Super-resolution imaging of the extracellular space in living brain tissue
Super-resolution imaging of the extracellular space in living brain tissue
The extracellular space (ECS) of the brain has an extremely complex spatial organization, which has defied conventional light microscopy. Consequently, despite a marked interest in the physiological roles of brain ECS, its structure and dynamics remain largely inaccessible for experimenters. We combined 3D-STED microscopy and fluorescent labeling of the extracellular fluid to develop super-resolution shadow imaging (SUSHI) of brain ECS in living organotypic brain slices. SUSHI enables quantitative analysis of ECS structure and reveals dynamics on multiple scales in response to a variety of physiological stimuli. Because SUSHI produces sharp negative images of all cellular structures, it also enables unbiased imaging of unlabeled brain cells with respect to their anatomical context. Moreover, the extracellular labeling strategy greatly alleviates problems of photobleaching and phototoxicity associated with traditional imaging approaches. As a straightforward variant of STED microscopy, SUSHI provides unprecedented access to the structure and dynamics of live brain ECS and neuropil.
Animals, Brain/diagnostic imaging, Cell Movement, Coloring Agents/metabolism, Electrophysiological Phenomena, Epilepsy/pathology, Extracellular Space/metabolism, Female, Glutamates/metabolism, Imaging, Three-Dimensional, Male, Mice, Inbred C57BL, Neurons/physiology, Neuropil, Osmosis, Synapses/metabolism
1108-1121
Tønnesen, Jan
30c73d5c-558e-4e3a-bd4a-ada172e1211d
Inavalli, V V G Krishna
db7ab576-a272-4f04-b938-3d1772ffbd01
Nägerl, U Valentin
cbf97dc1-771a-43ae-b3c6-86f34040997b
22 February 2018
Tønnesen, Jan
30c73d5c-558e-4e3a-bd4a-ada172e1211d
Inavalli, V V G Krishna
db7ab576-a272-4f04-b938-3d1772ffbd01
Nägerl, U Valentin
cbf97dc1-771a-43ae-b3c6-86f34040997b
Tønnesen, Jan, Inavalli, V V G Krishna and Nägerl, U Valentin
(2018)
Super-resolution imaging of the extracellular space in living brain tissue.
Cell, 172 (5), , [e15].
(doi:10.1016/j.cell.2018.02.007).
Abstract
The extracellular space (ECS) of the brain has an extremely complex spatial organization, which has defied conventional light microscopy. Consequently, despite a marked interest in the physiological roles of brain ECS, its structure and dynamics remain largely inaccessible for experimenters. We combined 3D-STED microscopy and fluorescent labeling of the extracellular fluid to develop super-resolution shadow imaging (SUSHI) of brain ECS in living organotypic brain slices. SUSHI enables quantitative analysis of ECS structure and reveals dynamics on multiple scales in response to a variety of physiological stimuli. Because SUSHI produces sharp negative images of all cellular structures, it also enables unbiased imaging of unlabeled brain cells with respect to their anatomical context. Moreover, the extracellular labeling strategy greatly alleviates problems of photobleaching and phototoxicity associated with traditional imaging approaches. As a straightforward variant of STED microscopy, SUSHI provides unprecedented access to the structure and dynamics of live brain ECS and neuropil.
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Accepted/In Press date: 1 February 2018
e-pub ahead of print date: 22 February 2018
Published date: 22 February 2018
Additional Information:
Copyright © 2018 Elsevier Inc.
Keywords:
Animals, Brain/diagnostic imaging, Cell Movement, Coloring Agents/metabolism, Electrophysiological Phenomena, Epilepsy/pathology, Extracellular Space/metabolism, Female, Glutamates/metabolism, Imaging, Three-Dimensional, Male, Mice, Inbred C57BL, Neurons/physiology, Neuropil, Osmosis, Synapses/metabolism
Identifiers
Local EPrints ID: 467629
URI: http://eprints.soton.ac.uk/id/eprint/467629
ISSN: 0092-8674
PURE UUID: bda844ec-6ff1-4cf6-9a3e-6aaa95378a5f
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Date deposited: 15 Jul 2022 19:21
Last modified: 17 Mar 2024 04:04
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Author:
Jan Tønnesen
Author:
V V G Krishna Inavalli
Author:
U Valentin Nägerl
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