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A large field of view two-photon mesoscope with subcellular resolution for in vivo imaging
Imaging is used to map activity across populations of neurons. Microscopes with cellular resolution have small (<1 millimeter) fields of view and cannot simultaneously image activity distributed across multiple brain areas. Typical large field of view microscopes do not resolve single cells, espe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951199/ https://www.ncbi.nlm.nih.gov/pubmed/27300105 http://dx.doi.org/10.7554/eLife.14472 |
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author | Sofroniew, Nicholas James Flickinger, Daniel King, Jonathan Svoboda, Karel |
author_facet | Sofroniew, Nicholas James Flickinger, Daniel King, Jonathan Svoboda, Karel |
author_sort | Sofroniew, Nicholas James |
collection | PubMed |
description | Imaging is used to map activity across populations of neurons. Microscopes with cellular resolution have small (<1 millimeter) fields of view and cannot simultaneously image activity distributed across multiple brain areas. Typical large field of view microscopes do not resolve single cells, especially in the axial dimension. We developed a 2-photon random access mesoscope (2p-RAM) that allows high-resolution imaging anywhere within a volume spanning multiple brain areas (∅ 5 mm x 1 mm cylinder). 2p-RAM resolution is near diffraction limited (lateral, 0.66 μm, axial 4.09 μm at the center; excitation wavelength = 970 nm; numerical aperture = 0.6) over a large range of excitation wavelengths. A fast three-dimensional scanning system allows efficient sampling of neural activity in arbitrary regions of interest across the entire imaging volume. We illustrate the use of the 2p-RAM by imaging neural activity in multiple, non-contiguous brain areas in transgenic mice expressing protein calcium sensors. DOI: http://dx.doi.org/10.7554/eLife.14472.001 |
format | Online Article Text |
id | pubmed-4951199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49511992016-07-21 A large field of view two-photon mesoscope with subcellular resolution for in vivo imaging Sofroniew, Nicholas James Flickinger, Daniel King, Jonathan Svoboda, Karel eLife Biophysics and Structural Biology Imaging is used to map activity across populations of neurons. Microscopes with cellular resolution have small (<1 millimeter) fields of view and cannot simultaneously image activity distributed across multiple brain areas. Typical large field of view microscopes do not resolve single cells, especially in the axial dimension. We developed a 2-photon random access mesoscope (2p-RAM) that allows high-resolution imaging anywhere within a volume spanning multiple brain areas (∅ 5 mm x 1 mm cylinder). 2p-RAM resolution is near diffraction limited (lateral, 0.66 μm, axial 4.09 μm at the center; excitation wavelength = 970 nm; numerical aperture = 0.6) over a large range of excitation wavelengths. A fast three-dimensional scanning system allows efficient sampling of neural activity in arbitrary regions of interest across the entire imaging volume. We illustrate the use of the 2p-RAM by imaging neural activity in multiple, non-contiguous brain areas in transgenic mice expressing protein calcium sensors. DOI: http://dx.doi.org/10.7554/eLife.14472.001 eLife Sciences Publications, Ltd 2016-06-14 /pmc/articles/PMC4951199/ /pubmed/27300105 http://dx.doi.org/10.7554/eLife.14472 Text en © 2016, Sofroniew et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Sofroniew, Nicholas James Flickinger, Daniel King, Jonathan Svoboda, Karel A large field of view two-photon mesoscope with subcellular resolution for in vivo imaging |
title | A large field of view two-photon mesoscope with subcellular resolution for in vivo imaging |
title_full | A large field of view two-photon mesoscope with subcellular resolution for in vivo imaging |
title_fullStr | A large field of view two-photon mesoscope with subcellular resolution for in vivo imaging |
title_full_unstemmed | A large field of view two-photon mesoscope with subcellular resolution for in vivo imaging |
title_short | A large field of view two-photon mesoscope with subcellular resolution for in vivo imaging |
title_sort | large field of view two-photon mesoscope with subcellular resolution for in vivo imaging |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951199/ https://www.ncbi.nlm.nih.gov/pubmed/27300105 http://dx.doi.org/10.7554/eLife.14472 |
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