State Key Laboratory of Membrane Biology, Institute of Molecular Medicine, Peking-Tsinghua Center for Life Sciences, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Peking University, Beijing, China.
Department of Cognitive Sciences, Institute of Basic Medical Sciences, Beijing, China.
Nat Methods. 2017 Jul;14(7):713-719. doi: 10.1038/nmeth.4305. Epub 2017 May 29.
Developments in miniaturized microscopes have enabled visualization of brain activities and structural dynamics in animals engaging in self-determined behaviors. However, it remains a challenge to resolve activity at single dendritic spines in freely behaving animals. Here, we report the design and application of a fast high-resolution, miniaturized two-photon microscope (FHIRM-TPM) that accomplishes this goal. With a headpiece weighing 2.15 g and a hollow-core photonic crystal fiber delivering 920-nm femtosecond laser pulses, the FHIRM-TPM is capable of imaging commonly used biosensors (GFP and GCaMP6) at high spatiotemporal resolution (0.64 μm laterally and 3.35 μm axially, 40 Hz at 256 × 256 pixels for raster scanning and 10,000 Hz for free-line scanning). We demonstrate the microscope's robustness with hour-long recordings of neuronal activities at the level of spines in mice experiencing vigorous body movements.
微型显微镜的发展使得人们能够观察到动物在自主行为中大脑活动和结构动态的可视化。然而,在自由活动的动物中解析单个树突棘的活动仍然是一个挑战。在这里,我们报告了一种快速高分辨率、微型化双光子显微镜(FHIRM-TPM)的设计和应用,该显微镜实现了这一目标。FHIRM-TPM 头部重 2.15 克,空心光纤传输 920nm 飞秒激光脉冲,能够以高时空分辨率(横向 0.64μm,轴向 3.35μm,光栅扫描 40Hz,256×256 像素,自由线扫描 10000Hz)对常用的生物传感器(GFP 和 GCaMP6)进行成像。我们通过在经历剧烈身体运动的小鼠的棘突水平上进行长达一小时的神经元活动记录,证明了该显微镜的坚固性。