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Transforming Growth Factor-β1 and Runt-related Transcription Factor 2 as Markers of Osteogenesis in Stem Cells from Human Exfoliated Deciduous Teeth Enriched Bone Grafting

BACKGROUND: Stem cells from human exfoliated deciduous teeth (SHED) are one source of adult stem cells which can proliferate and differentiate into many types of tissues than any other stem cells. SHED represent potential stem cells for therapeutic therapy and tissue engineering. AIMS: The aim of th...

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Autores principales: Prahasanti, Chiquita, Ulfah, Noer, Kusuma, Ivan Indra, Hayati, Nur, Ernawati, Diah Savitri, Krismariono, Agung, Bramantoro, Taufan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868629/
https://www.ncbi.nlm.nih.gov/pubmed/31772465
http://dx.doi.org/10.4103/ccd.ccd_609_18
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author Prahasanti, Chiquita
Ulfah, Noer
Kusuma, Ivan Indra
Hayati, Nur
Ernawati, Diah Savitri
Krismariono, Agung
Bramantoro, Taufan
author_facet Prahasanti, Chiquita
Ulfah, Noer
Kusuma, Ivan Indra
Hayati, Nur
Ernawati, Diah Savitri
Krismariono, Agung
Bramantoro, Taufan
author_sort Prahasanti, Chiquita
collection PubMed
description BACKGROUND: Stem cells from human exfoliated deciduous teeth (SHED) are one source of adult stem cells which can proliferate and differentiate into many types of tissues than any other stem cells. SHED represent potential stem cells for therapeutic therapy and tissue engineering. AIMS: The aim of this study was to compare the expression of transforming growth factor-β1 (TGF-β1) and runt-related transcription factor 2 (RUNX2) in hydroxyapatite (HA) scaffold with SHED. SUBJECTS AND METHODS: Eight experimental animals were divided into two groups. The first group was transplanted with HA and the second with HA and SHED. The expression of TGF-β1 and RUNX2 was seen 21 days later by means of immunohistochemical analysis. STATISTICAL ANALYSIS USED: Data were analyzed using an independent t-test with a significance level of 5%. RESULTS: The analysis results of an independent t-test showed a significant difference between the two groups. The second group given HA with SHED showed a significantly higher expression of TGF-β1 and RUNX2 than that of the first group. CONCLUSIONS: Expression of TGF-β1 and RUNX2 occurs after the application of HA with SHED, while TGF-β1 and RUNX2 expression in the HA with SHED group was significantly higher than in the group without SHED.
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spelling pubmed-68686292019-11-26 Transforming Growth Factor-β1 and Runt-related Transcription Factor 2 as Markers of Osteogenesis in Stem Cells from Human Exfoliated Deciduous Teeth Enriched Bone Grafting Prahasanti, Chiquita Ulfah, Noer Kusuma, Ivan Indra Hayati, Nur Ernawati, Diah Savitri Krismariono, Agung Bramantoro, Taufan Contemp Clin Dent Original Article BACKGROUND: Stem cells from human exfoliated deciduous teeth (SHED) are one source of adult stem cells which can proliferate and differentiate into many types of tissues than any other stem cells. SHED represent potential stem cells for therapeutic therapy and tissue engineering. AIMS: The aim of this study was to compare the expression of transforming growth factor-β1 (TGF-β1) and runt-related transcription factor 2 (RUNX2) in hydroxyapatite (HA) scaffold with SHED. SUBJECTS AND METHODS: Eight experimental animals were divided into two groups. The first group was transplanted with HA and the second with HA and SHED. The expression of TGF-β1 and RUNX2 was seen 21 days later by means of immunohistochemical analysis. STATISTICAL ANALYSIS USED: Data were analyzed using an independent t-test with a significance level of 5%. RESULTS: The analysis results of an independent t-test showed a significant difference between the two groups. The second group given HA with SHED showed a significantly higher expression of TGF-β1 and RUNX2 than that of the first group. CONCLUSIONS: Expression of TGF-β1 and RUNX2 occurs after the application of HA with SHED, while TGF-β1 and RUNX2 expression in the HA with SHED group was significantly higher than in the group without SHED. Wolters Kluwer - Medknow 2018 /pmc/articles/PMC6868629/ /pubmed/31772465 http://dx.doi.org/10.4103/ccd.ccd_609_18 Text en Copyright: © 2019 Contemporary Clinical Dentistry http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Prahasanti, Chiquita
Ulfah, Noer
Kusuma, Ivan Indra
Hayati, Nur
Ernawati, Diah Savitri
Krismariono, Agung
Bramantoro, Taufan
Transforming Growth Factor-β1 and Runt-related Transcription Factor 2 as Markers of Osteogenesis in Stem Cells from Human Exfoliated Deciduous Teeth Enriched Bone Grafting
title Transforming Growth Factor-β1 and Runt-related Transcription Factor 2 as Markers of Osteogenesis in Stem Cells from Human Exfoliated Deciduous Teeth Enriched Bone Grafting
title_full Transforming Growth Factor-β1 and Runt-related Transcription Factor 2 as Markers of Osteogenesis in Stem Cells from Human Exfoliated Deciduous Teeth Enriched Bone Grafting
title_fullStr Transforming Growth Factor-β1 and Runt-related Transcription Factor 2 as Markers of Osteogenesis in Stem Cells from Human Exfoliated Deciduous Teeth Enriched Bone Grafting
title_full_unstemmed Transforming Growth Factor-β1 and Runt-related Transcription Factor 2 as Markers of Osteogenesis in Stem Cells from Human Exfoliated Deciduous Teeth Enriched Bone Grafting
title_short Transforming Growth Factor-β1 and Runt-related Transcription Factor 2 as Markers of Osteogenesis in Stem Cells from Human Exfoliated Deciduous Teeth Enriched Bone Grafting
title_sort transforming growth factor-β1 and runt-related transcription factor 2 as markers of osteogenesis in stem cells from human exfoliated deciduous teeth enriched bone grafting
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868629/
https://www.ncbi.nlm.nih.gov/pubmed/31772465
http://dx.doi.org/10.4103/ccd.ccd_609_18
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