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A high content, small molecule screen identifies candidate molecular pathways that regulate rod photoreceptor outer segment renewal
The outer segment of the vertebrate rod photoreceptor is a highly modified cilium composed of many discrete membranous discs that are filled with the protein machinery necessary for phototransduction. The unique outer segment structure is renewed daily with growth at the base of the outer segment wh...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143611/ https://www.ncbi.nlm.nih.gov/pubmed/30228302 http://dx.doi.org/10.1038/s41598-018-32336-y |
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author | Campbell, Leah J. West, Megan C. Jensen, Abbie M. |
author_facet | Campbell, Leah J. West, Megan C. Jensen, Abbie M. |
author_sort | Campbell, Leah J. |
collection | PubMed |
description | The outer segment of the vertebrate rod photoreceptor is a highly modified cilium composed of many discrete membranous discs that are filled with the protein machinery necessary for phototransduction. The unique outer segment structure is renewed daily with growth at the base of the outer segment where new discs are formed and shedding at the distal end where old discs are phagocytized by the retinal pigment epithelium. In order to understand how outer segment renewal is regulated to maintain outer segment length and function, we used a small molecule screening approach with the transgenic (hsp70:HA-mCherry(TM)) zebrafish, which expresses a genetically-encoded marker of outer segment renewal. We identified compounds with known bioactivity that affect five content areas: outer segment growth, outer segment shedding, clearance of shed outer segment tips, Rhodopsin mislocalization, and differentiation at the ciliary marginal zone. Signaling pathways that are targeted by the identified compounds include cyclooxygenase in outer segment growth, γ-Secretase in outer segment shedding, and mTor in RPE phagocytosis. The data generated by this screen provides a foundation for further investigation of the signaling pathways that regulate photoreceptor outer segment renewal. |
format | Online Article Text |
id | pubmed-6143611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61436112018-09-24 A high content, small molecule screen identifies candidate molecular pathways that regulate rod photoreceptor outer segment renewal Campbell, Leah J. West, Megan C. Jensen, Abbie M. Sci Rep Article The outer segment of the vertebrate rod photoreceptor is a highly modified cilium composed of many discrete membranous discs that are filled with the protein machinery necessary for phototransduction. The unique outer segment structure is renewed daily with growth at the base of the outer segment where new discs are formed and shedding at the distal end where old discs are phagocytized by the retinal pigment epithelium. In order to understand how outer segment renewal is regulated to maintain outer segment length and function, we used a small molecule screening approach with the transgenic (hsp70:HA-mCherry(TM)) zebrafish, which expresses a genetically-encoded marker of outer segment renewal. We identified compounds with known bioactivity that affect five content areas: outer segment growth, outer segment shedding, clearance of shed outer segment tips, Rhodopsin mislocalization, and differentiation at the ciliary marginal zone. Signaling pathways that are targeted by the identified compounds include cyclooxygenase in outer segment growth, γ-Secretase in outer segment shedding, and mTor in RPE phagocytosis. The data generated by this screen provides a foundation for further investigation of the signaling pathways that regulate photoreceptor outer segment renewal. Nature Publishing Group UK 2018-09-18 /pmc/articles/PMC6143611/ /pubmed/30228302 http://dx.doi.org/10.1038/s41598-018-32336-y 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 Campbell, Leah J. West, Megan C. Jensen, Abbie M. A high content, small molecule screen identifies candidate molecular pathways that regulate rod photoreceptor outer segment renewal |
title | A high content, small molecule screen identifies candidate molecular pathways that regulate rod photoreceptor outer segment renewal |
title_full | A high content, small molecule screen identifies candidate molecular pathways that regulate rod photoreceptor outer segment renewal |
title_fullStr | A high content, small molecule screen identifies candidate molecular pathways that regulate rod photoreceptor outer segment renewal |
title_full_unstemmed | A high content, small molecule screen identifies candidate molecular pathways that regulate rod photoreceptor outer segment renewal |
title_short | A high content, small molecule screen identifies candidate molecular pathways that regulate rod photoreceptor outer segment renewal |
title_sort | high content, small molecule screen identifies candidate molecular pathways that regulate rod photoreceptor outer segment renewal |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143611/ https://www.ncbi.nlm.nih.gov/pubmed/30228302 http://dx.doi.org/10.1038/s41598-018-32336-y |
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