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[Effect of Regulating A20 Expression on NF-κB Expression and Biological Characteristics of Jurkat Cells].
Wang, Zhe; Xiao, Shi-Shan; Ding, Qian; Wang, Qing; Zhou, Sheng-Nan; Li, Zhe; Zhu, Hong-Qian.
Afiliação
  • Wang Z; Department of Hematology, Guizhou Provincial People's Hospital, Guiyang 550002, Guizhou Province, China.
  • Xiao SS; Department of Hematology, Guizhou Provincial People's Hospital, Guiyang 550002, Guizhou Province, China.
  • Ding Q; Department of Hematology, Guizhou Provincial People's Hospital, Guiyang 550002, Guizhou Province, China.
  • Wang Q; Department of Hematology, Guizhou Provincial People's Hospital, Guiyang 550002, Guizhou Province, China.
  • Zhou SN; Department of Hematology, Guizhou Provincial People's Hospital, Guiyang 550002, Guizhou Province, China.
  • Li Z; Department of Hematology, Guizhou Provincial People's Hospital, Guiyang 550002, Guizhou Province, China.
  • Zhu HQ; Department of Hematology, Guizhou Provincial People's Hospital, Guiyang 550002, Guizhou Province, China,E-mail: zhuhongqian@126.com.
Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 28(4): 1144-1151, 2020 Aug.
Article em Zh | MEDLINE | ID: mdl-32798389
OBJECTIVE: To explore the effect of regulating A20 expression on NF-κB and biological characteristics of Jurkat cells with glucocorticoid (GC) resistance. METHODS: CCRF CEM and Jurkat cells were treated with dexamethasone (DEX) at concentrations of 100、10、1、0.1、0.01 and 0.001 µmol/L, and cultured for 24、48 and 72 h. The proliferation inhibition rate of Jurkat cell was detected by CCK-8. A20 plasmid was constructed, A20-siRNA was designed and synthesized, and transfected into Jurkat cells by liposome. CCK-8 was used to detect the proliferation rates of Jurkat cells in different concentrations of DEX group, DEX combined with A20 plasmid group and A20-siRNA group. The mRNA expression level of NF-κB was detected by RT-qPCR, the protein expression level of NF-κB was detected by Western blot, and the apoptosis of Jurkat cells was examined by flow cytometry. RESULTS: The inhibitory effects of DEX at different concentrations on the growth of CCRF CEM cells were time-dependent (r=0.984, P<0.05) and concentration-dependent (r=0.966, P<0.05). At the point of 24 hour, the IC50 approached 1 µmol/L in CCRF CEM cells. Great large differences began to appear between 1 and 10 µmol/L, the proliferation rate of Jurkat cells treated with 1 µmol/L DEX did not show a significant change. Therefore, 1 µmol/L was selected as control group. The cell proliferation rate of A20 plasmid transfection combined with different concentrations of DEX group was lower than that of DEX group and A20-siRNA combined with DEX group. After transfection of A20 plasmid, the expression level of NF-κB was significantly lower than that of control group (P<0.05), and the apoptotic rate was significantly higher than that of control group (P<0.05). After transfection of Jurkat cells with A20-siRNA, the expression level of NF-κB was significantly higher than that of control group (P<0.05). The apoptotic rate of cells in A20-siRNA group was not significantly changed (P>0.05). CONCLUSION: Jurkat cells are resistant to DEX. A20 overexpression combined with DEX can increase sensitivity of Jurkat cells with GC resistance and decrease the proliferation rate of Jurkat cells, down-regulate the expression level of NF-κB and promote the apoptosis of Jurkat cells.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: NF-kappa B / Apoptose Idioma: Zh Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: NF-kappa B / Apoptose Idioma: Zh Ano de publicação: 2020 Tipo de documento: Article