| Literature DB >> 28553965 |
Weijian Zong1,2, Runlong Wu1, Mingli Li1, Yanhui Hu1, Yijun Li1, Jinghang Li1, Hao Rong1, Haitao Wu3, Yangyang Xu1, Yang Lu1, Hongbo Jia1,4, Ming Fan2, Zhuan Zhou1, Yunfeng Zhang5, Aimin Wang5, Liangyi Chen1, Heping Cheng1.
Abstract
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.Entities:
Mesh:
Year: 2017 PMID: 28553965 DOI: 10.1038/nmeth.4305
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547