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Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor
Distinct spatiotemporal Ca(2+) signalling events regulate fundamental aspects of eukaryotic cell physiology. Complex Ca(2+) signals can be driven by release of Ca(2+) from intracellular organelles that sequester Ca(2+) such as the ER (endoplasmic reticulum) or through the opening of Ca(2+)-permeable...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526116/ https://www.ncbi.nlm.nih.gov/pubmed/23098255 http://dx.doi.org/10.1042/BJ20120898 |
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author | McCue, Hannah V. Wardyn, Joanna D. Burgoyne, Robert D. Haynes, Lee P. |
author_facet | McCue, Hannah V. Wardyn, Joanna D. Burgoyne, Robert D. Haynes, Lee P. |
author_sort | McCue, Hannah V. |
collection | PubMed |
description | Distinct spatiotemporal Ca(2+) signalling events regulate fundamental aspects of eukaryotic cell physiology. Complex Ca(2+) signals can be driven by release of Ca(2+) from intracellular organelles that sequester Ca(2+) such as the ER (endoplasmic reticulum) or through the opening of Ca(2+)-permeable channels in the plasma membrane and influx of extracellular Ca(2+). Late endocytic pathway compartments including late-endosomes and lysosomes have recently been observed to sequester Ca(2+) to levels comparable with those found within the ER lumen. These organelles harbour ligand-gated Ca(2+)-release channels and evidence indicates that they can operate as Ca(2+)-signalling platforms. Lysosomes sequester Ca(2+) to a greater extent than any other endocytic compartment, and signalling from this organelle has been postulated to provide ‘trigger’ release events that can subsequently elicit more extensive Ca(2+) signals from stores including the ER. In order to investigate lysosomal-specific Ca(2+) signalling a simple method for measuring lysosomal Ca(2+) release is essential. In the present study we describe the generation and characterization of a genetically encoded, lysosomally targeted, cameleon sensor which is capable of registering specific Ca(2+) release in response to extracellular agonists and intracellular second messengers. This probe represents a novel tool that will permit detailed investigations examining the impact of lysosomal Ca(2+) handling on cellular physiology. |
format | Online Article Text |
id | pubmed-3526116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35261162012-12-19 Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor McCue, Hannah V. Wardyn, Joanna D. Burgoyne, Robert D. Haynes, Lee P. Biochem J Research Article Distinct spatiotemporal Ca(2+) signalling events regulate fundamental aspects of eukaryotic cell physiology. Complex Ca(2+) signals can be driven by release of Ca(2+) from intracellular organelles that sequester Ca(2+) such as the ER (endoplasmic reticulum) or through the opening of Ca(2+)-permeable channels in the plasma membrane and influx of extracellular Ca(2+). Late endocytic pathway compartments including late-endosomes and lysosomes have recently been observed to sequester Ca(2+) to levels comparable with those found within the ER lumen. These organelles harbour ligand-gated Ca(2+)-release channels and evidence indicates that they can operate as Ca(2+)-signalling platforms. Lysosomes sequester Ca(2+) to a greater extent than any other endocytic compartment, and signalling from this organelle has been postulated to provide ‘trigger’ release events that can subsequently elicit more extensive Ca(2+) signals from stores including the ER. In order to investigate lysosomal-specific Ca(2+) signalling a simple method for measuring lysosomal Ca(2+) release is essential. In the present study we describe the generation and characterization of a genetically encoded, lysosomally targeted, cameleon sensor which is capable of registering specific Ca(2+) release in response to extracellular agonists and intracellular second messengers. This probe represents a novel tool that will permit detailed investigations examining the impact of lysosomal Ca(2+) handling on cellular physiology. Portland Press Ltd. 2012-12-14 2013-01-15 /pmc/articles/PMC3526116/ /pubmed/23098255 http://dx.doi.org/10.1042/BJ20120898 Text en © 2013 The Author(s) The author(s) has paid for this article to be freely available under the terms of the Creative Commons Attribution Non-Commercial Licence (http://creativecommons.org/licenses/by-nc/2.5/) which permits unrestricted non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by-nc/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article McCue, Hannah V. Wardyn, Joanna D. Burgoyne, Robert D. Haynes, Lee P. Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor |
title | Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor |
title_full | Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor |
title_fullStr | Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor |
title_full_unstemmed | Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor |
title_short | Generation and characterization of a lysosomally targeted, genetically encoded Ca(2+)-sensor |
title_sort | generation and characterization of a lysosomally targeted, genetically encoded ca(2+)-sensor |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526116/ https://www.ncbi.nlm.nih.gov/pubmed/23098255 http://dx.doi.org/10.1042/BJ20120898 |
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