Nutritional deprivation and LPS exposure as feasible methods for induction of cellular - A methodology to validate for vitro photobiomodulation studies
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , |
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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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) |
repository.mail.fl_str_mv |
|
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1808128537336479744 |