Nutritional deprivation and LPS exposure as feasible methods for induction of cellular - A methodology to validate for vitro photobiomodulation studies

Detalhes bibliográficos
Autor(a) principal: Basso, F. G. [UNESP]
Data de Publicação: 2016
Outros Autores: Turrioni, A. P. S. [UNESP], Almeida, L. F. [UNESP], Soares, D. G. [UNESP], Oliveira, C. F., Hebling, J. [UNESP], Souza Costa, C. A. de [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.jphotobiol.2016.04.001
http://hdl.handle.net/11449/158895
Resumo: Previous studies have demonstrated that high biostimulation takes place when cells under stress are subjected to phototherapy by laser or light-emitting-diode (LED) devices. Several studies selected nutritional deprivation by reducing the concentration of fetal bovine serum (FBS) in the culture medium or the exposure of cultured cells to lipopolysaccharide (LPS) as an in vitro cellular stress condition. However, there are no data certifying that these stimuli cause stressful conditions for cultured cells. This investigation assessed the induction of cellular stress by decreasing the concentration of FBS or adding LPS to culture medium. Odontoblast-like cells (MDPC-23) were cultured in complete culture medium (DMEM) containing 10% FBS. After a 12-hour incubation period, the DMEM was replaced by fresh medium containing 10% FBS (control), low concentrations of FBS (0, 0.2, 0.5, 2, or 5%) or LPS from Escherichia coli (10 mu g/ml). After an additional 12-hour incubation, cell viability, total cell-counting, total protein production, and gene expression of heat shock protein 70 (HSP70) were assessed. Data were statistically analyzed by ANOVA complemented by the Tukey test, with 5% considered significant. Cell viability was negatively affected only for 0% FBS, while reduced viable cell numbers and total protein production were detected for FBS concentrations lower than 2%. Higher HSP70 gene expression was also observed for FBS concentrations lower than 2% and for cells exposed to LPS. The nutritional deprivation model with culture medium lower than 2% of FBS can be safely used to induce cellular stress for in vitro photobiomodulation studies. (C) 2016 Elsevier B.V. All rights reserved.
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spelling Nutritional deprivation and LPS exposure as feasible methods for induction of cellular - A methodology to validate for vitro photobiomodulation studiesPhototherapyCellular stressHeat shock proteinLPSPrevious studies have demonstrated that high biostimulation takes place when cells under stress are subjected to phototherapy by laser or light-emitting-diode (LED) devices. Several studies selected nutritional deprivation by reducing the concentration of fetal bovine serum (FBS) in the culture medium or the exposure of cultured cells to lipopolysaccharide (LPS) as an in vitro cellular stress condition. However, there are no data certifying that these stimuli cause stressful conditions for cultured cells. This investigation assessed the induction of cellular stress by decreasing the concentration of FBS or adding LPS to culture medium. Odontoblast-like cells (MDPC-23) were cultured in complete culture medium (DMEM) containing 10% FBS. After a 12-hour incubation period, the DMEM was replaced by fresh medium containing 10% FBS (control), low concentrations of FBS (0, 0.2, 0.5, 2, or 5%) or LPS from Escherichia coli (10 mu g/ml). After an additional 12-hour incubation, cell viability, total cell-counting, total protein production, and gene expression of heat shock protein 70 (HSP70) were assessed. Data were statistically analyzed by ANOVA complemented by the Tukey test, with 5% considered significant. Cell viability was negatively affected only for 0% FBS, while reduced viable cell numbers and total protein production were detected for FBS concentrations lower than 2%. Higher HSP70 gene expression was also observed for FBS concentrations lower than 2% and for cells exposed to LPS. The nutritional deprivation model with culture medium lower than 2% of FBS can be safely used to induce cellular stress for in vitro photobiomodulation studies. (C) 2016 Elsevier B.V. All rights reserved.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Universidade Estadual de Sao Paulo - UNESP (PROINTER - PROPe/PROPG)Univ Estadual Paulista, Araraquara Sch Dent, Araraquara, SP, BrazilUniv Ribeirao Preto, UNAERP, Ribeirao Preto, SP, BrazilUniv Estadual Paulista, Araraquara Sch Dent, Araraquara, SP, BrazilFAPESP: 2013/05879-0FAPESP: PD: 2012/17947-8CNPq: 303599/2014-6Universidade Estadual de Sao Paulo - UNESP (PROINTER - PROPe/PROPG): 907 - PROINTER - PROPe/PROPGElsevier B.V.Universidade Estadual Paulista (Unesp)Univ Ribeirao PretoBasso, F. G. [UNESP]Turrioni, A. P. S. [UNESP]Almeida, L. F. [UNESP]Soares, D. G. [UNESP]Oliveira, C. F.Hebling, J. [UNESP]Souza Costa, C. A. de [UNESP]2018-11-26T15:29:42Z2018-11-26T15:29:42Z2016-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article205-210application/pdfhttp://dx.doi.org/10.1016/j.jphotobiol.2016.04.001Journal Of Photochemistry And Photobiology B-biology. Lausanne: Elsevier Science Sa, v. 159, p. 205-210, 2016.1011-1344http://hdl.handle.net/11449/15889510.1016/j.jphotobiol.2016.04.001WOS:000376702400030WOS000376702400030.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Photochemistry And Photobiology B-biology0,698info:eu-repo/semantics/openAccess2023-10-22T06:06:03Zoai:repositorio.unesp.br:11449/158895Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:35:19.378889Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Nutritional deprivation and LPS exposure as feasible methods for induction of cellular - A methodology to validate for vitro photobiomodulation studies
