Fast widefield imaging of neuronal structure and function with optical sectioning in vivo

Li, Ziwei; Zhang, Qinrong; Chou, Shih-Wei; Newman, Zachary; Turcotte, Raphaël; Natan, Ryan; Dai, Qionghai; Isacoff, Ehud Y.; Ji, Na

doi:10.1126/sciadv.aaz3870

Title: Fast widefield imaging of neuronal structure and function with optical sectioning in vivo

Journal Article · Fri May 08 00:00:00 EDT 2020 · Science Advances

DOI:https://doi.org/10.1126/sciadv.aaz3870· OSTI ID:1816006

^[1];

^[2]; Chou, Shih-Wei ^[3];

^[3];

^[2];

^[2]; Dai, Qionghai ^[4]; Isacoff, Ehud Y. ^[5];

^[6]

Univ. of California, Berkeley, CA (United States). Dept. of Physics; Tsinghua Univ., Beijing (China). Dept. of Automation
Univ. of California, Berkeley, CA (United States). Dept. of Physics
Univ. of California, Berkeley, CA (United States). Dept. of Molecular and Cell Biology
Tsinghua Univ., Beijing (China). Dept. of Automation
Univ. of California, Berkeley, CA (United States). Dept. of Molecular and Cell Biology and Helen Wills Neuroscience Inst.; Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Bioscience Division
Univ. of California, Berkeley, CA (United States). Dept. of Physics, Dept. of Molecular and Cell Biology and Helen Wills Neuroscience Inst.; Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Molecular Biophysics and Integrated Bioimaging Division

Optical microscopy, owing to its noninvasiveness and subcellular resolution, enables in vivo visualization of neuronal structure and function in the physiological context. Optical-sectioning structured illumination microscopy (OS-SIM) is a widefield fluorescence imaging technique that uses structured illumination patterns to encode in-focus structures and optically sections 3D samples. However, its application to in vivo imaging has been limited. In this study, we optimized OS-SIM for in vivo neural imaging. We modified OS-SIM reconstruction algorithms to improve signal-to-noise ratio and correct motion-induced artifacts in live samples. Incorporating an adaptive optics (AO) module to OS-SIM, we found that correcting sample-induced optical aberrations was essential for achieving accurate structural and functional characterizations in vivo. With AO OS-SIM, we demonstrated fast, high-resolution in vivo imaging with optical sectioning for structural imaging of mouse cortical neurons and zebrafish larval motor neurons, and functional imaging of quantal synaptic transmission at Drosophila larval neuromuscular junctions.

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Research Organization:: Univ. of California, Berkeley, CA (United States)

Sponsoring Organization:: USDOE Office of Science (SC)

Grant/Contract Number:: AC02-05CH11231

OSTI ID:: 1816006

Journal Information:: Science Advances, Vol. 6, Issue 19; ISSN 2375-2548

Publisher:: AAASCopyright Statement

Country of Publication:: United States

Language:: English

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