| Literature DB >> 26687363 |
Raju Tomer1, Matthew Lovett-Barron1, Isaac Kauvar2, Aaron Andalman1, Vanessa M Burns3, Sethuraman Sankaran4, Logan Grosenick4, Michael Broxton5, Samuel Yang2, Karl Deisseroth6.
Abstract
The goal of understanding living nervous systems has driven interest in high-speed and large field-of-view volumetric imaging at cellular resolution. Light sheet microscopy approaches have emerged for cellular-resolution functional brain imaging in small organisms such as larval zebrafish, but remain fundamentally limited in speed. Here, we have developed SPED light sheet microscopy, which combines large volumetric field-of-view via an extended depth of field with the optical sectioning of light sheet microscopy, thereby eliminating the need to physically scan detection objectives for volumetric imaging. SPED enables scanning of thousands of volumes-per-second, limited only by camera acquisition rate, through the harnessing of optical mechanisms that normally result in unwanted spherical aberrations. We demonstrate capabilities of SPED microscopy by performing fast sub-cellular resolution imaging of CLARITY mouse brains and cellular-resolution volumetric Ca(2+) imaging of entire zebrafish nervous systems. Together, SPED light sheet methods enable high-speed cellular-resolution volumetric mapping of biological system structure and function.Entities:
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Year: 2015 PMID: 26687363 PMCID: PMC4775738 DOI: 10.1016/j.cell.2015.11.061
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582