显微镜
多光子荧光显微镜
薄层荧光显微镜
荧光显微镜
光学
神经科学
生物
扫描共焦电子显微镜
物理
荧光
作者
Robert Prevedel,Young-Gyu Yoon,Maximilian Hoffmann,Nikita Pak,Gordon Wetzstein,Saul Kato,Tina Schrödel,Ramesh Raskar,Manuel Zimmer,Edward S. Boyden,Alipasha Vaziri
出处
期刊:Nature Methods
[Springer Nature]
日期:2014-05-18
卷期号:11 (7): 727-730
被引量:715
摘要
3D functional imaging of neuronal activity in entire organisms at single cell level and physiologically relevant time scales faces major obstacles due to trade-offs between the size of the imaged volumes, and spatial and temporal resolution. Here, using light-field microscopy in combination with 3D deconvolution, we demonstrate intrinsically simultaneous volumetric functional imaging of neuronal population activity at single neuron resolution for an entire organism, the nematode Caenorhabditis elegans. The simplicity of our technique and possibility of the integration into epi-fluoresence microscopes makes it an attractive tool for high-speed volumetric calcium imaging.
科研通智能强力驱动
Strongly Powered by AbleSci AI