Nanoscopic distribution of VAChT and VGLUT3 in striatal cholinergic varicosities suggests colocalization and segregation of the two transporters in synaptic vesicles.

STimulated Emission Depletion microscopy (STED) acetylcholine-glutamate cotransmission scanning electron microscopy (SEM) striatal cholinergic interneurons (CINs) striatum type 3 vesicular glutamate transporter (VGLUT3) vesicular acetylcholine transporter (VAChT)

Journal

Frontiers in molecular neuroscience
ISSN: 1662-5099
Titre abrégé: Front Mol Neurosci
Pays: Switzerland
ID NLM: 101477914

Informations de publication

Date de publication:
2022
Historique:
received: 11 07 2022
accepted: 26 07 2022
entrez: 30 9 2022
pubmed: 1 10 2022
medline: 1 10 2022
Statut: epublish

Résumé

Striatal cholinergic interneurons (CINs) use acetylcholine (ACh) and glutamate (Glut) to regulate the striatal network since they express vesicular transporters for ACh (VAChT) and Glut (VGLUT3). However, whether ACh and Glut are released simultaneously and/or independently from cholinergic varicosities is an open question. The answer to that question requires the multichannel detection of vesicular transporters at the level of single synaptic vesicle (SV). Here, we used super-resolution STimulated Emission Depletion microscopy (STED) to characterize and quantify the distribution of VAChT and VGLUT3 in CINs SVs. Nearest-neighbor distances analysis between VAChT and VGLUT3-immunofluorescent spots revealed that 34% of CINs SVs contain both VAChT and VGLUT3. In addition, 40% of SVs expressed only VAChT while 26% of SVs contain only VGLUT3. These results suggest that SVs from CINs have the potential to store simultaneously or independently ACh and/or Glut. Overall, these morphological findings support the notion that CINs varicosities can signal with either ACh or Glut or both with an unexpected level of complexity.

Identifiants

pubmed: 36176961
doi: 10.3389/fnmol.2022.991732
pmc: PMC9513193
doi:

Types de publication

Journal Article

Langues

eng

Pagination

991732

Informations de copyright

Copyright © 2022 Cristofari, Desplanque, Poirel, Hébert, Dumas, Herzog, Danglot, Geny, Gilles, Geeverding, Bolte, Canette, Trichet, Fabre, Daumas, Pietrancosta, El Mestikawy and Bernard.

Déclaration de conflit d'intérêts

SDu was employed by Oramacell. The remaining 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.

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Auteurs

Paola Cristofari (P)

Sorbonne Université-CNRS UMR 8246-INSERM U1130-Neuroscience Paris Seine-Institut de Biologie Paris Seine (NPS-IBPS), Paris, France.

Mazarine Desplanque (M)

Sorbonne Université-CNRS UMR 8246-INSERM U1130-Neuroscience Paris Seine-Institut de Biologie Paris Seine (NPS-IBPS), Paris, France.

Odile Poirel (O)

Sorbonne Université-CNRS UMR 8246-INSERM U1130-Neuroscience Paris Seine-Institut de Biologie Paris Seine (NPS-IBPS), Paris, France.

Alison Hébert (A)

Sorbonne Université-CNRS UMR 8246-INSERM U1130-Neuroscience Paris Seine-Institut de Biologie Paris Seine (NPS-IBPS), Paris, France.

Sylvie Dumas (S)

Oramacell, Paris, France.

Etienne Herzog (E)

University of Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297, Bordeaux, France.

Lydia Danglot (L)

Université de Paris, Institute of Psychiatry and Neuroscience of Paris (IPNP), INSERM U1266, Membrane Traffic in Healthy & Diseased Brain, Paris, France.
Université de Paris, Institute of Psychiatry and Neuroscience of Paris (IPNP), INSERM U1266, NeurImag Imaging Facility, Paris, France.
GHU Paris Psychiatrie & Neurosciences, Paris, France.

David Geny (D)

Université de Paris, Institute of Psychiatry and Neuroscience of Paris (IPNP), INSERM U1266, NeurImag Imaging Facility, Paris, France.

Jean-François Gilles (JF)

Imaging Facility of the Institut de Biologie Paris-Seine (IBPS)-Sorbonne Université, Paris, France.

Audrey Geeverding (A)

Sorbonne Université, CNRS, Institut de Biologie Paris-Seine (IBPS), Service de Microscopie Électronique (IBPS-SME), Paris, France.

Susanne Bolte (S)

Imaging Facility of the Institut de Biologie Paris-Seine (IBPS)-Sorbonne Université, Paris, France.

Alexis Canette (A)

Sorbonne Université, CNRS, Institut de Biologie Paris-Seine (IBPS), Service de Microscopie Électronique (IBPS-SME), Paris, France.

Michaël Trichet (M)

Sorbonne Université, CNRS, Institut de Biologie Paris-Seine (IBPS), Service de Microscopie Électronique (IBPS-SME), Paris, France.

Véronique Fabre (V)

Sorbonne Université-CNRS UMR 8246-INSERM U1130-Neuroscience Paris Seine-Institut de Biologie Paris Seine (NPS-IBPS), Paris, France.

Stéphanie Daumas (S)

Sorbonne Université-CNRS UMR 8246-INSERM U1130-Neuroscience Paris Seine-Institut de Biologie Paris Seine (NPS-IBPS), Paris, France.

Nicolas Pietrancosta (N)

Sorbonne Université-CNRS UMR 8246-INSERM U1130-Neuroscience Paris Seine-Institut de Biologie Paris Seine (NPS-IBPS), Paris, France.
Sorbonne Université-CNRS UMR 7203-Laboratoire des BioMolécules, Paris, France.

Salah El Mestikawy (S)

Sorbonne Université-CNRS UMR 8246-INSERM U1130-Neuroscience Paris Seine-Institut de Biologie Paris Seine (NPS-IBPS), Paris, France.
Department of Psychiatry, Douglas Mental Health University Institute, McGill University, Montreal, QC, Canada.

Véronique Bernard (V)

Sorbonne Université-CNRS UMR 8246-INSERM U1130-Neuroscience Paris Seine-Institut de Biologie Paris Seine (NPS-IBPS), Paris, France.

Classifications MeSH