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Quantitatively Monitoring In Situ Mitochondrial Thermal Dynamics by Upconversion Nanoparticles

[Image: see text] Temperature dynamics reflect the physiological conditions of cells and organisms. Mitochondria regulate the temperature dynamics in living cells as they oxidize the respiratory substrates and synthesize ATP, with heat being released as a byproduct of active metabolism. Here, we rep...

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Autores principales: Di, Xiangjun, Wang, Dejiang, Zhou, Jiajia, Zhang, Lin, Stenzel, Martina H., Su, Qian Peter, Jin, Dayong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908016/
https://www.ncbi.nlm.nih.gov/pubmed/33550807
http://dx.doi.org/10.1021/acs.nanolett.0c04281
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author Di, Xiangjun
Wang, Dejiang
Zhou, Jiajia
Zhang, Lin
Stenzel, Martina H.
Su, Qian Peter
Jin, Dayong
author_facet Di, Xiangjun
Wang, Dejiang
Zhou, Jiajia
Zhang, Lin
Stenzel, Martina H.
Su, Qian Peter
Jin, Dayong
author_sort Di, Xiangjun
collection PubMed
description [Image: see text] Temperature dynamics reflect the physiological conditions of cells and organisms. Mitochondria regulate the temperature dynamics in living cells as they oxidize the respiratory substrates and synthesize ATP, with heat being released as a byproduct of active metabolism. Here, we report an upconversion nanoparticle-based thermometer that allows the in situ thermal dynamics monitoring of mitochondria in living cells. We demonstrate that the upconversion nanothermometers can efficiently target mitochondria, and the temperature-responsive feature is independent of probe concentration and medium conditions. The relative sensing sensitivity of 3.2% K(–1) in HeLa cells allows us to measure the mitochondrial temperature difference through the stimulations of high glucose, lipid, Ca(2+) shock, and the inhibitor of oxidative phosphorylation. Moreover, cells display distinct response time and thermodynamic profiles under different stimulations, which highlight the potential applications of this thermometer to study in situ vital processes related to mitochondrial metabolism pathways and interactions between organelles.
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spelling pubmed-79080162021-02-26 Quantitatively Monitoring In Situ Mitochondrial Thermal Dynamics by Upconversion Nanoparticles Di, Xiangjun Wang, Dejiang Zhou, Jiajia Zhang, Lin Stenzel, Martina H. Su, Qian Peter Jin, Dayong Nano Lett [Image: see text] Temperature dynamics reflect the physiological conditions of cells and organisms. Mitochondria regulate the temperature dynamics in living cells as they oxidize the respiratory substrates and synthesize ATP, with heat being released as a byproduct of active metabolism. Here, we report an upconversion nanoparticle-based thermometer that allows the in situ thermal dynamics monitoring of mitochondria in living cells. We demonstrate that the upconversion nanothermometers can efficiently target mitochondria, and the temperature-responsive feature is independent of probe concentration and medium conditions. The relative sensing sensitivity of 3.2% K(–1) in HeLa cells allows us to measure the mitochondrial temperature difference through the stimulations of high glucose, lipid, Ca(2+) shock, and the inhibitor of oxidative phosphorylation. Moreover, cells display distinct response time and thermodynamic profiles under different stimulations, which highlight the potential applications of this thermometer to study in situ vital processes related to mitochondrial metabolism pathways and interactions between organelles. American Chemical Society 2021-02-06 2021-02-24 /pmc/articles/PMC7908016/ /pubmed/33550807 http://dx.doi.org/10.1021/acs.nanolett.0c04281 Text en © 2021 American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Di, Xiangjun
Wang, Dejiang
Zhou, Jiajia
Zhang, Lin
Stenzel, Martina H.
Su, Qian Peter
Jin, Dayong
Quantitatively Monitoring In Situ Mitochondrial Thermal Dynamics by Upconversion Nanoparticles
title Quantitatively Monitoring In Situ Mitochondrial Thermal Dynamics by Upconversion Nanoparticles
title_full Quantitatively Monitoring In Situ Mitochondrial Thermal Dynamics by Upconversion Nanoparticles
title_fullStr Quantitatively Monitoring In Situ Mitochondrial Thermal Dynamics by Upconversion Nanoparticles
title_full_unstemmed Quantitatively Monitoring In Situ Mitochondrial Thermal Dynamics by Upconversion Nanoparticles
title_short Quantitatively Monitoring In Situ Mitochondrial Thermal Dynamics by Upconversion Nanoparticles
title_sort quantitatively monitoring in situ mitochondrial thermal dynamics by upconversion nanoparticles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908016/
https://www.ncbi.nlm.nih.gov/pubmed/33550807
http://dx.doi.org/10.1021/acs.nanolett.0c04281
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