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2,3,5,4'-Tetrahydroxystilbene-2-O-ß-glucoside potentiates self-renewal of human dental pulp stem cells via the AMPK/ERK/SIRT1 axis.
Lin, C-Y; Chin, Y-T; Kuo, P-J; Lee, H-W; Huang, H-M; Lin, H-Y; Weng, I-T; Hsiung, C-N; Chan, Y-H; Lee, S-Y.
Afiliação
  • Lin CY; School of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan.
  • Chin YT; Research Center of Tooth Bank and Dental Stem Cell Technology, Taipei Medical University, Taipei, Taiwan.
  • Kuo PJ; Taipei Cancer Center, Taipei Medical University, Taipei, Taiwan.
  • Lee HW; PhD Program for Cancer Biology and Drug Discovery College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.
  • Huang HM; Department of Periodontology School of Dentistry, National Defense Medical Center and Tri-Service General Hospital, Taipei, Taiwan.
  • Lin HY; Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei, Taiwan.
  • Weng IT; Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Hsiung CN; School of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan.
  • Chan YH; Taipei Cancer Center, Taipei Medical University, Taipei, Taiwan.
  • Lee SY; PhD Program for Cancer Biology and Drug Discovery College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.
Int Endod J ; 51(10): 1159-1170, 2018 Oct.
Article em En | MEDLINE | ID: mdl-29635697
ABSTRACT

AIM:

To evaluate the effect of 2,3,5,4'-tetrahydroxystilbene-2-O-ß-D-glucoside (THSG) on cell proliferation and examine the mechanisms of THSG-enhanced proliferative potential in human dental pulp stem cells (hDPSC).

METHODOLOGY:

After treatment with THSG, hDPSC were collected. Cell viability was determined by MTS assay, while messenger RNA (mRNA) expressions of proliferation and stem cell markers were analyzed using real-time PCR. Flow cytometry was also conducted to analysis protein expression of stem cell markers. A colony-forming unit assay of hDPSC was carried out. Cellular telomerase activity was also identified using real-time PCR. In addition, proliferation-related proteins involved in the effects of THSG on hDPSC were analyzed by Western blotting. Data were analyzed using one-way analysis of variance and two-tailed Student's t-test.

RESULTS:

Cell viability, colony-forming rates and telomerase activities of hDPSCs were enhanced after THSG treatment. mRNA expressions of proliferation markers (including expressions of NAD+-dependent histone deacetylase sirtuin 1 (SIRT1), proliferating cell nuclear antigen (PCNA), cyclin D1 and ribonucleotide reductase subunit M2 (RRM2)) increased significantly after THSG treatment (P < 0.05). Treatment with THSG for 3 h significantly augmented SIRT1 protein expression (P < 0.05). Furthermore, activities of proliferation-related proteins (including AMP-activated protein kinase (AMPK) and extracellular signal-regulated kinase (ERK) had also significantly increased at 3 h (P < 0.05). After THSG treatment, increased gene and protein expressions of pluripotent-like stem cell markers (including NANOG, OCT4, and SOX2) were observed.

CONCLUSIONS:

2,3,5,4'-Tetrahydroxystilbene-2-O-ß-glucoside treatment enhanced the renewal ability and proliferative potential of hDPSCs via the AMPK/ERK/SIRT1 axis, which may provide a novel autogenic cell-based therapeutic strategy in regenerative dentistry.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco / Estilbenos / Polpa Dentária / Glucosídeos Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco / Estilbenos / Polpa Dentária / Glucosídeos Idioma: En Ano de publicação: 2018 Tipo de documento: Article