higher bit depth, constraining the frame size allowing imaging in the kHz range. We resolved Ca2+ or membrane potential signals from cell populations or single neurons in brain slices by acquiring fluorescence at 8-bit depth and by binning pixels offline, achieving unprecedented frame sizes at kHz rates. In hippocampal slices stained with the Ca2+ indicator Fluo-4 AM, we resolved transients at 2 kHz from large frames. Along the apical dendrite of a layer-5 pyramidal neuron, we measured Ca2+ signals associated with a back-propagating action potential at 10 kHz. Finally, in the axon initial segment of the same cell type, we recorded an action potential at 40 kHz by voltage-sensitive dye imaging. This approach unlocks the potential for a range of imaging measurements.

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