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TRPV2: A Key Player in Myelination Disorders of the Central Nervous System

Transient potential receptor vanilloid 2 (TRPV2) is widely expressed through the nervous system and specifically found in neuronal subpopulations and some glial cells. TRPV2 is known to be sensitized by methionine oxidation, which results from inflammation. Here we aim to characterize the expression...

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Autores principales: Enrich-Bengoa, Jennifer, Manich, Gemma, Valente, Tony, Sanchez-Molina, Paula, Almolda, Beatriz, Solà, Carme, Saura, Josep, González, Berta, Castellano, Bernardo, Perálvarez-Marín, Alex
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8999035/
https://www.ncbi.nlm.nih.gov/pubmed/35408977
http://dx.doi.org/10.3390/ijms23073617
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author Enrich-Bengoa, Jennifer
Manich, Gemma
Valente, Tony
Sanchez-Molina, Paula
Almolda, Beatriz
Solà, Carme
Saura, Josep
González, Berta
Castellano, Bernardo
Perálvarez-Marín, Alex
author_facet Enrich-Bengoa, Jennifer
Manich, Gemma
Valente, Tony
Sanchez-Molina, Paula
Almolda, Beatriz
Solà, Carme
Saura, Josep
González, Berta
Castellano, Bernardo
Perálvarez-Marín, Alex
author_sort Enrich-Bengoa, Jennifer
collection PubMed
description Transient potential receptor vanilloid 2 (TRPV2) is widely expressed through the nervous system and specifically found in neuronal subpopulations and some glial cells. TRPV2 is known to be sensitized by methionine oxidation, which results from inflammation. Here we aim to characterize the expression and regulation of TRPV2 in myelination pathologies, such as hypomyelination and demyelination. We validated the interaction between TRPV2 and its putative interactor Opalin, an oligodendrocyte marker, in mixed glial cultures under pro- and anti-inflammatory conditions. Then, we characterized TRPV2 time-course expression in experimental animal models of hypomyelination (jimpy mice) and de-/remyelination (cuprizone intoxication and experimental autoimmune encephalomyelitis (EAE)). TRPV2 showed upregulation associated with remyelination, inflammation in cuprizone and EAE models, and downregulation in hypomyelinated jimpy mice. TRPV2 expression was altered in human samples of multiple sclerosis (MS) patients. Additionally, we analyzed the expression of methionine sulfoxide reductase A (MSRA), an enzyme that reduces oxidated methionines in TRPV2, which we found increased in inflammatory conditions. These results suggest that TRPV2 may be a key player in myelination in accordance with the recapitulation hypothesis, and that it may become an interesting clinical target in the treatment of demyelination disorders.
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spelling pubmed-89990352022-04-12 TRPV2: A Key Player in Myelination Disorders of the Central Nervous System Enrich-Bengoa, Jennifer Manich, Gemma Valente, Tony Sanchez-Molina, Paula Almolda, Beatriz Solà, Carme Saura, Josep González, Berta Castellano, Bernardo Perálvarez-Marín, Alex Int J Mol Sci Article Transient potential receptor vanilloid 2 (TRPV2) is widely expressed through the nervous system and specifically found in neuronal subpopulations and some glial cells. TRPV2 is known to be sensitized by methionine oxidation, which results from inflammation. Here we aim to characterize the expression and regulation of TRPV2 in myelination pathologies, such as hypomyelination and demyelination. We validated the interaction between TRPV2 and its putative interactor Opalin, an oligodendrocyte marker, in mixed glial cultures under pro- and anti-inflammatory conditions. Then, we characterized TRPV2 time-course expression in experimental animal models of hypomyelination (jimpy mice) and de-/remyelination (cuprizone intoxication and experimental autoimmune encephalomyelitis (EAE)). TRPV2 showed upregulation associated with remyelination, inflammation in cuprizone and EAE models, and downregulation in hypomyelinated jimpy mice. TRPV2 expression was altered in human samples of multiple sclerosis (MS) patients. Additionally, we analyzed the expression of methionine sulfoxide reductase A (MSRA), an enzyme that reduces oxidated methionines in TRPV2, which we found increased in inflammatory conditions. These results suggest that TRPV2 may be a key player in myelination in accordance with the recapitulation hypothesis, and that it may become an interesting clinical target in the treatment of demyelination disorders. MDPI 2022-03-25 /pmc/articles/PMC8999035/ /pubmed/35408977 http://dx.doi.org/10.3390/ijms23073617 Text en © 2022 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 Article
Enrich-Bengoa, Jennifer
Manich, Gemma
Valente, Tony
Sanchez-Molina, Paula
Almolda, Beatriz
Solà, Carme
Saura, Josep
González, Berta
Castellano, Bernardo
Perálvarez-Marín, Alex
TRPV2: A Key Player in Myelination Disorders of the Central Nervous System
title TRPV2: A Key Player in Myelination Disorders of the Central Nervous System
title_full TRPV2: A Key Player in Myelination Disorders of the Central Nervous System
title_fullStr TRPV2: A Key Player in Myelination Disorders of the Central Nervous System
title_full_unstemmed TRPV2: A Key Player in Myelination Disorders of the Central Nervous System
title_short TRPV2: A Key Player in Myelination Disorders of the Central Nervous System
title_sort trpv2: a key player in myelination disorders of the central nervous system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8999035/
https://www.ncbi.nlm.nih.gov/pubmed/35408977
http://dx.doi.org/10.3390/ijms23073617
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