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Chinese Journal of Stomatological Research(Electronic Edition) ›› 2011, Vol. 5 ›› Issue (04): 347-355. doi: 10.3877/cma.j.issn.1674-1366.2011.03.003

• Original Articles • Previous Articles    

Transient transfection of transcription factor Oct4 on the expressions of pluripotencyassociated genes in human dental pulp cells

Xi WEI1,(), Fang ZHANG1, Lu LIU1, Xiaoyan ZHOU1, Qian-ying KONG1   

  1. 1.Guanghua School of Stomatology, Institute of Stomatological Research,Sun Yat-sen University, Guangzhou 510055, China
  • Received:2011-01-14 Online:2011-08-01 Published:2025-02-24
  • Contact: Xi WEI

Abstract:

Objective

To investigate the effect of Ad5-Oct4-EGFP transfection on the pluripotency-associated genes expressions of human dental pulp cells (DPCs).

Methods

The recombinant adenovirus was constructed by Admax system, which carried transcription factor Oct4 and enhanced green fluorescence protein (EGFP). After transfected with different multiplicities of infection (MOI) for 48 hours, the transfection efficiency was calculated under fluorescence microscope and optimal MOI was selected for this Ad5-Oct4-EGFP transfer. The mRNA expressions of Oct4 AP Nanog Utf1 Sox2 were detected in the transfected cells at days 1, 2, 3, 5,7 and 14 by RT-PCR.

Results

The recombinant adenoviral vector of Oct4 gene was successfully constructed and high titer of the recombinant adenovirus was obtained. The MOI value of 200 was selected as the optimal MOI for the further study. The mRNA levels of Oct4 Utf1 Nanog AP were expressed at day 1 in Ad5-Oct4-EGFP transfected group, reaching the peak value at day 7 (P <0.05) and then decreased along time. AP mRNA level was significantly greater than Oct4 Utf1 and Nanog at day 7 (P <0.05). Expression of Sox2 mRNA were not detected.

Conclusions

Our study has demonstrated that Oct4 can activate the key pluripotency-associated genes in DPCs and may influence their developmental potency.

Key words: Dental pulp cells, Transcription factor Oct4, Pluripotency-associated genes

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