Acta Anatomica Sinica ›› 2022, Vol. 53 ›› Issue (1): 66-74.doi: 10.16098/j.issn.0529-1356.2022.01.009

• Cancer Biology • Previous Articles     Next Articles

Effect of tumor necrosis factorα overexpress on the biological properties dental pulp stem cells in microoxidative stress

LI Wei YANG Gan-un PENG Jian-an2  HU Hong-mei2* ZHOU Xing-chen1    

  1. 1.Oral Department of Medical College, Jinggangshan University; 2.Department of Histology and Anatomy of  Medical college,Jinggangshan University, Jiangxi Ji’an 343000, China
  • Received:2020-11-08 Revised:2021-01-06 Online:2022-02-06 Published:2022-02-06
  • Contact: HU Hong-mei E-mail:liwei8503@126.com

Abstract:

Objective  To investigate the effect of tumor necrosis factor-α(TNF-α) on biological properties of dental pulp stem cells (DPSCs) in low-oxidation stress.    Methods  The experimental groups were as follows: normox, normox control plasmid, normox-TNF-α, 3% O2, control plasmid-3% O2、TNF-α-3% O2.DPSCs were resuscitated and cultured firstly, then lentivirus TNF-α transfected cells were cultured in a CO2 incubator at 37 ℃. The expression of TNF-α  was detected by ELISA in each group, and the expression of TNF-α under oxidative stress was detected by RT-PCR,the expressions of alkaline phosphatase(ALP) and dentin sialophosphoprotein(DSPP) were detected by Real-time PCR and Western blotting,the proliferation of DPSCs cells transfected with TNF-α was detected by flow cytometry and MTT.    Results  After lentivirus-TNF-α transfected cells for 10 hours, the green fluorescence signal could be observed under inverted fluorescence microscope, TNF-α overexpression could enhance the proliferation of DSPP in hypoxic environment,and hypoxia microenvironment can greatly increase the expression of TNF-α, Western blotting and Real-time PCR showed that there were significant differences in the expression of ALP and DSPP in DPSCs(P<0.05).    Conclusion  TNF-α overexpression can improve the proliferation efficiency and differentiation efficiency of DPSCs in hypoxic microenvironment. 

Key words: Micro oxidation, Tumor necrosis factor-α, Dental pulp stem cells, Western blotting, Human

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