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Optogenetic Control of Apoptosis in Targeted Tissues of Xenopus laevis Embryos

KillerRed (KR) is a recently discovered fluorescent protein that, when activated with green light, releases reactive oxygen species (ROS) into the cytoplasm, triggering apoptosis in a KR-expressing cell. This property allows for the use of KR as a means of killing cells in an organism with great tem...

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Detalles Bibliográficos
Autores principales: Jewhurst, Kyle, Levin, Michael, McLaughlin, Kelly A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213186/
https://www.ncbi.nlm.nih.gov/pubmed/25374461
http://dx.doi.org/10.4137/JCD.S18368
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author Jewhurst, Kyle
Levin, Michael
McLaughlin, Kelly A
author_facet Jewhurst, Kyle
Levin, Michael
McLaughlin, Kelly A
author_sort Jewhurst, Kyle
collection PubMed
description KillerRed (KR) is a recently discovered fluorescent protein that, when activated with green light, releases reactive oxygen species (ROS) into the cytoplasm, triggering apoptosis in a KR-expressing cell. This property allows for the use of KR as a means of killing cells in an organism with great temporal and spatial specificity, while minimizing the nonspecific effects that can result from mechanical or chemical exposure damage techniques. Such optogenetic control of cell death, and the resulting ability to induce the targeted death of specific tissues, is invaluable for regeneration/repair studies—particularly in Xenopus laevis, where apoptosis plays a key role in regeneration and repair. We here describe a method by which membrane-bound KR, introduced to Xenopus embryos by mRNA microinjection, can be activated with green light to induce apoptosis in specific organs and tissues, with a focus on the developing eye and pronephric kidney.
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spelling pubmed-42131862014-11-05 Optogenetic Control of Apoptosis in Targeted Tissues of Xenopus laevis Embryos Jewhurst, Kyle Levin, Michael McLaughlin, Kelly A J Cell Death Methodology KillerRed (KR) is a recently discovered fluorescent protein that, when activated with green light, releases reactive oxygen species (ROS) into the cytoplasm, triggering apoptosis in a KR-expressing cell. This property allows for the use of KR as a means of killing cells in an organism with great temporal and spatial specificity, while minimizing the nonspecific effects that can result from mechanical or chemical exposure damage techniques. Such optogenetic control of cell death, and the resulting ability to induce the targeted death of specific tissues, is invaluable for regeneration/repair studies—particularly in Xenopus laevis, where apoptosis plays a key role in regeneration and repair. We here describe a method by which membrane-bound KR, introduced to Xenopus embryos by mRNA microinjection, can be activated with green light to induce apoptosis in specific organs and tissues, with a focus on the developing eye and pronephric kidney. Libertas Academica 2014-10-13 /pmc/articles/PMC4213186/ /pubmed/25374461 http://dx.doi.org/10.4137/JCD.S18368 Text en © 2014 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License.
spellingShingle Methodology
Jewhurst, Kyle
Levin, Michael
McLaughlin, Kelly A
Optogenetic Control of Apoptosis in Targeted Tissues of Xenopus laevis Embryos
title Optogenetic Control of Apoptosis in Targeted Tissues of Xenopus laevis Embryos
title_full Optogenetic Control of Apoptosis in Targeted Tissues of Xenopus laevis Embryos
title_fullStr Optogenetic Control of Apoptosis in Targeted Tissues of Xenopus laevis Embryos
title_full_unstemmed Optogenetic Control of Apoptosis in Targeted Tissues of Xenopus laevis Embryos
title_short Optogenetic Control of Apoptosis in Targeted Tissues of Xenopus laevis Embryos
title_sort optogenetic control of apoptosis in targeted tissues of xenopus laevis embryos
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213186/
https://www.ncbi.nlm.nih.gov/pubmed/25374461
http://dx.doi.org/10.4137/JCD.S18368
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