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Expression of Cholinergic Markers and Characterization of Splice Variants during Ontogenesis of Rat Dorsal Root Ganglia Neurons

Dorsal root ganglia (DRG) neurons synthesize acetylcholine (ACh), in addition to their peptidergic nature. They also release ACh and are cholinoceptive, as they express cholinergic receptors. During gangliogenesis, ACh plays an important role in neuronal differentiation, modulating neuritic outgrowt...

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Autores principales: Corsetti, Veronica, Perrone-Capano, Carla, Salazar Intriago, Michael Sebastian, Botticelli, Elisabetta, Poiana, Giancarlo, Augusti-Tocco, Gabriella, Biagioni, Stefano, Tata, Ada Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197147/
https://www.ncbi.nlm.nih.gov/pubmed/34071104
http://dx.doi.org/10.3390/ijms22115499
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author Corsetti, Veronica
Perrone-Capano, Carla
Salazar Intriago, Michael Sebastian
Botticelli, Elisabetta
Poiana, Giancarlo
Augusti-Tocco, Gabriella
Biagioni, Stefano
Tata, Ada Maria
author_facet Corsetti, Veronica
Perrone-Capano, Carla
Salazar Intriago, Michael Sebastian
Botticelli, Elisabetta
Poiana, Giancarlo
Augusti-Tocco, Gabriella
Biagioni, Stefano
Tata, Ada Maria
author_sort Corsetti, Veronica
collection PubMed
description Dorsal root ganglia (DRG) neurons synthesize acetylcholine (ACh), in addition to their peptidergic nature. They also release ACh and are cholinoceptive, as they express cholinergic receptors. During gangliogenesis, ACh plays an important role in neuronal differentiation, modulating neuritic outgrowth and neurospecific gene expression. Starting from these data, we studied the expression of choline acetyltransferase (ChAT) and vesicular ACh transporter (VAChT) expression in rat DRG neurons. ChAT and VAChT genes are arranged in a “cholinergic locus”, and several splice variants have been described. Using selective primers, we characterized splice variants of these cholinergic markers, demonstrating that rat DRGs express R1, R2, M, and N variants for ChAT and V1, V2, R1, and R2 splice variants for VAChT. Moreover, by RT-PCR analysis, we observed a progressive decrease in ChAT and VAChT transcripts from the late embryonic developmental stage (E18) to postnatal P2 and P15 and in the adult DRG. Interestingly, Western blot analyses and activity assays demonstrated that ChAT levels significantly increased during DRG ontogenesis. The modulated expression of different ChAT and VAChT splice variants during development suggests a possible differential regulation of cholinergic marker expression in sensory neurons and confirms multiple roles for ACh in DRG neurons, both in the embryo stage and postnatally.
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spelling pubmed-81971472021-06-13 Expression of Cholinergic Markers and Characterization of Splice Variants during Ontogenesis of Rat Dorsal Root Ganglia Neurons Corsetti, Veronica Perrone-Capano, Carla Salazar Intriago, Michael Sebastian Botticelli, Elisabetta Poiana, Giancarlo Augusti-Tocco, Gabriella Biagioni, Stefano Tata, Ada Maria Int J Mol Sci Communication Dorsal root ganglia (DRG) neurons synthesize acetylcholine (ACh), in addition to their peptidergic nature. They also release ACh and are cholinoceptive, as they express cholinergic receptors. During gangliogenesis, ACh plays an important role in neuronal differentiation, modulating neuritic outgrowth and neurospecific gene expression. Starting from these data, we studied the expression of choline acetyltransferase (ChAT) and vesicular ACh transporter (VAChT) expression in rat DRG neurons. ChAT and VAChT genes are arranged in a “cholinergic locus”, and several splice variants have been described. Using selective primers, we characterized splice variants of these cholinergic markers, demonstrating that rat DRGs express R1, R2, M, and N variants for ChAT and V1, V2, R1, and R2 splice variants for VAChT. Moreover, by RT-PCR analysis, we observed a progressive decrease in ChAT and VAChT transcripts from the late embryonic developmental stage (E18) to postnatal P2 and P15 and in the adult DRG. Interestingly, Western blot analyses and activity assays demonstrated that ChAT levels significantly increased during DRG ontogenesis. The modulated expression of different ChAT and VAChT splice variants during development suggests a possible differential regulation of cholinergic marker expression in sensory neurons and confirms multiple roles for ACh in DRG neurons, both in the embryo stage and postnatally. MDPI 2021-05-23 /pmc/articles/PMC8197147/ /pubmed/34071104 http://dx.doi.org/10.3390/ijms22115499 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Corsetti, Veronica
Perrone-Capano, Carla
Salazar Intriago, Michael Sebastian
Botticelli, Elisabetta
Poiana, Giancarlo
Augusti-Tocco, Gabriella
Biagioni, Stefano
Tata, Ada Maria
Expression of Cholinergic Markers and Characterization of Splice Variants during Ontogenesis of Rat Dorsal Root Ganglia Neurons
title Expression of Cholinergic Markers and Characterization of Splice Variants during Ontogenesis of Rat Dorsal Root Ganglia Neurons
title_full Expression of Cholinergic Markers and Characterization of Splice Variants during Ontogenesis of Rat Dorsal Root Ganglia Neurons
title_fullStr Expression of Cholinergic Markers and Characterization of Splice Variants during Ontogenesis of Rat Dorsal Root Ganglia Neurons
title_full_unstemmed Expression of Cholinergic Markers and Characterization of Splice Variants during Ontogenesis of Rat Dorsal Root Ganglia Neurons
title_short Expression of Cholinergic Markers and Characterization of Splice Variants during Ontogenesis of Rat Dorsal Root Ganglia Neurons
title_sort expression of cholinergic markers and characterization of splice variants during ontogenesis of rat dorsal root ganglia neurons
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197147/
https://www.ncbi.nlm.nih.gov/pubmed/34071104
http://dx.doi.org/10.3390/ijms22115499
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