Proportion and distribution of neurotransmitter-defined cell types in the ventral tegmental area and substantia nigra pars compacta.


Journal

bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187

Informations de publication

Date de publication:
28 Feb 2024
Historique:
pubmed: 11 3 2024
medline: 11 3 2024
entrez: 11 3 2024
Statut: epublish

Résumé

Most studies on the ventral tegmental area (VTA) and substantia nigra pars compacta (SNc) have focused on dopamine neurons and their role in processes such as motivation, learning, movement, and associated disorders. However there has been increasing attention on other VTA and SNc cell types that release GABA, glutamate, or a combination of these neurotransmitters. Yet the relative distributions and proportions of neurotransmitter-defined cell types across VTA and SNc has remained unclear. Here, we used fluorescent in situ hybridization in male and female mice to label VTA and SNc neurons that expressed mRNA encoding the canonical vesicular transporters for dopamine, GABA, or glutamate: vesicular monoamine transporter VMAT2, vesicular GABA transporter (VGAT), and vesicular glutamate transporter (VGLUT2). Within VTA, we found that no one type was particularly more abundant, instead we observed similar numbers of VMAT2+ (44%), VGAT+ (37%) and VGLUT2+ (41%) neurons. In SNc we found that a slight majority of neurons expressed VMAT2 (54%), fewer were VGAT+ (42%), and VGLUT2+ neurons were least abundant (16%). Moreover, 20% of VTA neurons and 10% of SNc neurons expressed more than one vesicular transporter, including 45% of VGLUT2 neurons. We also assessed within VTA and SNc subregions and found remarkable heterogeneity in cell-type composition. And by quantifying density across both anterior-posterior and medial-lateral axes we generated heatmaps to visualize the distribution of each cell type. Our data complement recent single-cell RNAseq studies and support a more diverse landscape of neurotransmitter-defined cell types in VTA and SNc than is typically appreciated.

Identifiants

pubmed: 38464250
doi: 10.1101/2024.02.28.582356
pmc: PMC10925288
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : BLRD VA
ID : I01 BX005782
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA036612
Pays : United States

Déclaration de conflit d'intérêts

COMPETING INTERESTS The authors declare no competing interests exist.

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Auteurs

Wiiliam S Conrad (WS)

University of California, San Diego, Department of Neurosciences, La Jolla CA, USA.

Lucie Oriol (L)

University of California, San Diego, Department of Neurosciences, La Jolla CA, USA.

Lauren Faget (L)

University of California, San Diego, Department of Neurosciences, La Jolla CA, USA.

Thomas S Hnasko (TS)

University of California, San Diego, Department of Neurosciences, La Jolla CA, USA.
Veterans Affairs San Diego Healthcare System, San Diego CA, USA.
Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase MD 20815, USA.

Classifications MeSH