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Evidence for a functional adrenomedullin signaling pathway in the mouse retina
PURPOSE: Adrenomedullin (ADM) is a small, secreted peptide often associated with vasodilation. However, ADM can also function as a neurotransmitter/neuromodulator, and studies suggest ADM is upregulated in the eye in several ocular diseases. However, no studies to date have described an ADM signalin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3369892/ https://www.ncbi.nlm.nih.gov/pubmed/22690112 |
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author | Blom, Jan Giove, Thomas J. Pong, Winnie W. Blute, Todd A. Eldred, William D. |
author_facet | Blom, Jan Giove, Thomas J. Pong, Winnie W. Blute, Todd A. Eldred, William D. |
author_sort | Blom, Jan |
collection | PubMed |
description | PURPOSE: Adrenomedullin (ADM) is a small, secreted peptide often associated with vasodilation. However, ADM can also function as a neurotransmitter/neuromodulator, and studies suggest ADM is upregulated in the eye in several ocular diseases. However, no studies to date have described an ADM signaling pathway in the retina. METHODS: PCR, immunocytochemistry, nitric oxide imaging, western blots, and a nitrite assay were used to determine the localization of the components of the ADM signaling pathway in the mouse retina. RESULTS: We used reverse-transcriptase polymerase chain reaction to show that ADM and its primary receptor, calcitonin-receptor-like receptor, along with its associated receptor activity modifying proteins 2 and 3 are expressed in the retina. Using immunocytochemistry, we detected ADM staining throughout the retina in the photoreceptor outer segments, the outer nuclear layer, Müller and amacrine cell somata in the inner nuclear layer, and some somata in the ganglion cell layer. We found that calcitonin-receptor-like receptor and receptor activity modifying protein 2 had localization patterns similar to ADM, especially in somata in the inner nuclear and ganglion cell layers. Finally, we showed that the ADM receptor was functional in the retina. Stimulation of isolated retinas with ADM increased cyclic adenosine monophosphate– and cyclic guanosine monophosphate–like immunoreactivity, as well as nitric oxide production. CONCLUSIONS: These results are the first to show that ADM and functional ADM receptors are present in the retina. Since ADM is increased in eyes with ocular pathologies such as diabetic retinopathy, glaucoma, retinitis pigmentosa, and uveitis, the ADM signaling pathway may provide a new target for ameliorating these retinal pathologies. |
format | Online Article Text |
id | pubmed-3369892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Molecular Vision |
record_format | MEDLINE/PubMed |
spelling | pubmed-33698922012-06-11 Evidence for a functional adrenomedullin signaling pathway in the mouse retina Blom, Jan Giove, Thomas J. Pong, Winnie W. Blute, Todd A. Eldred, William D. Mol Vis Research Article PURPOSE: Adrenomedullin (ADM) is a small, secreted peptide often associated with vasodilation. However, ADM can also function as a neurotransmitter/neuromodulator, and studies suggest ADM is upregulated in the eye in several ocular diseases. However, no studies to date have described an ADM signaling pathway in the retina. METHODS: PCR, immunocytochemistry, nitric oxide imaging, western blots, and a nitrite assay were used to determine the localization of the components of the ADM signaling pathway in the mouse retina. RESULTS: We used reverse-transcriptase polymerase chain reaction to show that ADM and its primary receptor, calcitonin-receptor-like receptor, along with its associated receptor activity modifying proteins 2 and 3 are expressed in the retina. Using immunocytochemistry, we detected ADM staining throughout the retina in the photoreceptor outer segments, the outer nuclear layer, Müller and amacrine cell somata in the inner nuclear layer, and some somata in the ganglion cell layer. We found that calcitonin-receptor-like receptor and receptor activity modifying protein 2 had localization patterns similar to ADM, especially in somata in the inner nuclear and ganglion cell layers. Finally, we showed that the ADM receptor was functional in the retina. Stimulation of isolated retinas with ADM increased cyclic adenosine monophosphate– and cyclic guanosine monophosphate–like immunoreactivity, as well as nitric oxide production. CONCLUSIONS: These results are the first to show that ADM and functional ADM receptors are present in the retina. Since ADM is increased in eyes with ocular pathologies such as diabetic retinopathy, glaucoma, retinitis pigmentosa, and uveitis, the ADM signaling pathway may provide a new target for ameliorating these retinal pathologies. Molecular Vision 2012-05-30 /pmc/articles/PMC3369892/ /pubmed/22690112 Text en Copyright © 2012 Molecular Vision. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Blom, Jan Giove, Thomas J. Pong, Winnie W. Blute, Todd A. Eldred, William D. Evidence for a functional adrenomedullin signaling pathway in the mouse retina |
title | Evidence for a functional adrenomedullin signaling pathway in the mouse retina |
title_full | Evidence for a functional adrenomedullin signaling pathway in the mouse retina |
title_fullStr | Evidence for a functional adrenomedullin signaling pathway in the mouse retina |
title_full_unstemmed | Evidence for a functional adrenomedullin signaling pathway in the mouse retina |
title_short | Evidence for a functional adrenomedullin signaling pathway in the mouse retina |
title_sort | evidence for a functional adrenomedullin signaling pathway in the mouse retina |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3369892/ https://www.ncbi.nlm.nih.gov/pubmed/22690112 |
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