Low-level laser irradiation promotes proliferation of cryopreserved adipose-derived stem cells

Detalhes bibliográficos
Autor(a) principal: Ginani,Fernanda
Data de Publicação: 2017
Outros Autores: Soares,Diego Moura, Rocha,Hugo Alexandre de Oliveira, Barboza,Carlos Augusto Galvão
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Einstein (São Paulo)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082017000300334
Resumo: ABSTRACT Objective To evaluate the effect of low-level laser irradiation on proliferation and viability of murine adipose-derived stem cells previously submitted to cryopreservation. Methods Adipose-derived stem cells were isolated from inguinal fat pads of three mice, submitted to cryopreservation in fetal bovine serum with 10% dimethylsulfoxide for 30 days and then thawed and maintained in normal culture conditions. Culture cells were either irradiated or not (control) with an InGaAIP diode laser at zero and 48 hours, using two different energy densities (0.5 and 1.0J/cm2). Cell proliferation was evaluated by trypan blue exclusion method and MTT assay at intervals of zero, 24, 48, and 72 hours after the first laser application. Cell viability and apoptosis of previously cryopreserved cells submitted to laser therapy were evaluated by flow cytometry. Results The Irradiated Groups (0.5 and 1.0J/cm2) showed an increased cell proliferation (p<0.05) when compared to the Control Group, however no significant difference between the two energy densities was observed. Flow cytometry revealed a percentage of viable cells higher than 99% in all groups. Conclusion Low-level laser irradiation has stimulatory effects on the proliferation of adipose-derived stem cells previously submitted to cryopreservation.
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spelling Low-level laser irradiation promotes proliferation of cryopreserved adipose-derived stem cellsAdipose tissueCryopreservationLaser therapyStem cellsCell proliferationABSTRACT Objective To evaluate the effect of low-level laser irradiation on proliferation and viability of murine adipose-derived stem cells previously submitted to cryopreservation. Methods Adipose-derived stem cells were isolated from inguinal fat pads of three mice, submitted to cryopreservation in fetal bovine serum with 10% dimethylsulfoxide for 30 days and then thawed and maintained in normal culture conditions. Culture cells were either irradiated or not (control) with an InGaAIP diode laser at zero and 48 hours, using two different energy densities (0.5 and 1.0J/cm2). Cell proliferation was evaluated by trypan blue exclusion method and MTT assay at intervals of zero, 24, 48, and 72 hours after the first laser application. Cell viability and apoptosis of previously cryopreserved cells submitted to laser therapy were evaluated by flow cytometry. Results The Irradiated Groups (0.5 and 1.0J/cm2) showed an increased cell proliferation (p<0.05) when compared to the Control Group, however no significant difference between the two energy densities was observed. Flow cytometry revealed a percentage of viable cells higher than 99% in all groups. Conclusion Low-level laser irradiation has stimulatory effects on the proliferation of adipose-derived stem cells previously submitted to cryopreservation.Instituto Israelita de Ensino e Pesquisa Albert Einstein2017-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082017000300334einstein (São Paulo) v.15 n.3 2017reponame:Einstein (São Paulo)instname:Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)instacron:IIEPAE10.1590/s1679-45082017ao3991info:eu-repo/semantics/openAccessGinani,FernandaSoares,Diego MouraRocha,Hugo Alexandre de OliveiraBarboza,Carlos Augusto Galvãoeng2017-10-26T00:00:00Zoai:scielo:S1679-45082017000300334Revistahttps://journal.einstein.br/pt-br/ONGhttps://old.scielo.br/oai/scielo-oai.php||revista@einstein.br2317-63851679-4508opendoar:2017-10-26T00:00Einstein (São Paulo) - Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)false
dc.title.none.fl_str_mv Low-level laser irradiation promotes proliferation of cryopreserved adipose-derived stem cells
title Low-level laser irradiation promotes proliferation of cryopreserved adipose-derived stem cells
spellingShingle Low-level laser irradiation promotes proliferation of cryopreserved adipose-derived stem cells
Ginani,Fernanda
Adipose tissue
Cryopreservation
Laser therapy
Stem cells
Cell proliferation
title_short Low-level laser irradiation promotes proliferation of cryopreserved adipose-derived stem cells
title_full Low-level laser irradiation promotes proliferation of cryopreserved adipose-derived stem cells
title_fullStr Low-level laser irradiation promotes proliferation of cryopreserved adipose-derived stem cells
title_full_unstemmed Low-level laser irradiation promotes proliferation of cryopreserved adipose-derived stem cells
title_sort Low-level laser irradiation promotes proliferation of cryopreserved adipose-derived stem cells
author Ginani,Fernanda
author_facet Ginani,Fernanda
Soares,Diego Moura
Rocha,Hugo Alexandre de Oliveira
Barboza,Carlos Augusto Galvão
author_role author
author2 Soares,Diego Moura
Rocha,Hugo Alexandre de Oliveira
Barboza,Carlos Augusto Galvão
author2_role author
author
author
dc.contributor.author.fl_str_mv Ginani,Fernanda
Soares,Diego Moura
Rocha,Hugo Alexandre de Oliveira
Barboza,Carlos Augusto Galvão
dc.subject.por.fl_str_mv Adipose tissue
Cryopreservation
Laser therapy
Stem cells
Cell proliferation
topic Adipose tissue
Cryopreservation
Laser therapy
Stem cells
Cell proliferation
description ABSTRACT Objective To evaluate the effect of low-level laser irradiation on proliferation and viability of murine adipose-derived stem cells previously submitted to cryopreservation. Methods Adipose-derived stem cells were isolated from inguinal fat pads of three mice, submitted to cryopreservation in fetal bovine serum with 10% dimethylsulfoxide for 30 days and then thawed and maintained in normal culture conditions. Culture cells were either irradiated or not (control) with an InGaAIP diode laser at zero and 48 hours, using two different energy densities (0.5 and 1.0J/cm2). Cell proliferation was evaluated by trypan blue exclusion method and MTT assay at intervals of zero, 24, 48, and 72 hours after the first laser application. Cell viability and apoptosis of previously cryopreserved cells submitted to laser therapy were evaluated by flow cytometry. Results The Irradiated Groups (0.5 and 1.0J/cm2) showed an increased cell proliferation (p<0.05) when compared to the Control Group, however no significant difference between the two energy densities was observed. Flow cytometry revealed a percentage of viable cells higher than 99% in all groups. Conclusion Low-level laser irradiation has stimulatory effects on the proliferation of adipose-derived stem cells previously submitted to cryopreservation.
publishDate 2017
dc.date.none.fl_str_mv 2017-09-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082017000300334
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082017000300334
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/s1679-45082017ao3991
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Instituto Israelita de Ensino e Pesquisa Albert Einstein
publisher.none.fl_str_mv Instituto Israelita de Ensino e Pesquisa Albert Einstein
dc.source.none.fl_str_mv einstein (São Paulo) v.15 n.3 2017
reponame:Einstein (São Paulo)
instname:Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)
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instname_str Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)
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reponame_str Einstein (São Paulo)
collection Einstein (São Paulo)
repository.name.fl_str_mv Einstein (São Paulo) - Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)
repository.mail.fl_str_mv ||revista@einstein.br
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