| Literature DB >> 31646030 |
Rui Liu1,2, Neil Ball1, James Brockill1, Leonard Kuan1, Daniel Millman1, Cassandra White1, Arielle Leon1, Derric Williams1, Shig Nishiwaki1, Saskia de Vries1, Josh Larkin1, David Sullivan1, Cliff Slaughterbeck1, Colin Farrell1, Peter Saggau1,3.
Abstract
We report a novel two-photon fluorescence microscope based on a fast-switching liquid crystal spatial light modulator and a pair of galvo-resonant scanners for large-scale recording of neural activity from the mammalian brain. The spatial light modulator is used to achieve fast switching between different imaging planes in multi-plane imaging and correct for intrinsic optical aberrations associated with this imaging scheme. The utilized imaging technique is capable of monitoring the neural activity from large populations of neurons with known coordinates spread across different layers of the neocortex in awake and behaving mice, regardless of the fluorescent labeling strategy. During each imaging session, all visual stimulus driven somatic activity could be recorded in the same behavior state. We observed heterogeneous response to different types of visual stimuli from ∼ 3,300 excitatory neurons reaching from layer II/III to V of the striate cortex.Entities:
Year: 2019 PMID: 31646030 PMCID: PMC6788611 DOI: 10.1364/BOE.10.005059
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732