显微镜
飞秒
双光子激发显微术
显微镜
材料科学
树突棘
帧速率
光学
激光器
生物医学工程
神经科学
生物
物理
荧光
医学
海马结构
作者
Weijian Zong,Runlong Wu,Mingli Li,Yanhui Hu,Yijun Li,Jinghang Li,Hao Rong,Haitao Wu,Yangyang Xu,Yang Lu,Hongbo Jia,Ming Fan,Zhuan Zhou,Yunfeng Zhang,Aimin Wang,Liangyi Chen,Heping Cheng
出处
期刊:Nature Methods
[Springer Nature]
日期:2017-05-29
卷期号:14 (7): 713-719
被引量:436
摘要
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.
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