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The Expression Profile of Dental Pulp-Derived Stromal Cells Supports Their Limited Capacity to Differentiate into Adipogenic Cells
Mesenchymal stromal cells (MSCs) can self-renew, differentiate into specialised cells and have different embryonic origins—ectodermal for dental pulp-derived MSCs (DPSCs) and mesodermal for adipose tissue-derived MSCs (ADSCs). Data on DPSCs adipogenic differentiation potential and timing vary, and t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215853/ https://www.ncbi.nlm.nih.gov/pubmed/32326648 http://dx.doi.org/10.3390/ijms21082753 |
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author | Fracaro, Letícia Senegaglia, Alexandra C. Herai, Roberto H. Leitolis, Amanda Boldrini-Leite, Lidiane M. Rebelatto, Carmen L. K. Travers, Paul J. Brofman, Paulo R. S. Correa, Alejandro |
author_facet | Fracaro, Letícia Senegaglia, Alexandra C. Herai, Roberto H. Leitolis, Amanda Boldrini-Leite, Lidiane M. Rebelatto, Carmen L. K. Travers, Paul J. Brofman, Paulo R. S. Correa, Alejandro |
author_sort | Fracaro, Letícia |
collection | PubMed |
description | Mesenchymal stromal cells (MSCs) can self-renew, differentiate into specialised cells and have different embryonic origins—ectodermal for dental pulp-derived MSCs (DPSCs) and mesodermal for adipose tissue-derived MSCs (ADSCs). Data on DPSCs adipogenic differentiation potential and timing vary, and the lack of molecular and genetic information prompted us to gain a better understanding of DPSCs adipogenic differentiation potential and gene expression profile. While DPSCs differentiated readily along osteogenic and chondrogenic pathways, after 21 days in two different types of adipogenic induction media, DPSCs cultures did not contain lipid vacuoles and had low expression levels of the adipogenic genes proliferator-activated receptor gamma (PPARG), lipoprotein lipase (LPL) and CCAAT/enhancer-binding protein alpha (CEBPA). To better understand this limitation in adipogenesis, transcriptome analysis in undifferentiated DPSCs was carried out, with the ADSC transcriptome used as a positive control. In total, 14,871 transcripts were common to DPSCs and ADSCs, some were unique (DPSCs: 471, ADSCs: 1032), and 510 were differentially expressed genes. Detailed analyses of overrepresented transcripts showed that DPSCs express genes that inhibit adipogenic differentiation, revealing the possible mechanism for their limited adipogenesis. |
format | Online Article Text |
id | pubmed-7215853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72158532020-05-22 The Expression Profile of Dental Pulp-Derived Stromal Cells Supports Their Limited Capacity to Differentiate into Adipogenic Cells Fracaro, Letícia Senegaglia, Alexandra C. Herai, Roberto H. Leitolis, Amanda Boldrini-Leite, Lidiane M. Rebelatto, Carmen L. K. Travers, Paul J. Brofman, Paulo R. S. Correa, Alejandro Int J Mol Sci Article Mesenchymal stromal cells (MSCs) can self-renew, differentiate into specialised cells and have different embryonic origins—ectodermal for dental pulp-derived MSCs (DPSCs) and mesodermal for adipose tissue-derived MSCs (ADSCs). Data on DPSCs adipogenic differentiation potential and timing vary, and the lack of molecular and genetic information prompted us to gain a better understanding of DPSCs adipogenic differentiation potential and gene expression profile. While DPSCs differentiated readily along osteogenic and chondrogenic pathways, after 21 days in two different types of adipogenic induction media, DPSCs cultures did not contain lipid vacuoles and had low expression levels of the adipogenic genes proliferator-activated receptor gamma (PPARG), lipoprotein lipase (LPL) and CCAAT/enhancer-binding protein alpha (CEBPA). To better understand this limitation in adipogenesis, transcriptome analysis in undifferentiated DPSCs was carried out, with the ADSC transcriptome used as a positive control. In total, 14,871 transcripts were common to DPSCs and ADSCs, some were unique (DPSCs: 471, ADSCs: 1032), and 510 were differentially expressed genes. Detailed analyses of overrepresented transcripts showed that DPSCs express genes that inhibit adipogenic differentiation, revealing the possible mechanism for their limited adipogenesis. MDPI 2020-04-15 /pmc/articles/PMC7215853/ /pubmed/32326648 http://dx.doi.org/10.3390/ijms21082753 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Fracaro, Letícia Senegaglia, Alexandra C. Herai, Roberto H. Leitolis, Amanda Boldrini-Leite, Lidiane M. Rebelatto, Carmen L. K. Travers, Paul J. Brofman, Paulo R. S. Correa, Alejandro The Expression Profile of Dental Pulp-Derived Stromal Cells Supports Their Limited Capacity to Differentiate into Adipogenic Cells |
title | The Expression Profile of Dental Pulp-Derived Stromal Cells Supports Their Limited Capacity to Differentiate into Adipogenic Cells |
title_full | The Expression Profile of Dental Pulp-Derived Stromal Cells Supports Their Limited Capacity to Differentiate into Adipogenic Cells |
title_fullStr | The Expression Profile of Dental Pulp-Derived Stromal Cells Supports Their Limited Capacity to Differentiate into Adipogenic Cells |
title_full_unstemmed | The Expression Profile of Dental Pulp-Derived Stromal Cells Supports Their Limited Capacity to Differentiate into Adipogenic Cells |
title_short | The Expression Profile of Dental Pulp-Derived Stromal Cells Supports Their Limited Capacity to Differentiate into Adipogenic Cells |
title_sort | expression profile of dental pulp-derived stromal cells supports their limited capacity to differentiate into adipogenic cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215853/ https://www.ncbi.nlm.nih.gov/pubmed/32326648 http://dx.doi.org/10.3390/ijms21082753 |
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