Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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
_version_ 1785112273240457216
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
work_keys_str_mv AT korenshona allopticalspatiotemporalmappingofrosdynamicsacrossmitochondrialmicrodomainsinsitu
AT ahmedselimnada allopticalspatiotemporalmappingofrosdynamicsacrossmitochondrialmicrodomainsinsitu
AT delarosalizbeth allopticalspatiotemporalmappingofrosdynamicsacrossmitochondrialmicrodomainsinsitu
AT hornjacob allopticalspatiotemporalmappingofrosdynamicsacrossmitochondrialmicrodomainsinsitu
AT farooqimarsalan allopticalspatiotemporalmappingofrosdynamicsacrossmitochondrialmicrodomainsinsitu
AT weialiciay allopticalspatiotemporalmappingofrosdynamicsacrossmitochondrialmicrodomainsinsitu
AT mullereignerannika allopticalspatiotemporalmappingofrosdynamicsacrossmitochondrialmicrodomainsinsitu
AT emersonjacen allopticalspatiotemporalmappingofrosdynamicsacrossmitochondrialmicrodomainsinsitu
AT johnsongailvw allopticalspatiotemporalmappingofrosdynamicsacrossmitochondrialmicrodomainsinsitu
AT wojtovichandrewp allopticalspatiotemporalmappingofrosdynamicsacrossmitochondrialmicrodomainsinsitu