Cargando…
Blue light excited retinal intercepts cellular signaling
Photoreceptor chromophore, 11-cis retinal (11CR) and the photoproduct, all-trans retinal (ATR), are present in the retina at higher concentrations and interact with the visual cells. Non-visual cells in the body are also exposed to retinal that enters the circulation. Although the cornea and the len...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033873/ https://www.ncbi.nlm.nih.gov/pubmed/29976989 http://dx.doi.org/10.1038/s41598-018-28254-8 |
_version_ | 1783337759184781312 |
---|---|
author | Ratnayake, Kasun Payton, John L. Lakmal, O. Harshana Karunarathne, Ajith |
author_facet | Ratnayake, Kasun Payton, John L. Lakmal, O. Harshana Karunarathne, Ajith |
author_sort | Ratnayake, Kasun |
collection | PubMed |
description | Photoreceptor chromophore, 11-cis retinal (11CR) and the photoproduct, all-trans retinal (ATR), are present in the retina at higher concentrations and interact with the visual cells. Non-visual cells in the body are also exposed to retinal that enters the circulation. Although the cornea and the lens of the eye are transparent to the blue light region where retinal can absorb and undergo excitation, the reported phototoxicity in the eye has been assigned to lipophilic non-degradable materials known as lipofuscins, which also includes retinal condensation products. The possibility of blue light excited retinal interacting with cells; intercepting signaling in the presence or absence of light has not been explored. Using live cell imaging and optogenetic signaling control, we uncovered that blue light-excited ATR and 11CR irreversibly change/distort plasma membrane (PM) bound phospholipid; phosphatidylinositol 4,5 bisphosphate (PIP2) and disrupt its function. This distortion in PIP2 was independent of visual or non-visual G-protein coupled receptor activation. The change in PIP2 was followed by an increase in the cytosolic calcium, excessive cell shape change, and cell death. Blue light alone or retinal alone did not perturb PIP2 or elicit cytosolic calcium increase. Our data also suggest that photoexcited retinal-induced PIP2 distortion and subsequent oxidative damage incur in the core of the PM. These findings suggest that retinal exerts light sensitivity to both photoreceptor and non-photoreceptor cells, and intercepts crucial signaling events, altering the cellular fate. |
format | Online Article Text |
id | pubmed-6033873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60338732018-07-12 Blue light excited retinal intercepts cellular signaling Ratnayake, Kasun Payton, John L. Lakmal, O. Harshana Karunarathne, Ajith Sci Rep Article Photoreceptor chromophore, 11-cis retinal (11CR) and the photoproduct, all-trans retinal (ATR), are present in the retina at higher concentrations and interact with the visual cells. Non-visual cells in the body are also exposed to retinal that enters the circulation. Although the cornea and the lens of the eye are transparent to the blue light region where retinal can absorb and undergo excitation, the reported phototoxicity in the eye has been assigned to lipophilic non-degradable materials known as lipofuscins, which also includes retinal condensation products. The possibility of blue light excited retinal interacting with cells; intercepting signaling in the presence or absence of light has not been explored. Using live cell imaging and optogenetic signaling control, we uncovered that blue light-excited ATR and 11CR irreversibly change/distort plasma membrane (PM) bound phospholipid; phosphatidylinositol 4,5 bisphosphate (PIP2) and disrupt its function. This distortion in PIP2 was independent of visual or non-visual G-protein coupled receptor activation. The change in PIP2 was followed by an increase in the cytosolic calcium, excessive cell shape change, and cell death. Blue light alone or retinal alone did not perturb PIP2 or elicit cytosolic calcium increase. Our data also suggest that photoexcited retinal-induced PIP2 distortion and subsequent oxidative damage incur in the core of the PM. These findings suggest that retinal exerts light sensitivity to both photoreceptor and non-photoreceptor cells, and intercepts crucial signaling events, altering the cellular fate. Nature Publishing Group UK 2018-07-05 /pmc/articles/PMC6033873/ /pubmed/29976989 http://dx.doi.org/10.1038/s41598-018-28254-8 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 Ratnayake, Kasun Payton, John L. Lakmal, O. Harshana Karunarathne, Ajith Blue light excited retinal intercepts cellular signaling |
title | Blue light excited retinal intercepts cellular signaling |
title_full | Blue light excited retinal intercepts cellular signaling |
title_fullStr | Blue light excited retinal intercepts cellular signaling |
title_full_unstemmed | Blue light excited retinal intercepts cellular signaling |
title_short | Blue light excited retinal intercepts cellular signaling |
title_sort | blue light excited retinal intercepts cellular signaling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033873/ https://www.ncbi.nlm.nih.gov/pubmed/29976989 http://dx.doi.org/10.1038/s41598-018-28254-8 |
work_keys_str_mv | AT ratnayakekasun bluelightexcitedretinalinterceptscellularsignaling AT paytonjohnl bluelightexcitedretinalinterceptscellularsignaling AT lakmaloharshana bluelightexcitedretinalinterceptscellularsignaling AT karunarathneajith bluelightexcitedretinalinterceptscellularsignaling |