Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA.
Methods Mol Biol. 2025;2861:97-109. doi: 10.1007/978-1-0716-4164-4_8.
Two-photon microscopy enables imaging of calcium signaling at cellular or subcellular resolution up to hundreds of microns deep in the living brain. Changes in the brightness of fluorescent calcium indicators provide a readout of calcium levels over time, affording information about neuronal activity and/or calcium-dependent subcellular signaling. Here, we describe a protocol for repeated two-photon imaging of calcium signals in mice expressing a genetically encoded calcium indicator that have been implanted with a chronic cranial window.
双光子显微镜能够在活体大脑中进行细胞或亚细胞分辨率的钙离子信号成像,深度可达数百微米。荧光钙离子指示剂的亮度变化提供了随时间变化的钙离子水平的读数,从而提供有关神经元活动和/或钙离子依赖的亚细胞信号的信息。在这里,我们描述了一种在表达遗传编码钙指示剂的小鼠中进行重复双光子钙信号成像的方案,这些小鼠已经植入了慢性颅窗。