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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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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. |
format | Online Article Text |
id | pubmed-4795955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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