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High-throughput synapse-resolving two-photon fluorescence microendoscopy for deep-brain volumetric imaging in vivo
Optical imaging has become a powerful tool for studying brains in vivo. The opacity of adult brains makes microendoscopy, with an optical probe such as a gradient index (GRIN) lens embedded into brain tissue to provide optical relay, the method of choice for imaging neurons and neural activity in de...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6338462/ https://www.ncbi.nlm.nih.gov/pubmed/30604680 http://dx.doi.org/10.7554/eLife.40805 |
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author | Meng, Guanghan Liang, Yajie Sarsfield, Sarah Jiang, Wan-chen Lu, Rongwen Dudman, Joshua Tate Aponte, Yeka Ji, Na |
author_facet | Meng, Guanghan Liang, Yajie Sarsfield, Sarah Jiang, Wan-chen Lu, Rongwen Dudman, Joshua Tate Aponte, Yeka Ji, Na |
author_sort | Meng, Guanghan |
collection | PubMed |
description | Optical imaging has become a powerful tool for studying brains in vivo. The opacity of adult brains makes microendoscopy, with an optical probe such as a gradient index (GRIN) lens embedded into brain tissue to provide optical relay, the method of choice for imaging neurons and neural activity in deeply buried brain structures. Incorporating a Bessel focus scanning module into two-photon fluorescence microendoscopy, we extended the excitation focus axially and improved its lateral resolution. Scanning the Bessel focus in 2D, we imaged volumes of neurons at high-throughput while resolving fine structures such as synaptic terminals. We applied this approach to the volumetric anatomical imaging of dendritic spines and axonal boutons in the mouse hippocampus, and functional imaging of GABAergic neurons in the mouse lateral hypothalamus in vivo. |
format | Online Article Text |
id | pubmed-6338462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63384622019-01-24 High-throughput synapse-resolving two-photon fluorescence microendoscopy for deep-brain volumetric imaging in vivo Meng, Guanghan Liang, Yajie Sarsfield, Sarah Jiang, Wan-chen Lu, Rongwen Dudman, Joshua Tate Aponte, Yeka Ji, Na eLife Neuroscience Optical imaging has become a powerful tool for studying brains in vivo. The opacity of adult brains makes microendoscopy, with an optical probe such as a gradient index (GRIN) lens embedded into brain tissue to provide optical relay, the method of choice for imaging neurons and neural activity in deeply buried brain structures. Incorporating a Bessel focus scanning module into two-photon fluorescence microendoscopy, we extended the excitation focus axially and improved its lateral resolution. Scanning the Bessel focus in 2D, we imaged volumes of neurons at high-throughput while resolving fine structures such as synaptic terminals. We applied this approach to the volumetric anatomical imaging of dendritic spines and axonal boutons in the mouse hippocampus, and functional imaging of GABAergic neurons in the mouse lateral hypothalamus in vivo. eLife Sciences Publications, Ltd 2019-01-04 /pmc/articles/PMC6338462/ /pubmed/30604680 http://dx.doi.org/10.7554/eLife.40805 Text en © 2019, Meng et al http://creativecommons.org/licenses/by/4.0/ 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 | Neuroscience Meng, Guanghan Liang, Yajie Sarsfield, Sarah Jiang, Wan-chen Lu, Rongwen Dudman, Joshua Tate Aponte, Yeka Ji, Na High-throughput synapse-resolving two-photon fluorescence microendoscopy for deep-brain volumetric imaging in vivo |
title | High-throughput synapse-resolving two-photon fluorescence microendoscopy for deep-brain volumetric imaging in vivo |
title_full | High-throughput synapse-resolving two-photon fluorescence microendoscopy for deep-brain volumetric imaging in vivo |
title_fullStr | High-throughput synapse-resolving two-photon fluorescence microendoscopy for deep-brain volumetric imaging in vivo |
title_full_unstemmed | High-throughput synapse-resolving two-photon fluorescence microendoscopy for deep-brain volumetric imaging in vivo |
title_short | High-throughput synapse-resolving two-photon fluorescence microendoscopy for deep-brain volumetric imaging in vivo |
title_sort | high-throughput synapse-resolving two-photon fluorescence microendoscopy for deep-brain volumetric imaging in vivo |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6338462/ https://www.ncbi.nlm.nih.gov/pubmed/30604680 http://dx.doi.org/10.7554/eLife.40805 |
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