title Nutritional deprivation and LPS exposure as feasible methods for induction of cellular - A methodology to validate for vitro photobiomodulation studies
spellingShingle Nutritional deprivation and LPS exposure as feasible methods for induction of cellular - A methodology to validate for vitro photobiomodulation studies
Basso, F. G. [UNESP]
Phototherapy
Cellular stress
Heat shock protein
LPS
title_short Nutritional deprivation and LPS exposure as feasible methods for induction of cellular - A methodology to validate for vitro photobiomodulation studies
title_full Nutritional deprivation and LPS exposure as feasible methods for induction of cellular - A methodology to validate for vitro photobiomodulation studies
title_fullStr Nutritional deprivation and LPS exposure as feasible methods for induction of cellular - A methodology to validate for vitro photobiomodulation studies
title_full_unstemmed Nutritional deprivation and LPS exposure as feasible methods for induction of cellular - A methodology to validate for vitro photobiomodulation studies
title_sort Nutritional deprivation and LPS exposure as feasible methods for induction of cellular - A methodology to validate for vitro photobiomodulation studies
author Basso, F. G. [UNESP]
author_facet Basso, F. G. [UNESP]
Turrioni, A. P. S. [UNESP]
Almeida, L. F. [UNESP]
Soares, D. G. [UNESP]
Oliveira, C. F.
Hebling, J. [UNESP]
Souza Costa, C. A. de [UNESP]
author_role author
author2 Turrioni, A. P. S. [UNESP]
Almeida, L. F. [UNESP]
Soares, D. G. [UNESP]
Oliveira, C. F.
Hebling, J. [UNESP]
Souza Costa, C. A. de [UNESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Univ Ribeirao Preto
dc.contributor.author.fl_str_mv Basso, F. G. [UNESP]
Turrioni, A. P. S. [UNESP]
Almeida, L. F. [UNESP]
Soares, D. G. [UNESP]
Oliveira, C. F.
Hebling, J. [UNESP]
Souza Costa, C. A. de [UNESP]
dc.subject.por.fl_str_mv Phototherapy
Cellular stress
Heat shock protein
LPS
topic Phototherapy
Cellular stress
Heat shock protein
LPS
description Previous studies have demonstrated that high biostimulation takes place when cells under stress are subjected to phototherapy by laser or light-emitting-diode (LED) devices. Several studies selected nutritional deprivation by reducing the concentration of fetal bovine serum (FBS) in the culture medium or the exposure of cultured cells to lipopolysaccharide (LPS) as an in vitro cellular stress condition. However, there are no data certifying that these stimuli cause stressful conditions for cultured cells. This investigation assessed the induction of cellular stress by decreasing the concentration of FBS or adding LPS to culture medium. Odontoblast-like cells (MDPC-23) were cultured in complete culture medium (DMEM) containing 10% FBS. After a 12-hour incubation period, the DMEM was replaced by fresh medium containing 10% FBS (control), low concentrations of FBS (0, 0.2, 0.5, 2, or 5%) or LPS from Escherichia coli (10 mu g/ml). After an additional 12-hour incubation, cell viability, total cell-counting, total protein production, and gene expression of heat shock protein 70 (HSP70) were assessed. Data were statistically analyzed by ANOVA complemented by the Tukey test, with 5% considered significant. Cell viability was negatively affected only for 0% FBS, while reduced viable cell numbers and total protein production were detected for FBS concentrations lower than 2%. Higher HSP70 gene expression was also observed for FBS concentrations lower than 2% and for cells exposed to LPS. The nutritional deprivation model with culture medium lower than 2% of FBS can be safely used to induce cellular stress for in vitro photobiomodulation studies. (C) 2016 Elsevier B.V. All rights reserved.
publishDate 2016
dc.date.none.fl_str_mv 2016-06-01
2018-11-26T15:29:42Z
2018-11-26T15:29:42Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.jphotobiol.2016.04.001
Journal Of Photochemistry And Photobiology B-biology. Lausanne: Elsevier Science Sa, v. 159, p. 205-210, 2016.
1011-1344
http://hdl.handle.net/11449/158895
10.1016/j.jphotobiol.2016.04.001
WOS:000376702400030
WOS000376702400030.pdf
url http://dx.doi.org/10.1016/j.jphotobiol.2016.04.001
http://hdl.handle.net/11449/158895
identifier_str_mv Journal Of Photochemistry And Photobiology B-biology. Lausanne: Elsevier Science Sa, v. 159, p. 205-210, 2016.
1011-1344
10.1016/j.jphotobiol.2016.04.001
WOS:000376702400030
WOS000376702400030.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal Of Photochemistry And Photobiology B-biology
0,698
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 205-210
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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