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MnSOD downregulation induced by extremely low 0.1 mGy single and fractionated X-rays and microgravity treatment in human neuroblastoma cell line, NB-1

A human neuroblastoma cell line, NB-1, was treated with 24 h of microgravity simulation by clinostat, or irradiated with extremely small X-ray doses of 0.1 or 1.0 mGy using single and 10 times fractionation regimes with 1 and 2 h time-intervals. A quantitative real-time reverse transcription polymer...

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Autores principales: Indo, Hiroko P., Tomiyoshi, Tsukasa, Suenaga, Shigeaki, Tomita, Kazuo, Suzuki, Hiromi, Masuda, Daisuke, Terada, Masahiro, Ishioka, Noriaki, Gusev, Oleg, Cornette, Richard, Okuda, Takashi, Mukai, Chiaki, Majima, Hideyuki J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: the Society for Free Radical Research Japan 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4566025/
https://www.ncbi.nlm.nih.gov/pubmed/26388666
http://dx.doi.org/10.3164/jcbn.15-20
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author Indo, Hiroko P.
Tomiyoshi, Tsukasa
Suenaga, Shigeaki
Tomita, Kazuo
Suzuki, Hiromi
Masuda, Daisuke
Terada, Masahiro
Ishioka, Noriaki
Gusev, Oleg
Cornette, Richard
Okuda, Takashi
Mukai, Chiaki
Majima, Hideyuki J.
author_facet Indo, Hiroko P.
Tomiyoshi, Tsukasa
Suenaga, Shigeaki
Tomita, Kazuo
Suzuki, Hiromi
Masuda, Daisuke
Terada, Masahiro
Ishioka, Noriaki
Gusev, Oleg
Cornette, Richard
Okuda, Takashi
Mukai, Chiaki
Majima, Hideyuki J.
author_sort Indo, Hiroko P.
collection PubMed
description A human neuroblastoma cell line, NB-1, was treated with 24 h of microgravity simulation by clinostat, or irradiated with extremely small X-ray doses of 0.1 or 1.0 mGy using single and 10 times fractionation regimes with 1 and 2 h time-intervals. A quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR) examination was performed for apoptosis related factors (BAX, CYTC, APAF1, VDAC1–3, CASP3, CASP8, CASP9 P53, AIF, ANT1 and 2, BCL2, MnSOD, autophagy related BECN and necrosis related CYP-40. The qRT-PCR results revealed that microgravity did not result in significant changes except for a upregulation of proapoptotic VDAC2, and downregulations of proapoptotic CASP9 and antiapoptotic MnSOD. After 0.1 mGy fractionation irradiation, there was increased expression of proapoptotic APAF1 and downregulation of proapoptotic CYTC, VDAC2, VDAC3, CASP8, AIF, ANT1, and ANT2, as well as an increase in expression of antiapoptotic BCL2. There was also a decrease in MnSOD expression with 0.1 mGy fractionation irradiation. These results suggest that microgravity and low-dose radiation may decrease apoptosis but may potentially increase oxidative stress.
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spelling pubmed-45660252015-09-18 MnSOD downregulation induced by extremely low 0.1 mGy single and fractionated X-rays and microgravity treatment in human neuroblastoma cell line, NB-1 Indo, Hiroko P. Tomiyoshi, Tsukasa Suenaga, Shigeaki Tomita, Kazuo Suzuki, Hiromi Masuda, Daisuke Terada, Masahiro Ishioka, Noriaki Gusev, Oleg Cornette, Richard Okuda, Takashi Mukai, Chiaki Majima, Hideyuki J. J Clin Biochem Nutr Original Article A human neuroblastoma cell line, NB-1, was treated with 24 h of microgravity simulation by clinostat, or irradiated with extremely small X-ray doses of 0.1 or 1.0 mGy using single and 10 times fractionation regimes with 1 and 2 h time-intervals. A quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR) examination was performed for apoptosis related factors (BAX, CYTC, APAF1, VDAC1–3, CASP3, CASP8, CASP9 P53, AIF, ANT1 and 2, BCL2, MnSOD, autophagy related BECN and necrosis related CYP-40. The qRT-PCR results revealed that microgravity did not result in significant changes except for a upregulation of proapoptotic VDAC2, and downregulations of proapoptotic CASP9 and antiapoptotic MnSOD. After 0.1 mGy fractionation irradiation, there was increased expression of proapoptotic APAF1 and downregulation of proapoptotic CYTC, VDAC2, VDAC3, CASP8, AIF, ANT1, and ANT2, as well as an increase in expression of antiapoptotic BCL2. There was also a decrease in MnSOD expression with 0.1 mGy fractionation irradiation. These results suggest that microgravity and low-dose radiation may decrease apoptosis but may potentially increase oxidative stress. the Society for Free Radical Research Japan 2015-09 2015-07-11 /pmc/articles/PMC4566025/ /pubmed/26388666 http://dx.doi.org/10.3164/jcbn.15-20 Text en Copyright © 2015 JCBN 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 Original Article
Indo, Hiroko P.
Tomiyoshi, Tsukasa
Suenaga, Shigeaki
Tomita, Kazuo
Suzuki, Hiromi
Masuda, Daisuke
Terada, Masahiro
Ishioka, Noriaki
Gusev, Oleg
Cornette, Richard
Okuda, Takashi
Mukai, Chiaki
Majima, Hideyuki J.
MnSOD downregulation induced by extremely low 0.1 mGy single and fractionated X-rays and microgravity treatment in human neuroblastoma cell line, NB-1
title MnSOD downregulation induced by extremely low 0.1 mGy single and fractionated X-rays and microgravity treatment in human neuroblastoma cell line, NB-1
title_full MnSOD downregulation induced by extremely low 0.1 mGy single and fractionated X-rays and microgravity treatment in human neuroblastoma cell line, NB-1
title_fullStr MnSOD downregulation induced by extremely low 0.1 mGy single and fractionated X-rays and microgravity treatment in human neuroblastoma cell line, NB-1
title_full_unstemmed MnSOD downregulation induced by extremely low 0.1 mGy single and fractionated X-rays and microgravity treatment in human neuroblastoma cell line, NB-1
title_short MnSOD downregulation induced by extremely low 0.1 mGy single and fractionated X-rays and microgravity treatment in human neuroblastoma cell line, NB-1
title_sort mnsod downregulation induced by extremely low 0.1 mgy single and fractionated x-rays and microgravity treatment in human neuroblastoma cell line, nb-1
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4566025/
https://www.ncbi.nlm.nih.gov/pubmed/26388666
http://dx.doi.org/10.3164/jcbn.15-20
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