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Development of Chemical Tools for Imaging of Fe(II) Ions in Living Cells: A Review

Intracellular labile iron is an iron species which is not or weakly bound to proteins and depicts an important effect on homeostatic regulation in cells. An excess or deficiency of iron can cause oxidative damage to key cellular biomolecules. The behavior and concentrations of labile iron are diffic...

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Detalles Bibliográficos
Autor principal: Hirayama, Tasuku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6261839/
https://www.ncbi.nlm.nih.gov/pubmed/30510327
http://dx.doi.org/10.1267/ahc.18015
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author Hirayama, Tasuku
author_facet Hirayama, Tasuku
author_sort Hirayama, Tasuku
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description Intracellular labile iron is an iron species which is not or weakly bound to proteins and depicts an important effect on homeostatic regulation in cells. An excess or deficiency of iron can cause oxidative damage to key cellular biomolecules. The behavior and concentrations of labile iron are difficult to monitor, but the specific redox state of the Fe ions is relevant to the physiological and pathological properties that we would like to study. We have developed a series of turn-on type fluorescent probes that are highly selective to the labile Fe(II) ions, and we have tested their applications to cellular level imaging. These probes are based on N-oxide chemistry with a range of fluorophores that depict optimal performance for specific applications. Herein, I review the recent progress of our research and discuss prospects for future work to understand the relation between intracellular ion and oxidative stress.
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spelling pubmed-62618392018-12-03 Development of Chemical Tools for Imaging of Fe(II) Ions in Living Cells: A Review Hirayama, Tasuku Acta Histochem Cytochem Review Intracellular labile iron is an iron species which is not or weakly bound to proteins and depicts an important effect on homeostatic regulation in cells. An excess or deficiency of iron can cause oxidative damage to key cellular biomolecules. The behavior and concentrations of labile iron are difficult to monitor, but the specific redox state of the Fe ions is relevant to the physiological and pathological properties that we would like to study. We have developed a series of turn-on type fluorescent probes that are highly selective to the labile Fe(II) ions, and we have tested their applications to cellular level imaging. These probes are based on N-oxide chemistry with a range of fluorophores that depict optimal performance for specific applications. Herein, I review the recent progress of our research and discuss prospects for future work to understand the relation between intracellular ion and oxidative stress. JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY 2018-10-31 2018-10-30 /pmc/articles/PMC6261839/ /pubmed/30510327 http://dx.doi.org/10.1267/ahc.18015 Text en 2018 The Japan Society of Histochemistry and Cytochemistry This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Hirayama, Tasuku
Development of Chemical Tools for Imaging of Fe(II) Ions in Living Cells: A Review
title Development of Chemical Tools for Imaging of Fe(II) Ions in Living Cells: A Review
title_full Development of Chemical Tools for Imaging of Fe(II) Ions in Living Cells: A Review
title_fullStr Development of Chemical Tools for Imaging of Fe(II) Ions in Living Cells: A Review
title_full_unstemmed Development of Chemical Tools for Imaging of Fe(II) Ions in Living Cells: A Review
title_short Development of Chemical Tools for Imaging of Fe(II) Ions in Living Cells: A Review
title_sort development of chemical tools for imaging of fe(ii) ions in living cells: a review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6261839/
https://www.ncbi.nlm.nih.gov/pubmed/30510327
http://dx.doi.org/10.1267/ahc.18015
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