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CB(1) receptor activation induces intracellular Ca(2+) mobilization and 2-arachidonoylglycerol release in rodent spinal cord astrocytes

Accumulating evidence supports the role of astrocytes in endocannabinoid mediated modulation of neural activity. It has been reported that some astrocytes express the cannabinoid type 1 receptor (CB(1)-R), the activation of which is leading to Ca(2+) mobilization from internal stores and a consecuti...

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Autores principales: Hegyi, Zoltán, Oláh, Tamás, Kőszeghy, Áron, Piscitelli, Fabiana, Holló, Krisztina, Pál, Balázs, Csernoch, László, Di Marzo, Vincenzo, Antal, Miklós
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043539/
https://www.ncbi.nlm.nih.gov/pubmed/30002493
http://dx.doi.org/10.1038/s41598-018-28763-6
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author Hegyi, Zoltán
Oláh, Tamás
Kőszeghy, Áron
Piscitelli, Fabiana
Holló, Krisztina
Pál, Balázs
Csernoch, László
Di Marzo, Vincenzo
Antal, Miklós
author_facet Hegyi, Zoltán
Oláh, Tamás
Kőszeghy, Áron
Piscitelli, Fabiana
Holló, Krisztina
Pál, Balázs
Csernoch, László
Di Marzo, Vincenzo
Antal, Miklós
author_sort Hegyi, Zoltán
collection PubMed
description Accumulating evidence supports the role of astrocytes in endocannabinoid mediated modulation of neural activity. It has been reported that some astrocytes express the cannabinoid type 1 receptor (CB(1)-R), the activation of which is leading to Ca(2+) mobilization from internal stores and a consecutive release of glutamate. It has also been documented that astrocytes have the potential to produce the endocannabinoid 2-arachidonoylglycerol, one of the best known CB(1)-R agonist. However, no relationship between CB(1)-R activation and 2-arachidonoylglycerol production has ever been demonstrated. Here we show that rat spinal astrocytes co-express CB(1)-Rs and the 2-arachidonoylglycerol synthesizing enzyme, diacylglycerol lipase-alpha in close vicinity to each other. We also demonstrate that activation of CB(1)-Rs induces a substantial elevation of intracellular Ca(2+) concentration in astrocytes. Finally, we provide evidence that the evoked Ca(2+) transients lead to the production of 2-arachidonoylglycerol in cultured astrocytes. The results provide evidence for a novel cannabinoid induced endocannabinoid release mechanism in astrocytes which broadens the bidirectional signaling repertoire between astrocytes and neurons.
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spelling pubmed-60435392018-07-15 CB(1) receptor activation induces intracellular Ca(2+) mobilization and 2-arachidonoylglycerol release in rodent spinal cord astrocytes Hegyi, Zoltán Oláh, Tamás Kőszeghy, Áron Piscitelli, Fabiana Holló, Krisztina Pál, Balázs Csernoch, László Di Marzo, Vincenzo Antal, Miklós Sci Rep Article Accumulating evidence supports the role of astrocytes in endocannabinoid mediated modulation of neural activity. It has been reported that some astrocytes express the cannabinoid type 1 receptor (CB(1)-R), the activation of which is leading to Ca(2+) mobilization from internal stores and a consecutive release of glutamate. It has also been documented that astrocytes have the potential to produce the endocannabinoid 2-arachidonoylglycerol, one of the best known CB(1)-R agonist. However, no relationship between CB(1)-R activation and 2-arachidonoylglycerol production has ever been demonstrated. Here we show that rat spinal astrocytes co-express CB(1)-Rs and the 2-arachidonoylglycerol synthesizing enzyme, diacylglycerol lipase-alpha in close vicinity to each other. We also demonstrate that activation of CB(1)-Rs induces a substantial elevation of intracellular Ca(2+) concentration in astrocytes. Finally, we provide evidence that the evoked Ca(2+) transients lead to the production of 2-arachidonoylglycerol in cultured astrocytes. The results provide evidence for a novel cannabinoid induced endocannabinoid release mechanism in astrocytes which broadens the bidirectional signaling repertoire between astrocytes and neurons. Nature Publishing Group UK 2018-07-12 /pmc/articles/PMC6043539/ /pubmed/30002493 http://dx.doi.org/10.1038/s41598-018-28763-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hegyi, Zoltán
Oláh, Tamás
Kőszeghy, Áron
Piscitelli, Fabiana
Holló, Krisztina
Pál, Balázs
Csernoch, László
Di Marzo, Vincenzo
Antal, Miklós
CB(1) receptor activation induces intracellular Ca(2+) mobilization and 2-arachidonoylglycerol release in rodent spinal cord astrocytes
title CB(1) receptor activation induces intracellular Ca(2+) mobilization and 2-arachidonoylglycerol release in rodent spinal cord astrocytes
title_full CB(1) receptor activation induces intracellular Ca(2+) mobilization and 2-arachidonoylglycerol release in rodent spinal cord astrocytes
title_fullStr CB(1) receptor activation induces intracellular Ca(2+) mobilization and 2-arachidonoylglycerol release in rodent spinal cord astrocytes
title_full_unstemmed CB(1) receptor activation induces intracellular Ca(2+) mobilization and 2-arachidonoylglycerol release in rodent spinal cord astrocytes
title_short CB(1) receptor activation induces intracellular Ca(2+) mobilization and 2-arachidonoylglycerol release in rodent spinal cord astrocytes
title_sort cb(1) receptor activation induces intracellular ca(2+) mobilization and 2-arachidonoylglycerol release in rodent spinal cord astrocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043539/
https://www.ncbi.nlm.nih.gov/pubmed/30002493
http://dx.doi.org/10.1038/s41598-018-28763-6
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