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Imaging tracks worm brains

机译:成像跟踪蠕虫的大脑

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摘要

Austria-based researchers have unveiled high speed imaging that can capture 70% of the neurons in the brain of a Caenorhabditis elegans worm simultaneously and with single neuron resolution. The two-photon excitation technique, based on a light sculpting microscope, opens new possibilities for studying the organism's nervous system and pairing brain function to brain anatomy. To date, researchers have focused on imaging single neurons and small networks within the worm but have struggled to track all neurons with a brain, trading off spatial or temporal accuracy with the size of the brain region under study. To bypass these limitations, Robert Prevedal and colleagues from the Research Institute of Molecular Pathology, Vienna, developed a wide-field two-photon light-sculpting method for volumetric fluorescent imaging, to optimise the distribution of light within a sample and boost resolution.
机译:奥地利的研究人员推出了高速成像技术,该技术可以同时捕获单个秀丽隐杆线虫蠕虫大脑中70%的神经元。基于光雕刻显微镜的双光子激发技术为研究生物体的神经系统以及将脑功能与大脑解剖结构配对提供了新的可能性。迄今为止,研究人员已经集中精力对蠕虫中的单个神经元和小型网络进行成像,但一直在努力跟踪大脑中的所有神经元,并在空间或时间准确性与所研究大脑区域的大小之间进行权衡。为了绕开这些限制,维也纳分子病理学研究所的Robert Prevedal及其同事开发了一种用于体积荧光成像的宽视野两光子光雕刻方法,以优化样品中光的分布并提高分辨率。

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