Akt pathway and its regulatory mechanism in the peripheral blood mononuclear cells in patients with systemic lupus erythematosus
10.3760/cma.j.issn.1007-7480.2016.06.003
- VernacularTitle:蛋白激酶B通路在系统性红斑狼疮患者外周血单个核细胞凋亡中的作用及其调控机制
- Author:
Dongyu CHEN
;
Fang LI
;
Guangting ZHU
- Publication Type:Journal Article
- Keywords:
Lupus erythematosus,systemic;
Akt;
Peripheral blood mononuclear cell;
Apoptosis
- From:
Chinese Journal of Rheumatology
2016;20(6):368-371
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the expression of Akt in peripheral blood mononuclear cells (PBMCs) and its regulatory role on its downstream molecules forkhead box transcription factor O1 (FOXO1) and Bim in patients with systemic lupus erythematosus (SLE).The role of Akt/FOXO1/Bim signaling pathway on PBMCs apoptosis was clarified.Methods Sixty-three SLE patients and 23 healthy controls were enrolled.PBMC were separated from the peripheral blood specimen.Western blot technique was applied to analyze the expression of Akt,FOXO1 and Bim.Flow cytometry was applied to analyze PBMCs apoptosis.The t-test was used for statistical analysis.Results The apoptosis of PBMCs in patients with active SLE [(16.3±4.0)％] was significantly higher than that of patients with inactive SLE [(5.6 ±2.9)％] and normal controls [(5.2 ±4.2)％,t=4.83,5.05;P＜0.05].The levels of phosphorylation of Akt,FOXO1 and Bim expression was significantly decreased in patients with active SLE as compared with controls and patients with inactive SLE (P＜0.05).However,these indicators had no significant difference between the controls and patients with inactive SLE (P＞0.05).Conclusion ① The results of this study suggest that the expression level of Akt may be a good indicator for disease activity of SLE.Decrease of Akt may promote the occurrence and development of SLE.② Akt activity decline may lead to increased apoptosis of PBMCs.In this process,Akt may regulate its downstream FOXO1 and Bim phosphorylation levels which can enhance their ability to pro-apoptotic.
