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Monitoring of relative mitochondrial membrane potential in living cells by fluorescence microscopy

Permeant cationic fluorescent probes are shown to be selectively accumulated by the mitochondria of living cells. Mitochondria-specific interaction of such molecules is apparently dependent on the high trans- membrane potential (inside negative) maintained by functional mitochondria. Dissipation of...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1981
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112765/
https://www.ncbi.nlm.nih.gov/pubmed/6783667
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description Permeant cationic fluorescent probes are shown to be selectively accumulated by the mitochondria of living cells. Mitochondria-specific interaction of such molecules is apparently dependent on the high trans- membrane potential (inside negative) maintained by functional mitochondria. Dissipation of the mitochondrial trans-membrane and potential by ionophores or inhibitors of electron transport eliminates the selective mitochondrial association of these compounds. The application of such potential-dependent probes in conjunction with fluorescence microscopy allows the monitoring of mitochondrial membrane potential in individual living cells. Marked elevations in mitochondria- associated probe fluorescence have been observed in cells engaged in active movement. This approach to the analysis of mitochondrial membrane potential should be of value in future investigations of the control of energy metabolism and energy requirements of specific biological functions at the cellular level.
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spelling pubmed-21127652008-05-01 Monitoring of relative mitochondrial membrane potential in living cells by fluorescence microscopy J Cell Biol Articles Permeant cationic fluorescent probes are shown to be selectively accumulated by the mitochondria of living cells. Mitochondria-specific interaction of such molecules is apparently dependent on the high trans- membrane potential (inside negative) maintained by functional mitochondria. Dissipation of the mitochondrial trans-membrane and potential by ionophores or inhibitors of electron transport eliminates the selective mitochondrial association of these compounds. The application of such potential-dependent probes in conjunction with fluorescence microscopy allows the monitoring of mitochondrial membrane potential in individual living cells. Marked elevations in mitochondria- associated probe fluorescence have been observed in cells engaged in active movement. This approach to the analysis of mitochondrial membrane potential should be of value in future investigations of the control of energy metabolism and energy requirements of specific biological functions at the cellular level. The Rockefeller University Press 1981-03-01 /pmc/articles/PMC2112765/ /pubmed/6783667 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Monitoring of relative mitochondrial membrane potential in living cells by fluorescence microscopy
title Monitoring of relative mitochondrial membrane potential in living cells by fluorescence microscopy
title_full Monitoring of relative mitochondrial membrane potential in living cells by fluorescence microscopy
title_fullStr Monitoring of relative mitochondrial membrane potential in living cells by fluorescence microscopy
title_full_unstemmed Monitoring of relative mitochondrial membrane potential in living cells by fluorescence microscopy
title_short Monitoring of relative mitochondrial membrane potential in living cells by fluorescence microscopy
title_sort monitoring of relative mitochondrial membrane potential in living cells by fluorescence microscopy
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112765/
https://www.ncbi.nlm.nih.gov/pubmed/6783667