| Literature DB >> 32483335 |
Victoria A Griffiths1, Antoine M Valera1, Joanna Yn Lau1, Hana Roš1, Thomas J Younts1, Bóris Marin1,2, Chiara Baragli1,3, Diccon Coyle1, Geoffrey J Evans1,4, George Konstantinou1,5, Theo Koimtzis1,6, K M Naga Srinivas Nadella1, Sameer A Punde1, Paul A Kirkby1, Isaac H Bianco1, R Angus Silver7.
Abstract
Two-photon microscopy is widely used to investigate brain function across multiple spatial scales. However, measurements of neural activity are compromised by brain movement in behaving animals. Brain motion-induced artifacts are typically corrected using post hoc processing of two-dimensional images, but this approach is slow and does not correct for axial movements. Moreover, the deleterious effects of brain movement on high-speed imaging of small regions of interest and photostimulation cannot be corrected post hoc. To address this problem, we combined random-access three-dimensional (3D) laser scanning using an acousto-optic lens and rapid closed-loop field programmable gate array processing to track 3D brain movement and correct motion artifacts in real time at up to 1 kHz. Our recordings from synapses, dendrites and large neuronal populations in behaving mice and zebrafish demonstrate real-time movement-corrected 3D two-photon imaging with submicrometer precision.Entities:
Mesh:
Year: 2020 PMID: 32483335 PMCID: PMC7370269 DOI: 10.1038/s41592-020-0851-7
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547