Prostaglandin E2 Induces Expression of Mineralization Genes by Undifferentiated Dental Pulp Cells
| Main Author: | |
|---|---|
| Publication Date: | 2019 |
| Other Authors: | , , , |
| Format: | Article |
| Language: | eng |
| Source: | Brazilian Dental Journal |
| Download full: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402019000300201 |
Summary: | Abstract Prostaglandin E2 (PGE2) is a lipid mediator usually released during inflammation. This study aimed to investigate the potential of soluble or microsphere-loaded PGE2 on inducing differentiation of dental pulp stem cells. PGE2-loaded microspheres (MS) were prepared using an oil-in-water emulsion solvent extraction-evaporation process and were characterized. Mouse dental pulp stem cells (OD-21) were stimulated with soluble or PGE2-loaded MS (0.01 and 0.1 µM). Cell viability was determined by MTT colorimetric assay. Ibsp, Bmp2 and Runx2 expression was measured by quantitative reverse transcription polymerase chain reaction (qRT-PCR) after 3, 6, and 24 h. The results showed that the soluble PGE2 reduced dental pulp stem cells viability after 24 h of stimulation whereas PGE2-loaded MS did not. Soluble PGE2 up-regulated Ibsp and Bmp2 at 3 h, differently from PGE2-loaded MS. On the other hand, PGE2-MS induced Bmp2 and Runx2 at 6 h and Ibsp at 24 h. In conclusion, our in vitro results show that PGE2, soluble or loaded in MS are not cytotoxic and modulateIbsp,Bmp2, andRunx2gene expression in cultured OD-21 cells. |
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Prostaglandin E2 Induces Expression of Mineralization Genes by Undifferentiated Dental Pulp Cellsmicrospheresprostaglandin E2dental pulp stem celldifferentiationAbstract Prostaglandin E2 (PGE2) is a lipid mediator usually released during inflammation. This study aimed to investigate the potential of soluble or microsphere-loaded PGE2 on inducing differentiation of dental pulp stem cells. PGE2-loaded microspheres (MS) were prepared using an oil-in-water emulsion solvent extraction-evaporation process and were characterized. Mouse dental pulp stem cells (OD-21) were stimulated with soluble or PGE2-loaded MS (0.01 and 0.1 µM). Cell viability was determined by MTT colorimetric assay. Ibsp, Bmp2 and Runx2 expression was measured by quantitative reverse transcription polymerase chain reaction (qRT-PCR) after 3, 6, and 24 h. The results showed that the soluble PGE2 reduced dental pulp stem cells viability after 24 h of stimulation whereas PGE2-loaded MS did not. Soluble PGE2 up-regulated Ibsp and Bmp2 at 3 h, differently from PGE2-loaded MS. On the other hand, PGE2-MS induced Bmp2 and Runx2 at 6 h and Ibsp at 24 h. In conclusion, our in vitro results show that PGE2, soluble or loaded in MS are not cytotoxic and modulateIbsp,Bmp2, andRunx2gene expression in cultured OD-21 cells.Fundação Odontológica de Ribeirão Preto2019-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402019000300201Brazilian Dental Journal v.30 n.3 2019reponame:Brazilian Dental Journalinstname:Fundação Odontológica de Ribeirão Preto (FUNORP)instacron:FUNORP10.1590/0103-6440201902542info:eu-repo/semantics/openAccessLorencetti-Silva,FrancinePereira,Priscilla Aparecida TartariMeirelles,Alyne Fávero GalvãoFaccioli,Lúcia HelenaPaula-Silva,Francisco Wanderley Garciaeng2019-06-06T00:00:00Zoai:scielo:S0103-64402019000300201Revistahttps://www.scielo.br/j/bdj/https://old.scielo.br/oai/scielo-oai.phpbdj@forp.usp.br||sergio@fosjc.unesp.br1806-47600103-6440opendoar:2019-06-06T00:00Brazilian Dental Journal - Fundação Odontológica de Ribeirão Preto (FUNORP)false |
| dc.title.none.fl_str_mv |
Prostaglandin E2 Induces Expression of Mineralization Genes by Undifferentiated Dental Pulp Cells |
| title |
Prostaglandin E2 Induces Expression of Mineralization Genes by Undifferentiated Dental Pulp Cells |
| spellingShingle |
Prostaglandin E2 Induces Expression of Mineralization Genes by Undifferentiated Dental Pulp Cells Lorencetti-Silva,Francine microspheres prostaglandin E2 dental pulp stem cell differentiation |
