Cargando…

Real-time 3D movement correction for two-photon imaging in behaving animals

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 artefacts are typically corrected using post-hoc processing of 2D images, but this a...

Descripción completa

Detalles Bibliográficos
Autores principales: Griffiths, Victoria A., Valera, Antoine M., Lau, Joanna YN., Roš, Hana, Younts, Thomas J., Marin, Bóris, Baragli, Chiara, Coyle, Diccon, Evans, Geoffrey J., Konstantinou, George, Koimtzis, Theo, Nadella, K. M. Naga Srinivas, Punde, Sameer A., Kirkby, Paul A., Bianco, Isaac H., Silver, R. Angus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7370269/
https://www.ncbi.nlm.nih.gov/pubmed/32483335
http://dx.doi.org/10.1038/s41592-020-0851-7
Descripción
Sumario: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 artefacts are typically corrected using post-hoc processing of 2D 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 3D laser scanning using an acousto-optic lens and rapid closed-loop FPGA 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 sub-micrometer precision.