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Immunohistological Localization of Mel1a Melatonin Receptor in Pigeon Retina

BACKGROUND: Melatonin (N-acetyl-5-methoxytryptamine), a significant indoleamine neuromodulator implicated in circadian rhythms and sleep patterns, regulates diverse rhythmic functions via activating its high-affinity G-protein-coupled receptors. However, the detailed cellular expression of the Mel1a...

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Autores principales: Sheng, Wenlong, Weng, Shijun, Li, Fei, Zhang, Yun, He, Qiuxia, Sheng, Wenxiang, Fu, Ying, Yan, Haiyue, Liu, Kechun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7872906/
https://www.ncbi.nlm.nih.gov/pubmed/33574722
http://dx.doi.org/10.2147/NSS.S290757
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author Sheng, Wenlong
Weng, Shijun
Li, Fei
Zhang, Yun
He, Qiuxia
Sheng, Wenxiang
Fu, Ying
Yan, Haiyue
Liu, Kechun
author_facet Sheng, Wenlong
Weng, Shijun
Li, Fei
Zhang, Yun
He, Qiuxia
Sheng, Wenxiang
Fu, Ying
Yan, Haiyue
Liu, Kechun
author_sort Sheng, Wenlong
collection PubMed
description BACKGROUND: Melatonin (N-acetyl-5-methoxytryptamine), a significant indoleamine neuromodulator implicated in circadian rhythms and sleep patterns, regulates diverse rhythmic functions via activating its high-affinity G-protein-coupled receptors. However, the detailed cellular expression of the Mel1a receptor in the retina is still a research gap. METHODS: The expression of the Mel1a receptor in pigeon retina was assessed using Western blot analysis and immunofluorescent staining. The cellular localization of the Mel1a receptor was studied using double immunofluorescent staining and laser-scanning confocal microscopy. RESULTS: Our data suggested that the Mel1a receptor was extensively expressed in the outer segment of Rho4D2-labeled rod and L/M-opsin-labeled red/green cone and in the somata of the CB-labeled horizontal cell, TH-labeled dopaminergic amacrine cell, ChAT-labeled cholinergic amacrine cell, PV-labeled AII amacrine cell, Brn3a-labeled conventional ganglion cell, melanopsin-containing ganglion cell and CRALBP-labeled Müller glial cell. In addition, the Mel1a receptor was diffusely distributed throughout the full thickness of the inner plexiform layer. However, the outer segment of S-opsin-labeled blue cone, the somata of ChX-10-labeled bipolar cell and outer plexiform layer seemed to lack immunoreactivity of the Mel1a receptor. CONCLUSION: The finding that multiple types of retinal cells express the Mel1a receptor provides a new neurobiological basis for the participation of melatonin in the regulation of retinal functions through activating the Mel1a receptor.
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spelling pubmed-78729062021-02-10 Immunohistological Localization of Mel1a Melatonin Receptor in Pigeon Retina Sheng, Wenlong Weng, Shijun Li, Fei Zhang, Yun He, Qiuxia Sheng, Wenxiang Fu, Ying Yan, Haiyue Liu, Kechun Nat Sci Sleep Original Research BACKGROUND: Melatonin (N-acetyl-5-methoxytryptamine), a significant indoleamine neuromodulator implicated in circadian rhythms and sleep patterns, regulates diverse rhythmic functions via activating its high-affinity G-protein-coupled receptors. However, the detailed cellular expression of the Mel1a receptor in the retina is still a research gap. METHODS: The expression of the Mel1a receptor in pigeon retina was assessed using Western blot analysis and immunofluorescent staining. The cellular localization of the Mel1a receptor was studied using double immunofluorescent staining and laser-scanning confocal microscopy. RESULTS: Our data suggested that the Mel1a receptor was extensively expressed in the outer segment of Rho4D2-labeled rod and L/M-opsin-labeled red/green cone and in the somata of the CB-labeled horizontal cell, TH-labeled dopaminergic amacrine cell, ChAT-labeled cholinergic amacrine cell, PV-labeled AII amacrine cell, Brn3a-labeled conventional ganglion cell, melanopsin-containing ganglion cell and CRALBP-labeled Müller glial cell. In addition, the Mel1a receptor was diffusely distributed throughout the full thickness of the inner plexiform layer. However, the outer segment of S-opsin-labeled blue cone, the somata of ChX-10-labeled bipolar cell and outer plexiform layer seemed to lack immunoreactivity of the Mel1a receptor. CONCLUSION: The finding that multiple types of retinal cells express the Mel1a receptor provides a new neurobiological basis for the participation of melatonin in the regulation of retinal functions through activating the Mel1a receptor. Dove 2021-02-05 /pmc/articles/PMC7872906/ /pubmed/33574722 http://dx.doi.org/10.2147/NSS.S290757 Text en © 2021 Sheng et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Sheng, Wenlong
Weng, Shijun
Li, Fei
Zhang, Yun
He, Qiuxia
Sheng, Wenxiang
Fu, Ying
Yan, Haiyue
Liu, Kechun
Immunohistological Localization of Mel1a Melatonin Receptor in Pigeon Retina
title Immunohistological Localization of Mel1a Melatonin Receptor in Pigeon Retina
title_full Immunohistological Localization of Mel1a Melatonin Receptor in Pigeon Retina
title_fullStr Immunohistological Localization of Mel1a Melatonin Receptor in Pigeon Retina
title_full_unstemmed Immunohistological Localization of Mel1a Melatonin Receptor in Pigeon Retina
title_short Immunohistological Localization of Mel1a Melatonin Receptor in Pigeon Retina
title_sort immunohistological localization of mel1a melatonin receptor in pigeon retina
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7872906/
https://www.ncbi.nlm.nih.gov/pubmed/33574722
http://dx.doi.org/10.2147/NSS.S290757
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