Super-resolution shadow imaging reveals local remodeling of astrocytic microstructures and brain extracellular space after osmotic challenge.

STED astrocyte extracellular space hypo-osmotic stress super-resolution shadow imaging synapse

Journal

Glia
ISSN: 1098-1136
Titre abrégé: Glia
Pays: United States
ID NLM: 8806785

Informations de publication

Date de publication:
06 2021
Historique:
revised: 26 02 2021
received: 16 07 2020
accepted: 03 03 2021
pubmed: 13 3 2021
medline: 10 2 2022
entrez: 12 3 2021
Statut: ppublish

Résumé

The extracellular space (ECS) plays a central role in brain physiology, shaping the time course and spread of neurochemicals, ions, and nutrients that ensure proper brain homeostasis and neuronal communication. Astrocytes are the most abundant type of glia cell in the brain, whose processes densely infiltrate the brain's parenchyma. As astrocytes are highly sensitive to changes in osmotic pressure, they are capable of exerting a potent physiological influence on the ECS. However, little is known about the spatial distribution and temporal dynamics of the ECS that surrounds astrocytes, owing mostly to a lack of appropriate techniques to visualize the ECS in live brain tissue. Mitigating this technical limitation, we applied the recent SUper-resolution SHadow Imaging technique (SUSHI) to astrocyte-labeled organotypic hippocampal brain slices, which allowed us to concurrently image the complex morphology of astrocytes and the ECS with unprecedented spatial resolution in a live experimental setting. Focusing on ring-like astrocytic microstructures in the spongiform domain, we found them to enclose sizable pools of interstitial fluid and cellular structures like dendritic spines. Upon experimental osmotic challenge, these microstructures remodeled and swelled up at the expense of the pools, effectively increasing the physical interface between astrocytic and cellular structures. Our study reveals novel facets of the dynamic microanatomical relationships between astrocytes, neuropil, and the ECS in living brain tissue, which could be of functional relevance for neuron-glia communication in a variety of (patho)physiological settings, for example, LTP induction, epileptic seizures or acute ischemic stroke, where osmotic disturbances are known to occur.

Identifiants

pubmed: 33710691
doi: 10.1002/glia.23995
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1605-1613

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

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Auteurs

Misa Arizono (M)

Interdisciplinary Institute for Neuroscience, Université de Bordeaux, Bordeaux, France.
Interdisciplinary Institute for Neuroscience, CNRS UMR 5297, Bordeaux, France.

V V G Krishna Inavalli (VVGK)

Interdisciplinary Institute for Neuroscience, Université de Bordeaux, Bordeaux, France.
Interdisciplinary Institute for Neuroscience, CNRS UMR 5297, Bordeaux, France.

Stéphane Bancelin (S)

Interdisciplinary Institute for Neuroscience, Université de Bordeaux, Bordeaux, France.
Interdisciplinary Institute for Neuroscience, CNRS UMR 5297, Bordeaux, France.

Mónica Fernández-Monreal (M)

Interdisciplinary Institute for Neuroscience, Université de Bordeaux, Bordeaux, France.
Interdisciplinary Institute for Neuroscience, CNRS UMR 5297, Bordeaux, France.
Bordeaux Imaging Center, UMS 3420, CNRS, Université de Bordeaux, US4 INSERM, Bordeaux, France.

U Valentin Nägerl (UV)

Interdisciplinary Institute for Neuroscience, Université de Bordeaux, Bordeaux, France.
Interdisciplinary Institute for Neuroscience, CNRS UMR 5297, Bordeaux, France.

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