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Mitochondrial Membranes of Human SH-SY5Y Neuroblastoma Cells Express Serotonin 5-HT(7) Receptor

Mitochondria in neurons contribute to energy supply, the regulation of synaptic transmission, Ca(2+) homeostasis, neuronal excitability, and stress adaptation. In recent years, several studies have highlighted that the neurotransmitter serotonin (5-HT) plays an important role in mitochondrial biogen...

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Autores principales: Tempio, Alessandra, Niso, Mauro, Laera, Luna, Trisolini, Lucia, Favia, Maria, Ciranna, Lucia, Marzulli, Domenico, Petrosillo, Giuseppe, Pierri, Ciro Leonardo, Lacivita, Enza, Leopoldo, Marcello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766962/
https://www.ncbi.nlm.nih.gov/pubmed/33348850
http://dx.doi.org/10.3390/ijms21249629
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author Tempio, Alessandra
Niso, Mauro
Laera, Luna
Trisolini, Lucia
Favia, Maria
Ciranna, Lucia
Marzulli, Domenico
Petrosillo, Giuseppe
Pierri, Ciro Leonardo
Lacivita, Enza
Leopoldo, Marcello
author_facet Tempio, Alessandra
Niso, Mauro
Laera, Luna
Trisolini, Lucia
Favia, Maria
Ciranna, Lucia
Marzulli, Domenico
Petrosillo, Giuseppe
Pierri, Ciro Leonardo
Lacivita, Enza
Leopoldo, Marcello
author_sort Tempio, Alessandra
collection PubMed
description Mitochondria in neurons contribute to energy supply, the regulation of synaptic transmission, Ca(2+) homeostasis, neuronal excitability, and stress adaptation. In recent years, several studies have highlighted that the neurotransmitter serotonin (5-HT) plays an important role in mitochondrial biogenesis in cortical neurons, and regulates mitochondrial activity and cellular function in cardiomyocytes. 5-HT exerts its diverse actions by binding to cell surface receptors that are classified into seven distinct families (5-HT1 to 5-HT7). Recently, it was shown that 5-HT3 and 5-HT4 receptors are located on the mitochondrial membrane and participate in the regulation of mitochondrial function. Furthermore, it was observed that activation of brain 5-HT7 receptors rescued mitochondrial dysfunction in female mice from two models of Rett syndrome, a rare neurodevelopmental disorder characterized by severe behavioral and physiological symptoms. Our Western blot analyses performed on cell-lysate and purified mitochondria isolated from neuronal cell line SH-SY5Y showed that 5-HT7 receptors are also expressed into mitochondria. Maximal binding capacity (Bmax) obtained by Scatchard analysis on purified mitochondrial membranes was 0.081 pmol/mg of 5-HT7 receptor protein. Lastly, we evaluated the effect of selective 5-HT7 receptor agonist LP-211 and antagonist (inverse agonist) SB-269970 on mitochondrial respiratory chain (MRC) cytochrome c oxidase activity on mitochondria from SH-SY5Y cells. Our findings provide the first evidence that 5-HT7 receptor is also expressed in mitochondria.
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spelling pubmed-77669622020-12-28 Mitochondrial Membranes of Human SH-SY5Y Neuroblastoma Cells Express Serotonin 5-HT(7) Receptor Tempio, Alessandra Niso, Mauro Laera, Luna Trisolini, Lucia Favia, Maria Ciranna, Lucia Marzulli, Domenico Petrosillo, Giuseppe Pierri, Ciro Leonardo Lacivita, Enza Leopoldo, Marcello Int J Mol Sci Communication Mitochondria in neurons contribute to energy supply, the regulation of synaptic transmission, Ca(2+) homeostasis, neuronal excitability, and stress adaptation. In recent years, several studies have highlighted that the neurotransmitter serotonin (5-HT) plays an important role in mitochondrial biogenesis in cortical neurons, and regulates mitochondrial activity and cellular function in cardiomyocytes. 5-HT exerts its diverse actions by binding to cell surface receptors that are classified into seven distinct families (5-HT1 to 5-HT7). Recently, it was shown that 5-HT3 and 5-HT4 receptors are located on the mitochondrial membrane and participate in the regulation of mitochondrial function. Furthermore, it was observed that activation of brain 5-HT7 receptors rescued mitochondrial dysfunction in female mice from two models of Rett syndrome, a rare neurodevelopmental disorder characterized by severe behavioral and physiological symptoms. Our Western blot analyses performed on cell-lysate and purified mitochondria isolated from neuronal cell line SH-SY5Y showed that 5-HT7 receptors are also expressed into mitochondria. Maximal binding capacity (Bmax) obtained by Scatchard analysis on purified mitochondrial membranes was 0.081 pmol/mg of 5-HT7 receptor protein. Lastly, we evaluated the effect of selective 5-HT7 receptor agonist LP-211 and antagonist (inverse agonist) SB-269970 on mitochondrial respiratory chain (MRC) cytochrome c oxidase activity on mitochondria from SH-SY5Y cells. Our findings provide the first evidence that 5-HT7 receptor is also expressed in mitochondria. MDPI 2020-12-17 /pmc/articles/PMC7766962/ /pubmed/33348850 http://dx.doi.org/10.3390/ijms21249629 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Tempio, Alessandra
Niso, Mauro
Laera, Luna
Trisolini, Lucia
Favia, Maria
Ciranna, Lucia
Marzulli, Domenico
Petrosillo, Giuseppe
Pierri, Ciro Leonardo
Lacivita, Enza
Leopoldo, Marcello
Mitochondrial Membranes of Human SH-SY5Y Neuroblastoma Cells Express Serotonin 5-HT(7) Receptor
title Mitochondrial Membranes of Human SH-SY5Y Neuroblastoma Cells Express Serotonin 5-HT(7) Receptor
title_full Mitochondrial Membranes of Human SH-SY5Y Neuroblastoma Cells Express Serotonin 5-HT(7) Receptor
title_fullStr Mitochondrial Membranes of Human SH-SY5Y Neuroblastoma Cells Express Serotonin 5-HT(7) Receptor
title_full_unstemmed Mitochondrial Membranes of Human SH-SY5Y Neuroblastoma Cells Express Serotonin 5-HT(7) Receptor
title_short Mitochondrial Membranes of Human SH-SY5Y Neuroblastoma Cells Express Serotonin 5-HT(7) Receptor
title_sort mitochondrial membranes of human sh-sy5y neuroblastoma cells express serotonin 5-ht(7) receptor
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766962/
https://www.ncbi.nlm.nih.gov/pubmed/33348850
http://dx.doi.org/10.3390/ijms21249629
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