IL-2诱导类风湿关节炎与骨关节炎T淋巴细胞STAT3 STAT5酪氨酸磷酸化状态的比较  被引量:1

Comparison of the status of STAT3 and STAT5 tyrosine phosphorylation in T-lymphocytes induced by IL-2 between rheumatoid arthritis and osteoarthritis

在线阅读下载全文

作  者:熊奡[1] 吕厚山[1] 孙铁铮[1] 陈占昆[1] 蒋东芳[1] 姜军[1] 

机构地区:[1]北京大学人民医院关节病诊疗中心,100044

出  处:《中华风湿病学杂志》2005年第10期590-593,共4页Chinese Journal of Rheumatology

基  金:北京大学211重点学科基金资助项目(904)

摘  要:目的观察白细胞介素(IL)-2作用于类风湿关节炎(RA)与骨关节炎(OA)外周血T淋巴细胞前后,T淋巴细胞中STAT3及STAT5的酪氨酸磷酸化活化状态,并进行比较。方法从RA与OA患者的外周血中分离培养单个核细胞,继而纯化得到T淋巴细胞,静息后,用重组人IL-2刺激,在各时相裂解细胞,收获提取蛋白,进行Westernblot分析。结果在静息后,RA与OA的外周血T淋巴细胞中STAT3与STAT5均处于极低水平磷酸化的状态;在IL-2作用后,T淋巴细胞中STAT3和STAT5发生时相性的酪氨酸磷酸化,而RA的T淋巴细胞磷酸化程度较OA显著增高。结论IL-2对RA患者T淋巴细胞的STAT3和STAT5过度激活,引起T淋巴细胞中IL-2信号传导的异常放大效应,可能在RA的发病过程中发挥重要作用。Objective To compare tyrosine phosphorylation of STAT3 and STAT5 induced by IL-2 in T-lymphocytes from peripheral blood of patients with rheumatoid arthritis (RA) and osteoarthritis (OA). Methods Peripheral blood mononuclear cells (PBMCs) were isolated from RA and OA patients, then T-lymphocytes purified from PBMCs were stimulated by rhlL-2. Total proteins of T cells were extracted after different time intervals. Results After rest, the tyrosine phosphorylation of STAT3 and STATS in T-lymphocytes from both RA and OA patients were at extremely low level. After stimulated with IL-2, tyrosine phosphorylation of both STAT3 and STAT5 in T cells from RA were time dependent and the phosphorylation was prominent than that from OA. Conclusion Even in RA, STAT3 and STAT5 pathway in T-lymphocytes from peripheral blood can not he automatically activated. The excessive tyrosine phosphorylation of STAT3 and STATS in RAT cells probably amplify the downstream signal transduction of IL-2, thus lead to an enhancement of transcription of certain genes, which seem to play some important roles in the pathogenesis of RA.

关 键 词:关节炎 类风湿 T淋巴细胞 白细胞介素2 信号转导子和转录激活子 外周血T淋巴细胞 重组人IL-2 酪氨酸磷酸化 STAT3 类风湿关节炎 STAT5 

分 类 号:R593.22[医药卫生—内科学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象