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  1. 原著論文

Radiation-induced long-lived extracellular radicals do not contribute to measurement of intracellular reactive oxygen species using the dichlorofluorescein method

https://repo.qst.go.jp/records/45137
https://repo.qst.go.jp/records/45137
1bdf658c-0d8f-479d-bff9-a24583352c82
Item type 学術雑誌論文 / Journal Article(1)
公開日 2008-04-17
タイトル
タイトル Radiation-induced long-lived extracellular radicals do not contribute to measurement of intracellular reactive oxygen species using the dichlorofluorescein method
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Hafer, Kurt

× Hafer, Kurt

WEKO 448212

Hafer, Kurt

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Konishi, Teruaki

× Konishi, Teruaki

WEKO 448213

Konishi, Teruaki

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Robert, Schiestl

× Robert, Schiestl

WEKO 448214

Robert, Schiestl

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Hafer Kurt

× Hafer Kurt

WEKO 448215

en Hafer Kurt

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小西 輝昭

× 小西 輝昭

WEKO 448216

en 小西 輝昭

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Robert Schiestl

× Robert Schiestl

WEKO 448217

en Robert Schiestl

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内容記述タイプ Abstract
内容記述 The dichlorofluorescein method has become a standard technique for measuring reactive oxygen species (ROS) formed in cells by ionizing radiation. A recent report [Y.N. Korystov, V.V. Shaposhnikova, A.F. Korystova, M.O. Emel'yanov, Detection of Reactive Oxygen Species Induced by Radiation in Cells Using the Dichlorofluorescein Assay. Radiat. Res. (2007)] has suggested the method is subject to an artifact in which it erroneously reports hydrogen peroxides generated in the extracellular medium as ROS formed intracellularly by ionizing radiation. It was hypothesized that such ionizing radiation-induced extracellular peroxides influx into cells in the minutes following radiation exposure and subsequently oxidize the intracellular dichlorofluorescin probe and that dichlorofluorescein fluorescence is not due to ROS formed by ionizing radiation intracellularly. Here we test this hypothesis by measuring the contribution of long-lived radicals formed in medium by ionizing radiation on intracellular dichlorofluorescein fluorescence. We find no evidence that such an artifact significantly contributes to intracellular dichlorofluorescein fluorescence. These results and those of Y.N. Korystov et al. are discussed in view of cellular dichlorofluorescin leakage and radiation chemistry. We conclude that the dichlorofluorescein method remains effective for quantifying intracellular ROS induced by ionizing radiation.
書誌情報 Radiation Research

巻 169, 号 4, p. 469-473, 発行日 2008-04
ISSN
収録物識別子タイプ ISSN
収録物識別子 0033-7587
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