Extracellular vesicles released by LPS-stimulated spinal organotypic slices spread neuroinflammation into naïve slices through connexin43 hemichannel opening and astrocyte aberrant calcium dynamics.

GAP27 atomic force microscopy calcium imaging cytokine and chemokine neuroglia and inflammation

Journal

Frontiers in cellular neuroscience
ISSN: 1662-5102
Titre abrégé: Front Cell Neurosci
Pays: Switzerland
ID NLM: 101477935

Informations de publication

Date de publication:
2024
Historique:
received: 15 05 2024
accepted: 20 06 2024
medline: 26 7 2024
pubmed: 26 7 2024
entrez: 25 7 2024
Statut: epublish

Résumé

Neuroinflammation is a hallmark of multiple neurodegenerative diseases, shared by all pathological processes which primarily impact on neurons, including Central Nervous System (CNS) injuries. In reactive CNS, activated glia releases extracellular vesicles (EVs), nanosized membranous particles known to play a key role in intercellular communication. EVs mediate neuroinflammatory responses and might exacerbate tissue deterioration, ultimately influencing neurodegenerative disease progression. We treated spinal cord organotypic slices with LPS, a ligand extensively used to induce sEVs release, to mimic mild inflammatory conditions. We combine atomic force microscopy (AFM), nanoparticle tracking (NTA) and western blot (WB) analysis to validate the isolation and characterisation of sEVs. We further use immunofluorescence and confocal microscopy with live calcium imaging by GCaMP6f reporter to compare glial reactivity to treatments with sEVs when isolated from resting and LPS treated organ slices. In our study, we focus on CNS released small EVs (sEVs) and their impact on the biology of inflammatory environment. We address sEVs local signalling within the CNS tissue, in particular their involvement in inflammation spreading mechanism(s). sEVs are harvested from mouse organotypic spinal cord cultures, an in vitro model which features 3D complexity and retains spinal cord resident cells. By confocal microscopy and live calcium imaging we monitor glial responses in naïve spinal slices when exposed to sEVs isolated from resting and LPS treated organ slices. We show that sEVs, only when released during LPS neuroinflammation, recruit naïve astrocytes in the neuroinflammation cycle and we propose that such recruitment be mediated by EVs hemichannel (HC) permeability.

Identifiants

pubmed: 39049826
doi: 10.3389/fncel.2024.1433309
pmc: PMC11266295
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1433309

Informations de copyright

Copyright © 2024 Memo, Parisse, Amoriello, Pachetti, Palandri, Casalis, Ballerini and Ballerini.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

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Auteurs

Christian Memo (C)

Neuroscience Area, International School for Advanced Studies (SISSA/ISAS), Trieste, Italy.

Pietro Parisse (P)

Nanoinnovation Lab, ELETTRA Synchrotron Light Source, Basovizza, Italy.
CNR-IOM, Basovizza, Italy.

Roberta Amoriello (R)

Neuroscience Area, International School for Advanced Studies (SISSA/ISAS), Trieste, Italy.
Dipartimento di Medicina Sperimentale e Clinica, University of Florence, Firenze, Italy.

Maria Pachetti (M)

Neuroscience Area, International School for Advanced Studies (SISSA/ISAS), Trieste, Italy.

Anabela Palandri (A)

Neuroscience Area, International School for Advanced Studies (SISSA/ISAS), Trieste, Italy.

Loredana Casalis (L)

Nanoinnovation Lab, ELETTRA Synchrotron Light Source, Basovizza, Italy.

Clara Ballerini (C)

Dipartimento di Medicina Sperimentale e Clinica, University of Florence, Firenze, Italy.

Laura Ballerini (L)

Neuroscience Area, International School for Advanced Studies (SISSA/ISAS), Trieste, Italy.

Classifications MeSH