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The discovery, structure, and function of 5-HTR1E serotonin receptor

Serotonin (5-hydroxytryptamine, 5-HT) is a unique neurotransmitter which can regulate various biological processes by activating thirteen different receptors. These serotonin receptors are divided into seven different classes based on their structure and functions. Since these receptors co-express i...

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Autores principales: Sharma, Vinay Kumar, Loh, Y. Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506339/
https://www.ncbi.nlm.nih.gov/pubmed/37723479
http://dx.doi.org/10.1186/s12964-023-01195-0
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author Sharma, Vinay Kumar
Loh, Y. Peng
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Loh, Y. Peng
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description Serotonin (5-hydroxytryptamine, 5-HT) is a unique neurotransmitter which can regulate various biological processes by activating thirteen different receptors. These serotonin receptors are divided into seven different classes based on their structure and functions. Since these receptors co-express in various tissue and cell types and share the same ligand (5-HT), it has been a challenge for the researchers to define specific pathway and separate physiological role for each of these serotonin receptors. Though the evidence of operational diversity of these receptors is continuously emerging, much work remains to be done. 5-HTR1E is a member of 5-HT1 receptor family which belongs to G-protein coupled receptors (GPCRs). Even after three decades since its discovery, 5-HTR1E remains the least explored serotonin receptor. Very high similarity with another family member (5-HTR1F) and its non-existence in mice or rats makes 5-HTR1E a difficult target to study. Despite these challenges, recent findings on the role of 5-HTR1E in neuroprotection and diseases such as cancer, have excited many researchers to explore this receptor in detail. Here, we provide the first review of 5-HTR1E, since its discovery in 1989 to 2023. We highlight the structural and functional characteristics of this important serotonin receptor in detail and propose future directions in developing 5-HTR1E as a drug target. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-023-01195-0.
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spelling pubmed-105063392023-09-19 The discovery, structure, and function of 5-HTR1E serotonin receptor Sharma, Vinay Kumar Loh, Y. Peng Cell Commun Signal Review Serotonin (5-hydroxytryptamine, 5-HT) is a unique neurotransmitter which can regulate various biological processes by activating thirteen different receptors. These serotonin receptors are divided into seven different classes based on their structure and functions. Since these receptors co-express in various tissue and cell types and share the same ligand (5-HT), it has been a challenge for the researchers to define specific pathway and separate physiological role for each of these serotonin receptors. Though the evidence of operational diversity of these receptors is continuously emerging, much work remains to be done. 5-HTR1E is a member of 5-HT1 receptor family which belongs to G-protein coupled receptors (GPCRs). Even after three decades since its discovery, 5-HTR1E remains the least explored serotonin receptor. Very high similarity with another family member (5-HTR1F) and its non-existence in mice or rats makes 5-HTR1E a difficult target to study. Despite these challenges, recent findings on the role of 5-HTR1E in neuroprotection and diseases such as cancer, have excited many researchers to explore this receptor in detail. Here, we provide the first review of 5-HTR1E, since its discovery in 1989 to 2023. We highlight the structural and functional characteristics of this important serotonin receptor in detail and propose future directions in developing 5-HTR1E as a drug target. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-023-01195-0. BioMed Central 2023-09-18 /pmc/articles/PMC10506339/ /pubmed/37723479 http://dx.doi.org/10.1186/s12964-023-01195-0 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Sharma, Vinay Kumar
Loh, Y. Peng
The discovery, structure, and function of 5-HTR1E serotonin receptor
title The discovery, structure, and function of 5-HTR1E serotonin receptor
title_full The discovery, structure, and function of 5-HTR1E serotonin receptor
title_fullStr The discovery, structure, and function of 5-HTR1E serotonin receptor
title_full_unstemmed The discovery, structure, and function of 5-HTR1E serotonin receptor
title_short The discovery, structure, and function of 5-HTR1E serotonin receptor
title_sort discovery, structure, and function of 5-htr1e serotonin receptor
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506339/
https://www.ncbi.nlm.nih.gov/pubmed/37723479
http://dx.doi.org/10.1186/s12964-023-01195-0
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