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A new fluorescent sensor mitoferrofluor indicates the presence of chelatable iron in polarized and depolarized mitochondria

Mitochondrial chelatable iron contributes to the severity of several injury processes, including ischemia/reperfusion, oxidative stress, and drug toxicity. However, methods to measure this species in living cells are lacking. To measure mitochondrial chelatable iron in living cells, here we synthesi...

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Autores principales: Kholmukhamedov, Andaleb, Li, Li, Lindsey, Christopher C., Hu, Jiangting, Nieminen, Anna-Liisa, Takemoto, Kenji, Beeson, Gyda C., Beneker, Chad M., McInnes, Campbell, Beeson, Craig C., Lemasters, John J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9460511/
https://www.ncbi.nlm.nih.gov/pubmed/35931111
http://dx.doi.org/10.1016/j.jbc.2022.102336
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author Kholmukhamedov, Andaleb
Li, Li
Lindsey, Christopher C.
Hu, Jiangting
Nieminen, Anna-Liisa
Takemoto, Kenji
Beeson, Gyda C.
Beneker, Chad M.
McInnes, Campbell
Beeson, Craig C.
Lemasters, John J.
author_facet Kholmukhamedov, Andaleb
Li, Li
Lindsey, Christopher C.
Hu, Jiangting
Nieminen, Anna-Liisa
Takemoto, Kenji
Beeson, Gyda C.
Beneker, Chad M.
McInnes, Campbell
Beeson, Craig C.
Lemasters, John J.
author_sort Kholmukhamedov, Andaleb
collection PubMed
description Mitochondrial chelatable iron contributes to the severity of several injury processes, including ischemia/reperfusion, oxidative stress, and drug toxicity. However, methods to measure this species in living cells are lacking. To measure mitochondrial chelatable iron in living cells, here we synthesized a new fluorescent indicator, mitoferrofluor (MFF). We designed cationic MFF to accumulate electrophoretically in polarized mitochondria, where a reactive group then forms covalent adducts with mitochondrial proteins to retain MFF even after subsequent depolarization. We also show in cell-free medium that Fe(2+) (and Cu(2+)), but not Fe(3+), Ca(2+), or other biologically relevant divalent cations, strongly quenched MFF fluorescence. Using confocal microscopy, we demonstrate in hepatocytes that red MFF fluorescence colocalized with the green fluorescence of the mitochondrial membrane potential (ΔΨ(m)) indicator, rhodamine 123 (Rh123), indicating selective accumulation into the mitochondria. Unlike Rh123, mitochondria retained MFF after ΔΨ(m) collapse. Furthermore, intracellular delivery of iron with membrane-permeant Fe(3+)/8-hydroxyquinoline (FeHQ) quenched MFF fluorescence by ∼80% in hepatocytes and other cell lines, which was substantially restored by the membrane-permeant transition metal chelator pyridoxal isonicotinoyl hydrazone. We also show FeHQ quenched the fluorescence of cytosolically coloaded calcein, another Fe(2+) indicator, confirming that Fe(3+) in FeHQ undergoes intracellular reduction to Fe(2+). Finally, MFF fluorescence did not change after addition of the calcium mobilizer thapsigargin, which shows MFF is insensitive to physiologically relevant increases of mitochondrial Ca(2+). In conclusion, the new sensor reagent MFF fluorescence is an indicator of mitochondrial chelatable Fe(2+) in normal hepatocytes with polarized mitochondria as well as in cells undergoing loss of ΔΨ(m).
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spelling pubmed-94605112022-09-12 A new fluorescent sensor mitoferrofluor indicates the presence of chelatable iron in polarized and depolarized mitochondria Kholmukhamedov, Andaleb Li, Li Lindsey, Christopher C. Hu, Jiangting Nieminen, Anna-Liisa Takemoto, Kenji Beeson, Gyda C. Beneker, Chad M. McInnes, Campbell Beeson, Craig C. Lemasters, John J. J Biol Chem Research Article Mitochondrial chelatable iron contributes to the severity of several injury processes, including ischemia/reperfusion, oxidative stress, and drug toxicity. However, methods to measure this species in living cells are lacking. To measure mitochondrial chelatable iron in living cells, here we synthesized a new fluorescent indicator, mitoferrofluor (MFF). We designed cationic MFF to accumulate electrophoretically in polarized mitochondria, where a reactive group then forms covalent adducts with mitochondrial proteins to retain MFF even after subsequent depolarization. We also show in cell-free medium that Fe(2+) (and Cu(2+)), but not Fe(3+), Ca(2+), or other biologically relevant divalent cations, strongly quenched MFF fluorescence. Using confocal microscopy, we demonstrate in hepatocytes that red MFF fluorescence colocalized with the green fluorescence of the mitochondrial membrane potential (ΔΨ(m)) indicator, rhodamine 123 (Rh123), indicating selective accumulation into the mitochondria. Unlike Rh123, mitochondria retained MFF after ΔΨ(m) collapse. Furthermore, intracellular delivery of iron with membrane-permeant Fe(3+)/8-hydroxyquinoline (FeHQ) quenched MFF fluorescence by ∼80% in hepatocytes and other cell lines, which was substantially restored by the membrane-permeant transition metal chelator pyridoxal isonicotinoyl hydrazone. We also show FeHQ quenched the fluorescence of cytosolically coloaded calcein, another Fe(2+) indicator, confirming that Fe(3+) in FeHQ undergoes intracellular reduction to Fe(2+). Finally, MFF fluorescence did not change after addition of the calcium mobilizer thapsigargin, which shows MFF is insensitive to physiologically relevant increases of mitochondrial Ca(2+). In conclusion, the new sensor reagent MFF fluorescence is an indicator of mitochondrial chelatable Fe(2+) in normal hepatocytes with polarized mitochondria as well as in cells undergoing loss of ΔΨ(m). American Society for Biochemistry and Molecular Biology 2022-08-02 /pmc/articles/PMC9460511/ /pubmed/35931111 http://dx.doi.org/10.1016/j.jbc.2022.102336 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Kholmukhamedov, Andaleb
Li, Li
Lindsey, Christopher C.
Hu, Jiangting
Nieminen, Anna-Liisa
Takemoto, Kenji
Beeson, Gyda C.
Beneker, Chad M.
McInnes, Campbell
Beeson, Craig C.
Lemasters, John J.
A new fluorescent sensor mitoferrofluor indicates the presence of chelatable iron in polarized and depolarized mitochondria
title A new fluorescent sensor mitoferrofluor indicates the presence of chelatable iron in polarized and depolarized mitochondria
title_full A new fluorescent sensor mitoferrofluor indicates the presence of chelatable iron in polarized and depolarized mitochondria
title_fullStr A new fluorescent sensor mitoferrofluor indicates the presence of chelatable iron in polarized and depolarized mitochondria
title_full_unstemmed A new fluorescent sensor mitoferrofluor indicates the presence of chelatable iron in polarized and depolarized mitochondria
title_short A new fluorescent sensor mitoferrofluor indicates the presence of chelatable iron in polarized and depolarized mitochondria
title_sort new fluorescent sensor mitoferrofluor indicates the presence of chelatable iron in polarized and depolarized mitochondria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9460511/
https://www.ncbi.nlm.nih.gov/pubmed/35931111
http://dx.doi.org/10.1016/j.jbc.2022.102336
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