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Comparative effect of selenium and glycine on hydrogen peroxide-induced cell death and activation of macrophage U937 cells
The effects of selenium and glycine (either separately or in combination) on hydrogen peroxide-induced cell death on U937 cells and activation of U937-derived macrophages were investigated. In the first instance, U937 cells were incubated with or without selenium (Se) or glycine (GLY) or both (Se + ...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academy of Scientific Research and Technology, Egypt
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296632/ https://www.ncbi.nlm.nih.gov/pubmed/30647695 http://dx.doi.org/10.1016/j.jgeb.2017.06.006 |
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author | Ndoni, Solomon A Okoko, Tebekeme |
author_facet | Ndoni, Solomon A Okoko, Tebekeme |
author_sort | Ndoni, Solomon A |
collection | PubMed |
description | The effects of selenium and glycine (either separately or in combination) on hydrogen peroxide-induced cell death on U937 cells and activation of U937-derived macrophages were investigated. In the first instance, U937 cells were incubated with or without selenium (Se) or glycine (GLY) or both (Se + GLY) for 24 h before exposure to hydrogen peroxide. Control cells were not incubated with Se, GLY or exposed to hydrogen peroxide. Cell viability was later assessed via trypan blue and MTT assays. For the other experiment, U937 cells were transformed to the macrophage form using phorbol 12-myristate 13-acetate before incubating with or without Se, GLY, Se + GLY. Contents were subsequently exposed to hydrogen peroxide and 24 h later assessed for the production of TNF-α, IL-1, IL-6 and the expression of iNOS and NF-κB. The results revealed that hydrogen peroxide caused significant cell death which was ameliorated by both Se and GLY. Pre-incubation of the cells with both Se and GLY did not significantly enhance cell numbers compared to GLY (p > 0.05). On the other hand, Se and GLY reduced hydrogen peroxide-mediated production of TNF-α, IL-1, IL-6 and expression of iNOS and NF-κB. Incubating the U937-derived macrophages with Se + GLY significantly ameliorated hydrogen peroxide-mediated activation of macrophages when compared to pre-treatments with Se or GLY (p < 0.05). The findings demonstrate that both Se and GLY reduced hydrogen peroxide-induced alterations in U937 cells and U937-derived macrophages. Implications of the findings are discussed. |
format | Online Article Text |
id | pubmed-6296632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Academy of Scientific Research and Technology, Egypt |
record_format | MEDLINE/PubMed |
spelling | pubmed-62966322019-01-15 Comparative effect of selenium and glycine on hydrogen peroxide-induced cell death and activation of macrophage U937 cells Ndoni, Solomon A Okoko, Tebekeme J Genet Eng Biotechnol Others (In silico & Biochemistry) The effects of selenium and glycine (either separately or in combination) on hydrogen peroxide-induced cell death on U937 cells and activation of U937-derived macrophages were investigated. In the first instance, U937 cells were incubated with or without selenium (Se) or glycine (GLY) or both (Se + GLY) for 24 h before exposure to hydrogen peroxide. Control cells were not incubated with Se, GLY or exposed to hydrogen peroxide. Cell viability was later assessed via trypan blue and MTT assays. For the other experiment, U937 cells were transformed to the macrophage form using phorbol 12-myristate 13-acetate before incubating with or without Se, GLY, Se + GLY. Contents were subsequently exposed to hydrogen peroxide and 24 h later assessed for the production of TNF-α, IL-1, IL-6 and the expression of iNOS and NF-κB. The results revealed that hydrogen peroxide caused significant cell death which was ameliorated by both Se and GLY. Pre-incubation of the cells with both Se and GLY did not significantly enhance cell numbers compared to GLY (p > 0.05). On the other hand, Se and GLY reduced hydrogen peroxide-mediated production of TNF-α, IL-1, IL-6 and expression of iNOS and NF-κB. Incubating the U937-derived macrophages with Se + GLY significantly ameliorated hydrogen peroxide-mediated activation of macrophages when compared to pre-treatments with Se or GLY (p < 0.05). The findings demonstrate that both Se and GLY reduced hydrogen peroxide-induced alterations in U937 cells and U937-derived macrophages. Implications of the findings are discussed. Academy of Scientific Research and Technology, Egypt 2017-12 2017-06-27 /pmc/articles/PMC6296632/ /pubmed/30647695 http://dx.doi.org/10.1016/j.jgeb.2017.06.006 Text en © 2017 Production and hosting by Elsevier B.V. on behalf of Academy of Scientific Research & Technology. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Others (In silico & Biochemistry) Ndoni, Solomon A Okoko, Tebekeme Comparative effect of selenium and glycine on hydrogen peroxide-induced cell death and activation of macrophage U937 cells |
title | Comparative effect of selenium and glycine on hydrogen peroxide-induced cell death and activation of macrophage U937 cells |
title_full | Comparative effect of selenium and glycine on hydrogen peroxide-induced cell death and activation of macrophage U937 cells |
title_fullStr | Comparative effect of selenium and glycine on hydrogen peroxide-induced cell death and activation of macrophage U937 cells |
title_full_unstemmed | Comparative effect of selenium and glycine on hydrogen peroxide-induced cell death and activation of macrophage U937 cells |
title_short | Comparative effect of selenium and glycine on hydrogen peroxide-induced cell death and activation of macrophage U937 cells |
title_sort | comparative effect of selenium and glycine on hydrogen peroxide-induced cell death and activation of macrophage u937 cells |
topic | Others (In silico & Biochemistry) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296632/ https://www.ncbi.nlm.nih.gov/pubmed/30647695 http://dx.doi.org/10.1016/j.jgeb.2017.06.006 |
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