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Apoptosis gene reprograming of human peripheral blood mononuclear cells induced by radioiodine-131 ((131)I) irradiation

BACKGROUND & OBJECTIVES: The nature of adaptable change of B-cell lymphoma-2 (BCL-2) and/or Bcl2-associated X protein (BAX) gene expression in the human peripheral blood mononuclear cells (PBMCs) irradiated by radioiodine in thyroid diseases therapy is not fully understood. In this study, the al...

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Autores principales: Li, Jian-Fang, Xie, Liang-Jun, Qin, Lu-Ping, Liu, Yi-Fei, Zhang, Ting-Jie, Huang, Yong, Cheng, Mu-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6702702/
https://www.ncbi.nlm.nih.gov/pubmed/31417030
http://dx.doi.org/10.4103/ijmr.IJMR_1455_17
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author Li, Jian-Fang
Xie, Liang-Jun
Qin, Lu-Ping
Liu, Yi-Fei
Zhang, Ting-Jie
Huang, Yong
Cheng, Mu-Hua
author_facet Li, Jian-Fang
Xie, Liang-Jun
Qin, Lu-Ping
Liu, Yi-Fei
Zhang, Ting-Jie
Huang, Yong
Cheng, Mu-Hua
author_sort Li, Jian-Fang
collection PubMed
description BACKGROUND & OBJECTIVES: The nature of adaptable change of B-cell lymphoma-2 (BCL-2) and/or Bcl2-associated X protein (BAX) gene expression in the human peripheral blood mononuclear cells (PBMCs) irradiated by radioiodine in thyroid diseases therapy is not fully understood. In this study, the alternation of apoptotic gene expression was evaluated while the PBMCs collected from healthy volunteers were irradiated by the radioiodine-131 ((131)I). METHODS: Fasting blood samples were obtained from healthy volunteers. PBMCs from group 0 to 6 were incubated and exposed to different doses of (131)I in cell suspension for 6, 12, 24 and 48 h. The apoptosis rates and expression of BCL-2 and BAX genes of PBMCs were examined. RESULTS: The apoptosis rate in the human PBMCs was gradually enhanced after six hour irradiation. The values of BCL-2 and BAX gene expression in groups 1-6 were higher than in group 0 within 6 h of irradiation, and then, these were decreased gradually from 6 to 12 h. BCL-2 gene expression increased in groups 1-3 after 12 h irradiation, but there was no difference in groups 4-6. The ratio of BCL-2/BAX gene expression among groups 4-6 gradually decreased during the period from 6 to 12 h, and it was significantly lower than in the group 0 at 12, 24 and 48 h. INTERPRETATION & CONCLUSIONS: The expression of BCL-2 and BAX genes was initially upregulated following irradiation. Later, the balance of BCL-2/BAX genes expression was adjusted, and then, PBMCs underwent apoptosis at higher doses of radiation.
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spelling pubmed-67027022019-09-06 Apoptosis gene reprograming of human peripheral blood mononuclear cells induced by radioiodine-131 ((131)I) irradiation Li, Jian-Fang Xie, Liang-Jun Qin, Lu-Ping Liu, Yi-Fei Zhang, Ting-Jie Huang, Yong Cheng, Mu-Hua Indian J Med Res Original Article BACKGROUND & OBJECTIVES: The nature of adaptable change of B-cell lymphoma-2 (BCL-2) and/or Bcl2-associated X protein (BAX) gene expression in the human peripheral blood mononuclear cells (PBMCs) irradiated by radioiodine in thyroid diseases therapy is not fully understood. In this study, the alternation of apoptotic gene expression was evaluated while the PBMCs collected from healthy volunteers were irradiated by the radioiodine-131 ((131)I). METHODS: Fasting blood samples were obtained from healthy volunteers. PBMCs from group 0 to 6 were incubated and exposed to different doses of (131)I in cell suspension for 6, 12, 24 and 48 h. The apoptosis rates and expression of BCL-2 and BAX genes of PBMCs were examined. RESULTS: The apoptosis rate in the human PBMCs was gradually enhanced after six hour irradiation. The values of BCL-2 and BAX gene expression in groups 1-6 were higher than in group 0 within 6 h of irradiation, and then, these were decreased gradually from 6 to 12 h. BCL-2 gene expression increased in groups 1-3 after 12 h irradiation, but there was no difference in groups 4-6. The ratio of BCL-2/BAX gene expression among groups 4-6 gradually decreased during the period from 6 to 12 h, and it was significantly lower than in the group 0 at 12, 24 and 48 h. INTERPRETATION & CONCLUSIONS: The expression of BCL-2 and BAX genes was initially upregulated following irradiation. Later, the balance of BCL-2/BAX genes expression was adjusted, and then, PBMCs underwent apoptosis at higher doses of radiation. Wolters Kluwer - Medknow 2019-05 /pmc/articles/PMC6702702/ /pubmed/31417030 http://dx.doi.org/10.4103/ijmr.IJMR_1455_17 Text en Copyright: © 2019 Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Li, Jian-Fang
Xie, Liang-Jun
Qin, Lu-Ping
Liu, Yi-Fei
Zhang, Ting-Jie
Huang, Yong
Cheng, Mu-Hua
Apoptosis gene reprograming of human peripheral blood mononuclear cells induced by radioiodine-131 ((131)I) irradiation
title Apoptosis gene reprograming of human peripheral blood mononuclear cells induced by radioiodine-131 ((131)I) irradiation
title_full Apoptosis gene reprograming of human peripheral blood mononuclear cells induced by radioiodine-131 ((131)I) irradiation
title_fullStr Apoptosis gene reprograming of human peripheral blood mononuclear cells induced by radioiodine-131 ((131)I) irradiation
title_full_unstemmed Apoptosis gene reprograming of human peripheral blood mononuclear cells induced by radioiodine-131 ((131)I) irradiation
title_short Apoptosis gene reprograming of human peripheral blood mononuclear cells induced by radioiodine-131 ((131)I) irradiation
title_sort apoptosis gene reprograming of human peripheral blood mononuclear cells induced by radioiodine-131 ((131)i) irradiation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6702702/
https://www.ncbi.nlm.nih.gov/pubmed/31417030
http://dx.doi.org/10.4103/ijmr.IJMR_1455_17
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