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Cytoprotective effect of glutaraldehyde erythropoietin on HEK293 kidney cells after silver nanoparticle exposure

The toxic effects from exposure to silver nanoparticles (AgNPs), which are broadly present in many consumer products, have long raised concerns. Many studies have focused on the mechanisms of nanosilver, which cause toxicity in human cells, but little is known about prevention of this type of injury...

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Autores principales: Sooklert, Kanidta, Chattong, Supreecha, Manotham, Krissanapong, Boonwong, Chawikan, Klaharn, I-yanut, Jindatip, Depicha, Sereemaspun, Amornpun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4760275/
https://www.ncbi.nlm.nih.gov/pubmed/26929619
http://dx.doi.org/10.2147/IJN.S95654
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author Sooklert, Kanidta
Chattong, Supreecha
Manotham, Krissanapong
Boonwong, Chawikan
Klaharn, I-yanut
Jindatip, Depicha
Sereemaspun, Amornpun
author_facet Sooklert, Kanidta
Chattong, Supreecha
Manotham, Krissanapong
Boonwong, Chawikan
Klaharn, I-yanut
Jindatip, Depicha
Sereemaspun, Amornpun
author_sort Sooklert, Kanidta
collection PubMed
description The toxic effects from exposure to silver nanoparticles (AgNPs), which are broadly present in many consumer products, have long raised concerns. Many studies have focused on the mechanisms of nanosilver, which cause toxicity in human cells, but little is known about prevention of this type of injury. This study investigated the in vitro effects of glutaraldehyde erythropoietin (GEPO), a cytoprotective compound derived from erythropoietin, in terms of cell protection against AgNP-induced injury. HEK293 cells were pretreated with or without GEPO before administration of AgNPs. The protective effects of GEPO in this cell line were assessed by the percentage of viable cells, alterations of cell morphology, and the proliferative capability of the cells. In addition, we assessed the role of GEPO in lowering cellular oxidative stress and regulating expression of the anti-apoptotic protein Bcl2. The results showed rescue effects on the percentage of viable and proliferative cells among GEPO pretreated cells. Pretreatment with GEPO maintained the normal cell shape and ultrastructural morphology. Moreover, GEPO reduced the generation of reactive oxygen species in cells and activated expression of Bcl2, which are the major mechanisms in protection against cellular toxicity induced by AgNPs. In conclusion, our study showed that the cytotoxic effects from exposure to AgNPs can be prevented by GEPO.
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spelling pubmed-47602752016-02-29 Cytoprotective effect of glutaraldehyde erythropoietin on HEK293 kidney cells after silver nanoparticle exposure Sooklert, Kanidta Chattong, Supreecha Manotham, Krissanapong Boonwong, Chawikan Klaharn, I-yanut Jindatip, Depicha Sereemaspun, Amornpun Int J Nanomedicine Original Research The toxic effects from exposure to silver nanoparticles (AgNPs), which are broadly present in many consumer products, have long raised concerns. Many studies have focused on the mechanisms of nanosilver, which cause toxicity in human cells, but little is known about prevention of this type of injury. This study investigated the in vitro effects of glutaraldehyde erythropoietin (GEPO), a cytoprotective compound derived from erythropoietin, in terms of cell protection against AgNP-induced injury. HEK293 cells were pretreated with or without GEPO before administration of AgNPs. The protective effects of GEPO in this cell line were assessed by the percentage of viable cells, alterations of cell morphology, and the proliferative capability of the cells. In addition, we assessed the role of GEPO in lowering cellular oxidative stress and regulating expression of the anti-apoptotic protein Bcl2. The results showed rescue effects on the percentage of viable and proliferative cells among GEPO pretreated cells. Pretreatment with GEPO maintained the normal cell shape and ultrastructural morphology. Moreover, GEPO reduced the generation of reactive oxygen species in cells and activated expression of Bcl2, which are the major mechanisms in protection against cellular toxicity induced by AgNPs. In conclusion, our study showed that the cytotoxic effects from exposure to AgNPs can be prevented by GEPO. Dove Medical Press 2016-02-12 /pmc/articles/PMC4760275/ /pubmed/26929619 http://dx.doi.org/10.2147/IJN.S95654 Text en © 2016 Sooklert et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Sooklert, Kanidta
Chattong, Supreecha
Manotham, Krissanapong
Boonwong, Chawikan
Klaharn, I-yanut
Jindatip, Depicha
Sereemaspun, Amornpun
Cytoprotective effect of glutaraldehyde erythropoietin on HEK293 kidney cells after silver nanoparticle exposure
title Cytoprotective effect of glutaraldehyde erythropoietin on HEK293 kidney cells after silver nanoparticle exposure
title_full Cytoprotective effect of glutaraldehyde erythropoietin on HEK293 kidney cells after silver nanoparticle exposure
title_fullStr Cytoprotective effect of glutaraldehyde erythropoietin on HEK293 kidney cells after silver nanoparticle exposure
title_full_unstemmed Cytoprotective effect of glutaraldehyde erythropoietin on HEK293 kidney cells after silver nanoparticle exposure
title_short Cytoprotective effect of glutaraldehyde erythropoietin on HEK293 kidney cells after silver nanoparticle exposure
title_sort cytoprotective effect of glutaraldehyde erythropoietin on hek293 kidney cells after silver nanoparticle exposure
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4760275/
https://www.ncbi.nlm.nih.gov/pubmed/26929619
http://dx.doi.org/10.2147/IJN.S95654
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