Allen Institute for Brain Science, Seattle, United States.
Elife. 2020 Nov 6;9:e59841. doi: 10.7554/eLife.59841.
Widefield fluorescence microscopy is used to monitor the spiking of populations of neurons in the brain. Widefield fluorescence can originate from indicator molecules at all depths in cortex and the relative contributions from somata, dendrites, and axons are often unknown. Here, I simulate widefield illumination and fluorescence collection and determine the main sources of fluorescence for several GCaMP mouse lines. Scattering strongly affects illumination and collection. One consequence is that illumination intensity is greatest ~300-400 µm below the pia, not at the brain surface. Another is that fluorescence from a source deep in cortex may extend across a diameter of 3-4 mm at the brain surface, severely limiting lateral resolution. In many mouse lines, the volume of tissue contributing to fluorescence extends through the full depth of cortex and fluorescence at most surface locations is a weighted average across multiple cortical columns and often more than one cortical area.
宽场荧光显微镜用于监测大脑中神经元群体的尖峰活动。宽场荧光可以源自皮质中所有深度的指示剂分子,而胞体、树突和轴突的相对贡献通常是未知的。在这里,我模拟了宽场照明和荧光采集,并确定了几种 GCaMP 小鼠品系的荧光主要来源。强烈的散射会影响照明和收集。一个结果是,照明强度在软脑膜下约 300-400 µm 处最大,而不是在脑表面。另一个结果是来自皮质深处的荧光可能在脑表面延伸 3-4 毫米的直径,严重限制了横向分辨率。在许多小鼠品系中,对荧光有贡献的组织体积贯穿整个皮质深度,在大多数表面位置的荧光是多个皮质柱的加权平均值,并且通常超过一个皮质区域。