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Simultaneous 2-photon calcium imaging at different cortical depths in vivo with spatiotemporal multiplexing

In vivo 2-photon calcium imaging would benefit from the use of multiple excitation beams to increase scanning speed, signal-to-noise ratio, field of view, or to image different axial planes simultaneously. We adapted a spatiotemporal multiplexing approach to circumvent the problem of light scatterin...

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Detalles Bibliográficos
Autores principales: Cheng, Adrian, Gonçalves, J. Tiago, Golshani, Peyman, Arisaka, Katsushi, Portera-Cailliau, Carlos
Formato: Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3076599/
https://www.ncbi.nlm.nih.gov/pubmed/21217749
http://dx.doi.org/10.1038/nmeth.1552
Descripción
Sumario:In vivo 2-photon calcium imaging would benefit from the use of multiple excitation beams to increase scanning speed, signal-to-noise ratio, field of view, or to image different axial planes simultaneously. We adapted a spatiotemporal multiplexing approach to circumvent the problem of light scattering ambiguity in deep tissue inherent to multifocal 2-photon microscopy. We demonstrate 2-photon calcium imaging at multiple axial planes in the in vivo mouse brain to monitor network activity of large ensembles of cortical neurons in three spatial dimensions.