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Sub-nanomolar sensitive GZnP3 reveals TRPML1-mediated neuronal Zn(2+) signals
Although numerous fluorescent Zn(2+) sensors have been reported, it is unclear whether and how Zn(2+) can be released from the intracellular compartments into the cytosol due to a lack of probes that can detect physiological dynamics of cytosolic Zn(2+). Here, we create a genetically encoded sensor,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805855/ https://www.ncbi.nlm.nih.gov/pubmed/31641116 http://dx.doi.org/10.1038/s41467-019-12761-x |
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author | Minckley, Taylor F. Zhang, Chen Fudge, Dylan H. Dischler, Anna M. LeJeune, Kate D. Xu, Haoxing Qin, Yan |
author_facet | Minckley, Taylor F. Zhang, Chen Fudge, Dylan H. Dischler, Anna M. LeJeune, Kate D. Xu, Haoxing Qin, Yan |
author_sort | Minckley, Taylor F. |
collection | PubMed |
description | Although numerous fluorescent Zn(2+) sensors have been reported, it is unclear whether and how Zn(2+) can be released from the intracellular compartments into the cytosol due to a lack of probes that can detect physiological dynamics of cytosolic Zn(2+). Here, we create a genetically encoded sensor, GZnP3, which demonstrates unprecedented sensitivity for Zn(2+) at sub-nanomolar concentrations. Using GZnP3 as well as GZnP3-derived vesicular targeted probes, we provide the first direct evidence that Zn(2+) can be released from endolysosomal vesicles to the cytosol in primary hippocampal neurons through the TRPML1 channel. Such TRPML1-mediated Zn(2+) signals are distinct from Ca(2+) in that they are selectively present in neurons, sustain longer, and are significantly higher in neurites as compared to the soma. Together, our work not only creates highly sensitive probes for investigating sub-nanomolar Zn(2+) dynamics, but also reveals new pools of Zn(2+) signals that can play critical roles in neuronal function. |
format | Online Article Text |
id | pubmed-6805855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68058552019-10-24 Sub-nanomolar sensitive GZnP3 reveals TRPML1-mediated neuronal Zn(2+) signals Minckley, Taylor F. Zhang, Chen Fudge, Dylan H. Dischler, Anna M. LeJeune, Kate D. Xu, Haoxing Qin, Yan Nat Commun Article Although numerous fluorescent Zn(2+) sensors have been reported, it is unclear whether and how Zn(2+) can be released from the intracellular compartments into the cytosol due to a lack of probes that can detect physiological dynamics of cytosolic Zn(2+). Here, we create a genetically encoded sensor, GZnP3, which demonstrates unprecedented sensitivity for Zn(2+) at sub-nanomolar concentrations. Using GZnP3 as well as GZnP3-derived vesicular targeted probes, we provide the first direct evidence that Zn(2+) can be released from endolysosomal vesicles to the cytosol in primary hippocampal neurons through the TRPML1 channel. Such TRPML1-mediated Zn(2+) signals are distinct from Ca(2+) in that they are selectively present in neurons, sustain longer, and are significantly higher in neurites as compared to the soma. Together, our work not only creates highly sensitive probes for investigating sub-nanomolar Zn(2+) dynamics, but also reveals new pools of Zn(2+) signals that can play critical roles in neuronal function. Nature Publishing Group UK 2019-10-22 /pmc/articles/PMC6805855/ /pubmed/31641116 http://dx.doi.org/10.1038/s41467-019-12761-x Text en © The Author(s) 2019 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 Minckley, Taylor F. Zhang, Chen Fudge, Dylan H. Dischler, Anna M. LeJeune, Kate D. Xu, Haoxing Qin, Yan Sub-nanomolar sensitive GZnP3 reveals TRPML1-mediated neuronal Zn(2+) signals |
title | Sub-nanomolar sensitive GZnP3 reveals TRPML1-mediated neuronal Zn(2+) signals |
title_full | Sub-nanomolar sensitive GZnP3 reveals TRPML1-mediated neuronal Zn(2+) signals |
title_fullStr | Sub-nanomolar sensitive GZnP3 reveals TRPML1-mediated neuronal Zn(2+) signals |
title_full_unstemmed | Sub-nanomolar sensitive GZnP3 reveals TRPML1-mediated neuronal Zn(2+) signals |
title_short | Sub-nanomolar sensitive GZnP3 reveals TRPML1-mediated neuronal Zn(2+) signals |
title_sort | sub-nanomolar sensitive gznp3 reveals trpml1-mediated neuronal zn(2+) signals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805855/ https://www.ncbi.nlm.nih.gov/pubmed/31641116 http://dx.doi.org/10.1038/s41467-019-12761-x |
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