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Chronic 2P-STED imaging reveals high turnover of dendritic spines in the hippocampus in vivo

Chronic 2P-STED imaging reveals high turnover of dendritic spines in the hippocampus in vivo
Chronic 2P-STED imaging reveals high turnover of dendritic spines in the hippocampus in vivo
Rewiring neural circuits by the formation and elimination of synapses is thought to be a key cellular mechanism of learning and memory in the mammalian brain. Dendritic spines are the postsynaptic structural component of excitatory synapses, and their experience-dependent plasticity has been extensively studied in mouse superficial cortex using two-photon microscopy in vivo. By contrast, very little is known about spine plasticity in the hippocampus, which is the archetypical memory center of the brain, mostly because it is difficult to visualize dendritic spines in this deeply embedded structure with sufficient spatial resolution. We developed chronic 2P-STED microscopy in mouse hippocampus, using a ‘hippocampal window’ based on resection of cortical tissue and a long working distance objective for optical access. We observed a two-fold higher spine density than previous studies and measured a spine turnover of ~40% within 4 days, which depended on spine size. We thus provide direct evidence for a high level of structural rewiring of synaptic circuits and new insights into the structure-dynamics relationship of hippocampal spines. Having established chronic super-resolution microscopy in the hippocampus in vivo, our study enables longitudinal and correlative analyses of nanoscale neuroanatomical structures with genetic, molecular and behavioral experiments.
2050-084X
Pfeiffer, Thomas
d3d4dad0-924f-4bc2-9d95-ffc76cb861a2
Poll, Stefanie
02f0473e-5f0c-4602-b21d-5aa4f1c473db
Bancelin, Stéphane
5b55a642-db80-4845-a688-ea2a7a7dd29f
Angibaud, Julie
a31a4201-234b-4c6d-8702-8ffe732fe86a
Inavalli, Veera
db7ab576-a272-4f04-b938-3d1772ffbd01
Keppler, Kevin
73e2602c-b17e-4760-b6f1-a63971af5113
Mittag, Manuel
e3b4a2b4-f030-4eff-8aaa-6a1a162fa0c2
Fuhrmann, Martin
f763a6cc-7c3a-4874-8a16-6a2b3c829453
Nägerl, U. Valentin
cbf97dc1-771a-43ae-b3c6-86f34040997b
Pfeiffer, Thomas
d3d4dad0-924f-4bc2-9d95-ffc76cb861a2
Poll, Stefanie
02f0473e-5f0c-4602-b21d-5aa4f1c473db
Bancelin, Stéphane
5b55a642-db80-4845-a688-ea2a7a7dd29f
Angibaud, Julie
a31a4201-234b-4c6d-8702-8ffe732fe86a
Inavalli, Veera
db7ab576-a272-4f04-b938-3d1772ffbd01
Keppler, Kevin
73e2602c-b17e-4760-b6f1-a63971af5113
Mittag, Manuel
e3b4a2b4-f030-4eff-8aaa-6a1a162fa0c2
Fuhrmann, Martin
f763a6cc-7c3a-4874-8a16-6a2b3c829453
Nägerl, U. Valentin
cbf97dc1-771a-43ae-b3c6-86f34040997b

Pfeiffer, Thomas, Poll, Stefanie, Bancelin, Stéphane, Angibaud, Julie, Inavalli, Veera, Keppler, Kevin, Mittag, Manuel, Fuhrmann, Martin and Nägerl, U. Valentin (2018) Chronic 2P-STED imaging reveals high turnover of dendritic spines in the hippocampus in vivo. eLife, 7 (e34700). (doi:10.7554/elife.34700.001).

Record type: Article

Abstract

Rewiring neural circuits by the formation and elimination of synapses is thought to be a key cellular mechanism of learning and memory in the mammalian brain. Dendritic spines are the postsynaptic structural component of excitatory synapses, and their experience-dependent plasticity has been extensively studied in mouse superficial cortex using two-photon microscopy in vivo. By contrast, very little is known about spine plasticity in the hippocampus, which is the archetypical memory center of the brain, mostly because it is difficult to visualize dendritic spines in this deeply embedded structure with sufficient spatial resolution. We developed chronic 2P-STED microscopy in mouse hippocampus, using a ‘hippocampal window’ based on resection of cortical tissue and a long working distance objective for optical access. We observed a two-fold higher spine density than previous studies and measured a spine turnover of ~40% within 4 days, which depended on spine size. We thus provide direct evidence for a high level of structural rewiring of synaptic circuits and new insights into the structure-dynamics relationship of hippocampal spines. Having established chronic super-resolution microscopy in the hippocampus in vivo, our study enables longitudinal and correlative analyses of nanoscale neuroanatomical structures with genetic, molecular and behavioral experiments.

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More information

Accepted/In Press date: 5 June 2018
Published date: 22 June 2018
Additional Information: Copyright Pfeiffer et al.

Identifiers

Local EPrints ID: 467270
URI: http://eprints.soton.ac.uk/id/eprint/467270
ISSN: 2050-084X
PURE UUID: 31944369-761d-49af-92e3-6b704095a355
ORCID for Veera Inavalli: ORCID iD orcid.org/0000-0002-7100-0214

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Date deposited: 05 Jul 2022 16:32
Last modified: 17 Mar 2024 04:04

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Contributors

Author: Thomas Pfeiffer
Author: Stefanie Poll
Author: Stéphane Bancelin
Author: Julie Angibaud
Author: Veera Inavalli ORCID iD
Author: Kevin Keppler
Author: Manuel Mittag
Author: Martin Fuhrmann
Author: U. Valentin Nägerl

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