The expression profile of dental pulp-derived stromal cells supports their limited capacity to differentiate into adipogenic cells

Letícia Fracaro, Alexandra C. Senegaglia, Roberto H. Herai, Amanda Leitolis, Lidiane M. Boldrini-Leite, Carmen L. K. Rebelatto, Paul J. Travers, Paulo R. S. Brofman, Alejandro Correa

Research output: Contribution to journalArticlepeer-review

Abstract

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.
Original languageEnglish
JournalInternational Journal of Molecular Sciences
Volume21
Issue number8
DOIs
Publication statusPublished - 15 Apr 2020

Keywords / Materials (for Non-textual outputs)

  • adipogenesis
  • ADSCs
  • DPSCs
  • transcription profile
  • WNT/BMP pathways

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