STAT蛋白                        
                
                                
                        
                            贾纳斯激酶                        
                
                                
                        
                            车站3                        
                
                                
                        
                            细胞凋亡                        
                
                                
                        
                            Janus激酶2                        
                
                                
                        
                            分子生物学                        
                
                                
                        
                            细胞周期蛋白D1                        
                
                                
                        
                            信号转导                        
                
                                
                        
                            细胞周期                        
                
                                
                        
                            化学                        
                
                                
                        
                            STAT1                        
                
                                
                        
                            癌症研究                        
                
                                
                        
                            生物                        
                
                                
                        
                            生物化学                        
                
                        
                    
            作者
            
                Yongsheng Yang,Qiumei Dong,Chunjie Ma,Yongle Li,Kun Chen,Suo Zhang,Yudi Zhang            
         
                    
            出处
            
                                    期刊:Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan
                                                                        日期:2019-04-01
                                                        卷期号:39 (2): 181-190
                                                        被引量:4
                                
         
        
    
            
        
                
            摘要
            
            Objective To investigate the efficacy of Zhonglun'a-decoction-containing serum (ZHONGL-CS) on the in vitro apoptosis of fibroblast-like synoviocytes (FLS) from rats with collagen-induced arthritis (CIA) by investigating the Janus kinase/signal transducer and activator of transcription (JAK/STAT) signaling pathway. Methods A CIA rat model was established using bovine type Ⅱ collagen. FLS were isolated, cultured and identified. A cell counting kit-8 was used to detect cell activity. The half maximal inhibitory concentration (IC50) was calculated. Experimental subjects were divided into control, CIA, ZHONGL-CS, JAK2 inhibitor AG490, and ZHONGLCS with AG490 groups. The in vitro cell cycle and apoptosis rate were detected in FLS by flow cytometry. Bcl-2-associated X protein (Bax), B-cell lymphoma 2 (Bcl-2), caspase-3, cyclin D1, phosphorylated JAK2, STAT1, and STAT3 protein expressions in FLS were examined by Western blotting. JAK2, STAT1 and STAT3 mRNA levels were examined by quantitative real-time polymerase chain reaction. Results Compared with the CIA group, FLS proliferation was inhibited, the FLS G0/G1 cell cycle was arrested, and the rate of FLS apoptosis was increased in the ZHONGL-CS group. In the ZHONGLCS group, the protein levels of Bcl-2 and cyclin D1 were reduced compared with the CIA group and the levels of Bax and caspase-3 in FLS were increased. In the ZHONGL-CS group, the expressions of JAK2, STAT1, and STAT3 mRNA and the levels of phosphorylated JAK2, STAT1, and STAT3 proteins were reduced. Conclusion ZHONGL-CS may induce FLS apoptosis in CIA rats. Activation of the JAK/STAT signaling pathway was inhibited in FLS in vitro.
         
            
 
                 
                
                    
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