海马结构
显微镜
临床前影像学
运动前神经元活动
双光子激发显微术
脑功能
时间分辨率
分辨率(逻辑)
体内
神经影像学
生物
神经科学
生物物理学
光学
物理
荧光
计算机科学
生物技术
人工智能
作者
Dimitre G. Ouzounov,Tianyu Wang,Mengran Wang,Danielle D. Feng,Nicholas G. Horton,Jean C. Cruz Hernández,Yu‐Ting Cheng,Jacob Reimer,Andreas Savas Tolias,Nozomi Nishimura,Chris Xu
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2017-02-20
卷期号:14 (4): 388-390
被引量:514
摘要
High-resolution optical imaging is critical to understanding brain function. We demonstrate that three-photon microscopy at 1,300-nm excitation enables functional imaging of GCaMP6s-labeled neurons beyond the depth limit of two-photon microscopy. We record spontaneous activity from up to 150 neurons in the hippocampal stratum pyramidale at ∼1-mm depth within an intact mouse brain. Our method creates opportunities for noninvasive recording of neuronal activity with high spatial and temporal resolution deep within scattering brain tissues.
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