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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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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. |
format | Online Article Text |
id | pubmed-7908016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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