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Hepcidin-2 in mouse urine as a candidate radiation-responsive molecule

We used high-performance liquid chromatography to separate urine obtained from whole-body gamma-irradiated mice (4 Gy) before analyzing each fraction with matrix-assisted laser desorption/ionization–time-of-flight mass spectrometry to identify radiation-responsive molecules. We identified two candid...

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Autores principales: Iizuka, Daisuke, Yoshioka, Susumu, Kawai, Hidehiko, Okazaki, Emi, Kiriyama, Keita, Izumi, Shunsuke, Nishimura, Mayumi, Shimada, Yoshiya, Kamiya, Kenji, Suzuki, Fumio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795955/
https://www.ncbi.nlm.nih.gov/pubmed/26826199
http://dx.doi.org/10.1093/jrr/rrv098
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author Iizuka, Daisuke
Yoshioka, Susumu
Kawai, Hidehiko
Okazaki, Emi
Kiriyama, Keita
Izumi, Shunsuke
Nishimura, Mayumi
Shimada, Yoshiya
Kamiya, Kenji
Suzuki, Fumio
author_facet Iizuka, Daisuke
Yoshioka, Susumu
Kawai, Hidehiko
Okazaki, Emi
Kiriyama, Keita
Izumi, Shunsuke
Nishimura, Mayumi
Shimada, Yoshiya
Kamiya, Kenji
Suzuki, Fumio
author_sort Iizuka, Daisuke
collection PubMed
description We used high-performance liquid chromatography to separate urine obtained from whole-body gamma-irradiated mice (4 Gy) before analyzing each fraction with matrix-assisted laser desorption/ionization–time-of-flight mass spectrometry to identify radiation-responsive molecules. We identified two candidates: hepcidin antimicrobial peptide 2 (hepcidin-2) and peptide fragments of kidney androgen-regulated protein (KAP). We observed that peak increases of hepcidin-2 in urine were delayed in a dose-dependent manner (1 Gy and above); however, the amount of KAP peptide fragments showed no correlation with radiation dose. In addition, an increase in hepcidin-2 after exposure to relatively low radiation doses (0.25 and 0.5 Gy, respectively) was biphasic (at 8–48 h and 120–168 h, respectively, after irradiation). The increase in hepcidin-2 paralleled an increase in hepcidin-2 gene ( Hamp2 ) mRNA levels in the liver. These results suggest that radiation exposure directly or indirectly induces urinary excretion of hepcidin-2 at least in part by the upregulation of Hamp2 mRNA in the liver.
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spelling pubmed-47959552016-03-21 Hepcidin-2 in mouse urine as a candidate radiation-responsive molecule Iizuka, Daisuke Yoshioka, Susumu Kawai, Hidehiko Okazaki, Emi Kiriyama, Keita Izumi, Shunsuke Nishimura, Mayumi Shimada, Yoshiya Kamiya, Kenji Suzuki, Fumio J Radiat Res Biology We used high-performance liquid chromatography to separate urine obtained from whole-body gamma-irradiated mice (4 Gy) before analyzing each fraction with matrix-assisted laser desorption/ionization–time-of-flight mass spectrometry to identify radiation-responsive molecules. We identified two candidates: hepcidin antimicrobial peptide 2 (hepcidin-2) and peptide fragments of kidney androgen-regulated protein (KAP). We observed that peak increases of hepcidin-2 in urine were delayed in a dose-dependent manner (1 Gy and above); however, the amount of KAP peptide fragments showed no correlation with radiation dose. In addition, an increase in hepcidin-2 after exposure to relatively low radiation doses (0.25 and 0.5 Gy, respectively) was biphasic (at 8–48 h and 120–168 h, respectively, after irradiation). The increase in hepcidin-2 paralleled an increase in hepcidin-2 gene ( Hamp2 ) mRNA levels in the liver. These results suggest that radiation exposure directly or indirectly induces urinary excretion of hepcidin-2 at least in part by the upregulation of Hamp2 mRNA in the liver. Oxford University Press 2016-03 2016-01-28 /pmc/articles/PMC4795955/ /pubmed/26826199 http://dx.doi.org/10.1093/jrr/rrv098 Text en © The Author 2016. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Radiation Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Biology
Iizuka, Daisuke
Yoshioka, Susumu
Kawai, Hidehiko
Okazaki, Emi
Kiriyama, Keita
Izumi, Shunsuke
Nishimura, Mayumi
Shimada, Yoshiya
Kamiya, Kenji
Suzuki, Fumio
Hepcidin-2 in mouse urine as a candidate radiation-responsive molecule
title Hepcidin-2 in mouse urine as a candidate radiation-responsive molecule
title_full Hepcidin-2 in mouse urine as a candidate radiation-responsive molecule
title_fullStr Hepcidin-2 in mouse urine as a candidate radiation-responsive molecule
title_full_unstemmed Hepcidin-2 in mouse urine as a candidate radiation-responsive molecule
title_short Hepcidin-2 in mouse urine as a candidate radiation-responsive molecule
title_sort hepcidin-2 in mouse urine as a candidate radiation-responsive molecule
topic Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795955/
https://www.ncbi.nlm.nih.gov/pubmed/26826199
http://dx.doi.org/10.1093/jrr/rrv098
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