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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-8999035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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