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Silica nanoparticles increase human adipose tissue-derived stem cell proliferation through ERK1/2 activation

BACKGROUND: Silicon dioxide composites have been found to enhance the mechanical properties of scaffolds and to support growth of human adipose tissue-derived stem cells (hADSCs) both in vitro and in vivo. Silica (silicon dioxide alone) exists as differently sized particles when suspended in culture...

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Autores principales: Kim, Ki Joo, Joe, Young Ae, Kim, Min Kyoung, Lee, Su Jin, Ryu, Yeon Hee, Cho, Dong-Woo, Rhie, Jong Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378289/
https://www.ncbi.nlm.nih.gov/pubmed/25848249
http://dx.doi.org/10.2147/IJN.S71925
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author Kim, Ki Joo
Joe, Young Ae
Kim, Min Kyoung
Lee, Su Jin
Ryu, Yeon Hee
Cho, Dong-Woo
Rhie, Jong Won
author_facet Kim, Ki Joo
Joe, Young Ae
Kim, Min Kyoung
Lee, Su Jin
Ryu, Yeon Hee
Cho, Dong-Woo
Rhie, Jong Won
author_sort Kim, Ki Joo
collection PubMed
description BACKGROUND: Silicon dioxide composites have been found to enhance the mechanical properties of scaffolds and to support growth of human adipose tissue-derived stem cells (hADSCs) both in vitro and in vivo. Silica (silicon dioxide alone) exists as differently sized particles when suspended in culture medium, but it is not clear whether particle size influences the beneficial effect of silicon dioxide on hADSCs. In this study, we examined the effect of different sized particles on growth and mitogen-activated protein kinase signaling in hADSCs. METHODS: Silica gel was prepared by a chemical reaction using hydrochloric acid and sodium silicate, washed, sterilized, and suspended in serum-free culture medium for 48 hours, and then sequentially filtered through a 0.22 μm filter (filtrate containing nanoparticles smaller than 220 nm; silica NPs). hADSCs were incubated with silica NPs or 3 μm silica microparticles (MPs), examined by transmission electron microscopy, and assayed for cell proliferation, apoptosis, and mitogen-activated protein kinase signaling. RESULTS: Eighty-nine percent of the silica NPs were around 50–120 nm in size. When hADSCs were treated with the study particles, silica NPs were observed in endocytosed vacuoles in the cytosol of hADSCs, but silica MPs showed no cell entry. Silica NPs increased the proliferation of hADSCs, but silica MPs had no significant effect in this regard. Instead, silica MPs induced slight apoptosis. Silica NPs increased phosphorylation of extracellular signal-related kinase (ERK)1/2, while silica MPs increased phosphorylation of p38. Silica NPs had no effect on phosphorylation of Janus kinase or p38. Pretreatment with PD98059, a MEK inhibitor, prevented the ERK1/2 phosphorylation and proliferation induced by silica NPs. CONCLUSION: Scaffolds containing silicon dioxide for tissue engineering may enhance cell growth through ERK1/2 activation only when NPs around 50–120 nm in size are included, and single component silica-derived NPs could be useful for bioscaffolds in stem cell therapy.
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spelling pubmed-43782892015-04-06 Silica nanoparticles increase human adipose tissue-derived stem cell proliferation through ERK1/2 activation Kim, Ki Joo Joe, Young Ae Kim, Min Kyoung Lee, Su Jin Ryu, Yeon Hee Cho, Dong-Woo Rhie, Jong Won Int J Nanomedicine Original Research BACKGROUND: Silicon dioxide composites have been found to enhance the mechanical properties of scaffolds and to support growth of human adipose tissue-derived stem cells (hADSCs) both in vitro and in vivo. Silica (silicon dioxide alone) exists as differently sized particles when suspended in culture medium, but it is not clear whether particle size influences the beneficial effect of silicon dioxide on hADSCs. In this study, we examined the effect of different sized particles on growth and mitogen-activated protein kinase signaling in hADSCs. METHODS: Silica gel was prepared by a chemical reaction using hydrochloric acid and sodium silicate, washed, sterilized, and suspended in serum-free culture medium for 48 hours, and then sequentially filtered through a 0.22 μm filter (filtrate containing nanoparticles smaller than 220 nm; silica NPs). hADSCs were incubated with silica NPs or 3 μm silica microparticles (MPs), examined by transmission electron microscopy, and assayed for cell proliferation, apoptosis, and mitogen-activated protein kinase signaling. RESULTS: Eighty-nine percent of the silica NPs were around 50–120 nm in size. When hADSCs were treated with the study particles, silica NPs were observed in endocytosed vacuoles in the cytosol of hADSCs, but silica MPs showed no cell entry. Silica NPs increased the proliferation of hADSCs, but silica MPs had no significant effect in this regard. Instead, silica MPs induced slight apoptosis. Silica NPs increased phosphorylation of extracellular signal-related kinase (ERK)1/2, while silica MPs increased phosphorylation of p38. Silica NPs had no effect on phosphorylation of Janus kinase or p38. Pretreatment with PD98059, a MEK inhibitor, prevented the ERK1/2 phosphorylation and proliferation induced by silica NPs. CONCLUSION: Scaffolds containing silicon dioxide for tissue engineering may enhance cell growth through ERK1/2 activation only when NPs around 50–120 nm in size are included, and single component silica-derived NPs could be useful for bioscaffolds in stem cell therapy. Dove Medical Press 2015-03-24 /pmc/articles/PMC4378289/ /pubmed/25848249 http://dx.doi.org/10.2147/IJN.S71925 Text en © 2015 Kim et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. 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
Kim, Ki Joo
Joe, Young Ae
Kim, Min Kyoung
Lee, Su Jin
Ryu, Yeon Hee
Cho, Dong-Woo
Rhie, Jong Won
Silica nanoparticles increase human adipose tissue-derived stem cell proliferation through ERK1/2 activation
title Silica nanoparticles increase human adipose tissue-derived stem cell proliferation through ERK1/2 activation
title_full Silica nanoparticles increase human adipose tissue-derived stem cell proliferation through ERK1/2 activation
title_fullStr Silica nanoparticles increase human adipose tissue-derived stem cell proliferation through ERK1/2 activation
title_full_unstemmed Silica nanoparticles increase human adipose tissue-derived stem cell proliferation through ERK1/2 activation
title_short Silica nanoparticles increase human adipose tissue-derived stem cell proliferation through ERK1/2 activation
title_sort silica nanoparticles increase human adipose tissue-derived stem cell proliferation through erk1/2 activation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378289/
https://www.ncbi.nlm.nih.gov/pubmed/25848249
http://dx.doi.org/10.2147/IJN.S71925
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