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All-optical spatiotemporal mapping of ROS dynamics across mitochondrial microdomains in situ
Hydrogen peroxide (H(2)O(2)) functions as a second messenger to signal metabolic distress through highly compartmentalized production in mitochondria. The dynamics of reactive oxygen species (ROS) generation and diffusion between mitochondrial compartments and into the cytosol govern oxidative stres...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533892/ https://www.ncbi.nlm.nih.gov/pubmed/37758713 http://dx.doi.org/10.1038/s41467-023-41682-z |
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author | Koren, Shon A. Ahmed Selim, Nada De la Rosa, Lizbeth Horn, Jacob Farooqi, M. Arsalan Wei, Alicia Y. Müller-Eigner, Annika Emerson, Jacen Johnson, Gail V. W. Wojtovich, Andrew P. |
author_facet | Koren, Shon A. Ahmed Selim, Nada De la Rosa, Lizbeth Horn, Jacob Farooqi, M. Arsalan Wei, Alicia Y. Müller-Eigner, Annika Emerson, Jacen Johnson, Gail V. W. Wojtovich, Andrew P. |
author_sort | Koren, Shon A. |
collection | PubMed |
description | Hydrogen peroxide (H(2)O(2)) functions as a second messenger to signal metabolic distress through highly compartmentalized production in mitochondria. The dynamics of reactive oxygen species (ROS) generation and diffusion between mitochondrial compartments and into the cytosol govern oxidative stress responses and pathology, though these processes remain poorly understood. Here, we couple the H(2)O(2) biosensor, HyPer7, with optogenetic stimulation of the ROS-generating protein KillerRed targeted into multiple mitochondrial microdomains. Single mitochondrial photogeneration of H(2)O(2) demonstrates the spatiotemporal dynamics of ROS diffusion and transient hyperfusion of mitochondria due to ROS. This transient hyperfusion phenotype required mitochondrial fusion but not fission machinery. Measurement of microdomain-specific H(2)O(2) diffusion kinetics reveals directionally selective diffusion through mitochondrial microdomains. All-optical generation and detection of physiologically-relevant concentrations of H(2)O(2) between mitochondrial compartments provide a map of mitochondrial H(2)O(2) diffusion dynamics in situ as a framework to understand the role of ROS in health and disease. |
format | Online Article Text |
id | pubmed-10533892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105338922023-09-29 All-optical spatiotemporal mapping of ROS dynamics across mitochondrial microdomains in situ Koren, Shon A. Ahmed Selim, Nada De la Rosa, Lizbeth Horn, Jacob Farooqi, M. Arsalan Wei, Alicia Y. Müller-Eigner, Annika Emerson, Jacen Johnson, Gail V. W. Wojtovich, Andrew P. Nat Commun Article Hydrogen peroxide (H(2)O(2)) functions as a second messenger to signal metabolic distress through highly compartmentalized production in mitochondria. The dynamics of reactive oxygen species (ROS) generation and diffusion between mitochondrial compartments and into the cytosol govern oxidative stress responses and pathology, though these processes remain poorly understood. Here, we couple the H(2)O(2) biosensor, HyPer7, with optogenetic stimulation of the ROS-generating protein KillerRed targeted into multiple mitochondrial microdomains. Single mitochondrial photogeneration of H(2)O(2) demonstrates the spatiotemporal dynamics of ROS diffusion and transient hyperfusion of mitochondria due to ROS. This transient hyperfusion phenotype required mitochondrial fusion but not fission machinery. Measurement of microdomain-specific H(2)O(2) diffusion kinetics reveals directionally selective diffusion through mitochondrial microdomains. All-optical generation and detection of physiologically-relevant concentrations of H(2)O(2) between mitochondrial compartments provide a map of mitochondrial H(2)O(2) diffusion dynamics in situ as a framework to understand the role of ROS in health and disease. Nature Publishing Group UK 2023-09-27 /pmc/articles/PMC10533892/ /pubmed/37758713 http://dx.doi.org/10.1038/s41467-023-41682-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Koren, Shon A. Ahmed Selim, Nada De la Rosa, Lizbeth Horn, Jacob Farooqi, M. Arsalan Wei, Alicia Y. Müller-Eigner, Annika Emerson, Jacen Johnson, Gail V. W. Wojtovich, Andrew P. All-optical spatiotemporal mapping of ROS dynamics across mitochondrial microdomains in situ |
title | All-optical spatiotemporal mapping of ROS dynamics across mitochondrial microdomains in situ |
title_full | All-optical spatiotemporal mapping of ROS dynamics across mitochondrial microdomains in situ |
title_fullStr | All-optical spatiotemporal mapping of ROS dynamics across mitochondrial microdomains in situ |
title_full_unstemmed | All-optical spatiotemporal mapping of ROS dynamics across mitochondrial microdomains in situ |
title_short | All-optical spatiotemporal mapping of ROS dynamics across mitochondrial microdomains in situ |
title_sort | all-optical spatiotemporal mapping of ros dynamics across mitochondrial microdomains in situ |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533892/ https://www.ncbi.nlm.nih.gov/pubmed/37758713 http://dx.doi.org/10.1038/s41467-023-41682-z |
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