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A Dual-Labeling Probe for Super-Resolution Imaging to Detect Mitochondrial Reactive Sulfur Species in Live Cells

Background: Mitochondria are the main sites of reactive sulfur species (RSS) production in living cells. RSS in mitochondria play an important role in physiological and pathological processes of life. In this study, a dual-labeling probe that could simultaneously label the mitochondrial membrane and...

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Autores principales: Hu, Maomao, Wang, Boyang, Zhang, Hongdan, Wang, Han, Li, Huixin, Zhang, Xinyu, Zhang, Jinjin, Lu, Qianrun, Fang, Guiqian, Wang, Juan, Dong, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9198575/
https://www.ncbi.nlm.nih.gov/pubmed/35721202
http://dx.doi.org/10.3389/fphar.2022.871059
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author Hu, Maomao
Wang, Boyang
Zhang, Hongdan
Wang, Han
Li, Huixin
Zhang, Xinyu
Zhang, Jinjin
Lu, Qianrun
Fang, Guiqian
Wang, Juan
Dong, Bo
author_facet Hu, Maomao
Wang, Boyang
Zhang, Hongdan
Wang, Han
Li, Huixin
Zhang, Xinyu
Zhang, Jinjin
Lu, Qianrun
Fang, Guiqian
Wang, Juan
Dong, Bo
author_sort Hu, Maomao
collection PubMed
description Background: Mitochondria are the main sites of reactive sulfur species (RSS) production in living cells. RSS in mitochondria play an important role in physiological and pathological processes of life. In this study, a dual-labeling probe that could simultaneously label the mitochondrial membrane and matrix was designed to quantitatively detect RSS of mitochondria in living cells using nano-level super-resolution imaging. Methods: A fluorescent probe CPE was designed and synthesized. The cytotoxicity of CPE was determined and co-localization of CPE with a commercial mitochondrial probe was analyzed in HeLa cells. Then, the uptake patterns of CPE in HeLa cells at different temperatures and endocytosis levels were investigated. The staining characteristics of CPE under different conditions were imaged and quantitated under structured illumination microscopy. Results: A fluorescence probe CPE reacting to RSS was developed, which could simultaneously label the mitochondrial membrane with green fluorescence and the mitochondrial matrix with red fluorescence. CPE was able to demonstrate the mitochondrial morphology and detect the changes of RSS in mitochondria. With the increase of mitochondrial RSS concentration, the light of the red matrix will be quenched. Conclusion: CPE provides a strategy for the design of probes and an attractive tool for accurate examination to changes of mitochondrial morphology and RSS in mitochondria in living cells at the nanoscale.
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spelling pubmed-91985752022-06-16 A Dual-Labeling Probe for Super-Resolution Imaging to Detect Mitochondrial Reactive Sulfur Species in Live Cells Hu, Maomao Wang, Boyang Zhang, Hongdan Wang, Han Li, Huixin Zhang, Xinyu Zhang, Jinjin Lu, Qianrun Fang, Guiqian Wang, Juan Dong, Bo Front Pharmacol Pharmacology Background: Mitochondria are the main sites of reactive sulfur species (RSS) production in living cells. RSS in mitochondria play an important role in physiological and pathological processes of life. In this study, a dual-labeling probe that could simultaneously label the mitochondrial membrane and matrix was designed to quantitatively detect RSS of mitochondria in living cells using nano-level super-resolution imaging. Methods: A fluorescent probe CPE was designed and synthesized. The cytotoxicity of CPE was determined and co-localization of CPE with a commercial mitochondrial probe was analyzed in HeLa cells. Then, the uptake patterns of CPE in HeLa cells at different temperatures and endocytosis levels were investigated. The staining characteristics of CPE under different conditions were imaged and quantitated under structured illumination microscopy. Results: A fluorescence probe CPE reacting to RSS was developed, which could simultaneously label the mitochondrial membrane with green fluorescence and the mitochondrial matrix with red fluorescence. CPE was able to demonstrate the mitochondrial morphology and detect the changes of RSS in mitochondria. With the increase of mitochondrial RSS concentration, the light of the red matrix will be quenched. Conclusion: CPE provides a strategy for the design of probes and an attractive tool for accurate examination to changes of mitochondrial morphology and RSS in mitochondria in living cells at the nanoscale. Frontiers Media S.A. 2022-06-01 /pmc/articles/PMC9198575/ /pubmed/35721202 http://dx.doi.org/10.3389/fphar.2022.871059 Text en Copyright © 2022 Hu, Wang, Zhang, Wang, Li, Zhang, Zhang, Lu, Fang, Wang and Dong. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Hu, Maomao
Wang, Boyang
Zhang, Hongdan
Wang, Han
Li, Huixin
Zhang, Xinyu
Zhang, Jinjin
Lu, Qianrun
Fang, Guiqian
Wang, Juan
Dong, Bo
A Dual-Labeling Probe for Super-Resolution Imaging to Detect Mitochondrial Reactive Sulfur Species in Live Cells
title A Dual-Labeling Probe for Super-Resolution Imaging to Detect Mitochondrial Reactive Sulfur Species in Live Cells
title_full A Dual-Labeling Probe for Super-Resolution Imaging to Detect Mitochondrial Reactive Sulfur Species in Live Cells
title_fullStr A Dual-Labeling Probe for Super-Resolution Imaging to Detect Mitochondrial Reactive Sulfur Species in Live Cells
title_full_unstemmed A Dual-Labeling Probe for Super-Resolution Imaging to Detect Mitochondrial Reactive Sulfur Species in Live Cells
title_short A Dual-Labeling Probe for Super-Resolution Imaging to Detect Mitochondrial Reactive Sulfur Species in Live Cells
title_sort dual-labeling probe for super-resolution imaging to detect mitochondrial reactive sulfur species in live cells
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9198575/
https://www.ncbi.nlm.nih.gov/pubmed/35721202
http://dx.doi.org/10.3389/fphar.2022.871059
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