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A Low Affinity GCaMP3 Variant (GCaMPer) for Imaging the Endoplasmic Reticulum Calcium Store
Endoplasmic reticulum calcium homeostasis is critical for cellular functions and is disrupted in diverse pathologies including neurodegeneration and cardiovascular disease. Owing to the high concentration of calcium within the ER, studying this subcellular compartment requires tools that are optimiz...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4599735/ https://www.ncbi.nlm.nih.gov/pubmed/26451944 http://dx.doi.org/10.1371/journal.pone.0139273 |
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author | Henderson, Mark J. Baldwin, Heather A. Werley, Christopher A. Boccardo, Stefano Whitaker, Leslie R. Yan, Xiaokang Holt, Graham T. Schreiter, Eric R. Looger, Loren L. Cohen, Adam E. Kim, Douglas S. Harvey, Brandon K. |
author_facet | Henderson, Mark J. Baldwin, Heather A. Werley, Christopher A. Boccardo, Stefano Whitaker, Leslie R. Yan, Xiaokang Holt, Graham T. Schreiter, Eric R. Looger, Loren L. Cohen, Adam E. Kim, Douglas S. Harvey, Brandon K. |
author_sort | Henderson, Mark J. |
collection | PubMed |
description | Endoplasmic reticulum calcium homeostasis is critical for cellular functions and is disrupted in diverse pathologies including neurodegeneration and cardiovascular disease. Owing to the high concentration of calcium within the ER, studying this subcellular compartment requires tools that are optimized for these conditions. To develop a single-fluorophore genetically encoded calcium indicator for this organelle, we targeted a low affinity variant of GCaMP3 to the ER lumen (GCaMPer (10.19)). A set of viral vectors was constructed to express GCaMPer in human neuroblastoma cells, rat primary cortical neurons, and human induced pluripotent stem cell-derived cardiomyocytes. We observed dynamic changes in GCaMPer (10.19) fluorescence in response to pharmacologic manipulations of the ER calcium store. Additionally, periodic calcium efflux from the ER was observed during spontaneous beating of cardiomyocytes. GCaMPer (10.19) has utility in imaging ER calcium in living cells and providing insight into luminal calcium dynamics under physiologic and pathologic states. |
format | Online Article Text |
id | pubmed-4599735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45997352015-10-20 A Low Affinity GCaMP3 Variant (GCaMPer) for Imaging the Endoplasmic Reticulum Calcium Store Henderson, Mark J. Baldwin, Heather A. Werley, Christopher A. Boccardo, Stefano Whitaker, Leslie R. Yan, Xiaokang Holt, Graham T. Schreiter, Eric R. Looger, Loren L. Cohen, Adam E. Kim, Douglas S. Harvey, Brandon K. PLoS One Research Article Endoplasmic reticulum calcium homeostasis is critical for cellular functions and is disrupted in diverse pathologies including neurodegeneration and cardiovascular disease. Owing to the high concentration of calcium within the ER, studying this subcellular compartment requires tools that are optimized for these conditions. To develop a single-fluorophore genetically encoded calcium indicator for this organelle, we targeted a low affinity variant of GCaMP3 to the ER lumen (GCaMPer (10.19)). A set of viral vectors was constructed to express GCaMPer in human neuroblastoma cells, rat primary cortical neurons, and human induced pluripotent stem cell-derived cardiomyocytes. We observed dynamic changes in GCaMPer (10.19) fluorescence in response to pharmacologic manipulations of the ER calcium store. Additionally, periodic calcium efflux from the ER was observed during spontaneous beating of cardiomyocytes. GCaMPer (10.19) has utility in imaging ER calcium in living cells and providing insight into luminal calcium dynamics under physiologic and pathologic states. Public Library of Science 2015-10-09 /pmc/articles/PMC4599735/ /pubmed/26451944 http://dx.doi.org/10.1371/journal.pone.0139273 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Henderson, Mark J. Baldwin, Heather A. Werley, Christopher A. Boccardo, Stefano Whitaker, Leslie R. Yan, Xiaokang Holt, Graham T. Schreiter, Eric R. Looger, Loren L. Cohen, Adam E. Kim, Douglas S. Harvey, Brandon K. A Low Affinity GCaMP3 Variant (GCaMPer) for Imaging the Endoplasmic Reticulum Calcium Store |
title | A Low Affinity GCaMP3 Variant (GCaMPer) for Imaging the Endoplasmic Reticulum Calcium Store |
title_full | A Low Affinity GCaMP3 Variant (GCaMPer) for Imaging the Endoplasmic Reticulum Calcium Store |
title_fullStr | A Low Affinity GCaMP3 Variant (GCaMPer) for Imaging the Endoplasmic Reticulum Calcium Store |
title_full_unstemmed | A Low Affinity GCaMP3 Variant (GCaMPer) for Imaging the Endoplasmic Reticulum Calcium Store |
title_short | A Low Affinity GCaMP3 Variant (GCaMPer) for Imaging the Endoplasmic Reticulum Calcium Store |
title_sort | low affinity gcamp3 variant (gcamper) for imaging the endoplasmic reticulum calcium store |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4599735/ https://www.ncbi.nlm.nih.gov/pubmed/26451944 http://dx.doi.org/10.1371/journal.pone.0139273 |
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