Morphological and neurochemical characterization of glycinergic neurons in laminae I-IV of the mouse spinal dorsal horn.

cell morphology glycine transporter 2 glycinergic neurons immunohistochemistry mouse spinal dorsal horn

Journal

The Journal of comparative neurology
ISSN: 1096-9861
Titre abrégé: J Comp Neurol
Pays: United States
ID NLM: 0406041

Informations de publication

Date de publication:
02 2022
Historique:
revised: 04 08 2021
received: 03 03 2021
accepted: 09 08 2021
pubmed: 13 8 2021
medline: 5 4 2022
entrez: 12 8 2021
Statut: ppublish

Résumé

A growing body of experimental evidence shows that glycinergic inhibition plays vital roles in spinal pain processing. In spite of this, however, our knowledge about the morphology, neurochemical characteristics, and synaptic relations of glycinergic neurons in the spinal dorsal horn is very limited. The lack of this knowledge makes our understanding about the specific contribution of glycinergic neurons to spinal pain processing quite vague. Here we investigated the morphology and neurochemical characteristics of glycinergic neurons in laminae I-IV of the spinal dorsal horn using a GlyT2::CreERT2-tdTomato transgenic mouse line. Confirming previous reports, we show that glycinergic neurons are sparsely distributed in laminae I-II, but their densities are much higher in lamina III and especially in lamina IV. First in the literature, we provide experimental evidence indicating that in addition to neurons in which glycine colocalizes with GABA, there are glycinergic neurons in laminae I-II that do not express GABA and can thus be referred to as glycine-only neurons. According to the shape and size of cell bodies and dendritic morphology, we divided the tdTomato-labeled glycinergic neurons into three and six morphological groups in laminae I-II and laminae III-IV, respectively. We also demonstrate that most of the glycinergic neurons co-express neuronal nitric oxide synthase, parvalbumin, the receptor tyrosine kinase RET, and the retinoic acid-related orphan nuclear receptor β (RORβ), but there might be others that need further neurochemical characterization. The present findings may foster our understanding about the contribution of glycinergic inhibition to spinal pain processing.

Identifiants

pubmed: 34382691
doi: 10.1002/cne.25232
doi:

Substances chimiques

Parvalbumins 0
Glycine TE7660XO1C

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

607-626

Subventions

Organisme : Swiss National Science Foundation
ID : 310030197888
Pays : Switzerland

Informations de copyright

© 2021 The Authors. The Journal of Comparative Neurology published by Wiley Periodicals LLC.

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Auteurs

Camila Oliveira Miranda (CO)

Department of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Krisztina Hegedüs (K)

Department of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Hendrik Wildner (H)

Institute of Pharmacology and Toxicology, University of Zurich, Zurich, Switzerland.

Hanns Ulrich Zeilhofer (HU)

Institute of Pharmacology and Toxicology, University of Zurich, Zurich, Switzerland.
Institute of Pharmaceutical Sciences, Swiss Federal Institute of Technology, Zurich, Switzerland.

Miklós Antal (M)

Department of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

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