| title_short |
Prostaglandin E2 Induces Expression of Mineralization Genes by Undifferentiated Dental Pulp Cells |
| title_full |
Prostaglandin E2 Induces Expression of Mineralization Genes by Undifferentiated Dental Pulp Cells |
| title_fullStr |
Prostaglandin E2 Induces Expression of Mineralization Genes by Undifferentiated Dental Pulp Cells |
| title_full_unstemmed |
Prostaglandin E2 Induces Expression of Mineralization Genes by Undifferentiated Dental Pulp Cells |
| title_sort |
Prostaglandin E2 Induces Expression of Mineralization Genes by Undifferentiated Dental Pulp Cells |
| author |
Lorencetti-Silva,Francine |
| author_facet |
Lorencetti-Silva,Francine Pereira,Priscilla Aparecida Tartari Meirelles,Alyne Fávero Galvão Faccioli,Lúcia Helena Paula-Silva,Francisco Wanderley Garcia |
| author_role |
author |
| author2 |
Pereira,Priscilla Aparecida Tartari Meirelles,Alyne Fávero Galvão Faccioli,Lúcia Helena Paula-Silva,Francisco Wanderley Garcia |
| author2_role |
author author author author |
| dc.contributor.author.fl_str_mv |
Lorencetti-Silva,Francine Pereira,Priscilla Aparecida Tartari Meirelles,Alyne Fávero Galvão Faccioli,Lúcia Helena Paula-Silva,Francisco Wanderley Garcia |
| dc.subject.por.fl_str_mv |
microspheres prostaglandin E2 dental pulp stem cell differentiation |
| topic |
microspheres prostaglandin E2 dental pulp stem cell differentiation |
| description |
Abstract Prostaglandin E2 (PGE2) is a lipid mediator usually released during inflammation. This study aimed to investigate the potential of soluble or microsphere-loaded PGE2 on inducing differentiation of dental pulp stem cells. PGE2-loaded microspheres (MS) were prepared using an oil-in-water emulsion solvent extraction-evaporation process and were characterized. Mouse dental pulp stem cells (OD-21) were stimulated with soluble or PGE2-loaded MS (0.01 and 0.1 µM). Cell viability was determined by MTT colorimetric assay. Ibsp, Bmp2 and Runx2 expression was measured by quantitative reverse transcription polymerase chain reaction (qRT-PCR) after 3, 6, and 24 h. The results showed that the soluble PGE2 reduced dental pulp stem cells viability after 24 h of stimulation whereas PGE2-loaded MS did not. Soluble PGE2 up-regulated Ibsp and Bmp2 at 3 h, differently from PGE2-loaded MS. On the other hand, PGE2-MS induced Bmp2 and Runx2 at 6 h and Ibsp at 24 h. In conclusion, our in vitro results show that PGE2, soluble or loaded in MS are not cytotoxic and modulateIbsp,Bmp2, andRunx2gene expression in cultured OD-21 cells. |
| publishDate |
2019 |
| dc.date.none.fl_str_mv |
2019-06-01 |
| dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
| dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402019000300201 |
| url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402019000300201 |
| dc.language.iso.fl_str_mv |
eng |
| language |
eng |
| dc.relation.none.fl_str_mv |
10.1590/0103-6440201902542 |
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info:eu-repo/semantics/openAccess |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
text/html |
| dc.publisher.none.fl_str_mv |
Fundação Odontológica de Ribeirão Preto |
| publisher.none.fl_str_mv |
Fundação Odontológica de Ribeirão Preto |
| dc.source.none.fl_str_mv |
Brazilian Dental Journal v.30 n.3 2019 reponame:Brazilian Dental Journal instname:Fundação Odontológica de Ribeirão Preto (FUNORP) instacron:FUNORP |
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Fundação Odontológica de Ribeirão Preto (FUNORP) |
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FUNORP |
| institution |
FUNORP |
| reponame_str |
Brazilian Dental Journal |
| collection |
Brazilian Dental Journal |
| repository.name.fl_str_mv |
Brazilian Dental Journal - Fundação Odontológica de Ribeirão Preto (FUNORP) |
| repository.mail.fl_str_mv |
bdj@forp.usp.br||sergio@fosjc.unesp.br |
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1754204095653085184 |