| Literature DB >> 27798612 |
Robert Prevedel1,2,3,4, Aart J Verhoef5,6, Alejandro J Pernía-Andrade1, Siegfried Weisenburger1,7, Ben S Huang8, Tobias Nöbauer1,7, Alma Fernández5,6, Jeroen E Delcour1, Peyman Golshani8,9, Andrius Baltuska5, Alipasha Vaziri1,2,3,7.
Abstract
Although whole-organism calcium imaging in small and semi-transparent animals has been demonstrated, capturing the functional dynamics of large-scale neuronal circuits in awake behaving mammals at high speed and resolution has remained one of the main frontiers in systems neuroscience. Here we present a method based on light sculpting that enables unbiased single- and dual-plane high-speed (up to 160 Hz) calcium imaging as well as in vivo volumetric calcium imaging of a mouse cortical column (0.5 mm × 0.5 mm × 0.5 mm) at single-cell resolution and fast volume rates (3-6 Hz). We achieved this by tailoring the point-spread function of our microscope to the structures of interest while maximizing the signal-to-noise ratio using a home-built fiber laser amplifier with pulses that are synchronized to the imaging voxel speed. This enabled in vivo recording of calcium dynamics of several thousand neurons across cortical layers and in the hippocampus of awake behaving mice.Entities:
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Year: 2016 PMID: 27798612 PMCID: PMC5531274 DOI: 10.1038/nmeth.4040
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547