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High-Speed Fluorescence Imaging and Intensity Profiling of Femtosecond-Induced Calcium Transients

机译:飞秒诱导的钙瞬变的高速荧光成像和强度分析

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摘要

We have demonstrated a combined imaging system, where the physiology of biological specimens can be imaged and profiled at 10–20 frames per second whilst undergoing femtosecond laser irradiation. Individual GH3 cells labeled with the calcium fluorophore Fluo-3 were stimulated using a counter-propagating focused femtosecond beam with respect to the imaging system. As a result of the stimulation, calcium waves can be generated in COS cells, and laser-induced calcium oscillations are initiated in the GH3 cells. Single-photon fluorescence images and intensity profiles of the targeted specimens are sampled in real-time using a modified PerkinElmer UltraView LCI microscope.
机译:我们已经展示了一种组合成像系统,可以在进行飞秒激光辐照时以每秒10-20帧的速度对生物标本的生理学进行成像和轮廓分析。相对于成像系统,使用反向传播的聚焦飞秒光束刺激了用钙荧光团Fluo-3标记的单个GH3细胞。刺激的结果是,可以在COS细胞中产生钙波,并在GH3细胞中引发激光诱导的钙振荡。使用改良的PerkinElmer UltraView LCI显微镜实时采集目标样品的单光子荧光图像和强度分布图。

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