Luo Xiao-yun, Wu Qing-hua, Chen Zhong, Ma Jun, Han Yan-min, Tang Xiao-bin, Wu Zhang-min, Kou Lei, Liu Hui, Li Qing, Jia Yun-feng, Zhang Zhen, He Nan
Department of Vascular Surgery, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Zhonghua Yi Xue Za Zhi. 2010 Jan 19;90(3):157-60.
To investigate differential expression of plasma proteins of patients with Takayasu's arteritis to screen disease-related or phase-related proteins or biomarkers.
From March, 2005 to January, 2006, Plasma of 20 patients with acute Takayasu's arteritis, 20 patients with chronic Takayasu's arteritis, and 20 healthy people as control were collected. Plasma proteins were profiled by two-dimensional electrophoresis. Spots of differential expression were screened by computerized map analysis and identified by matrix assisted laser desorption/ionization time of flight-mass spectrometry. Circulation levels of parts of differential expression proteins were investigated by Elisa in each subject.
Fourteen differential expression proteins were identified, including serum amyloid A, serum amyloid P, fibrinogen, complement C3c, C7, C4 binding protein, factor H related protein-1, immunoglobin, alpha-acid glycoprotein, RAG1 protein, alpha1-microglobin, apolipoprotein A-I, A-IV, transthyretin, haptoglobin. Proteins related to acute and chronic phase were serum amyloid A, fibrinogen, transthyretin, haptoglobin; Circulation levels of Serum amyloid A (SAA) and Complement C4 binding protein (C4BP) were significantly increased in active TA patients comparing to that in inactive TA patients and in controls (SAA: 95.9 vs 49.2, P = 0.009 and 23.9 mg/L, P = 0.001, respectively; C4BP: 88.5 vs 61.7, P = 0.023 and 32.6 mg/L, P < 0.001, respectively).
Acute phase proteins and immune proteins may possible be markers for diagnosis and activity of Takayasu's arteritis, Complement activity, complement modulation protein and antibody production may be involved in immune mechanism of Takayasu's arteritis. Further study of these proteins may be helpful to elucidate the pathologic mechanism of Takayasu's arteritis.
研究大动脉炎患者血浆蛋白的差异表达,以筛选疾病相关或阶段相关的蛋白或生物标志物。
2005年3月至2006年1月,收集20例急性大动脉炎患者、20例慢性大动脉炎患者的血浆,以及20例健康人的血浆作为对照。采用二维电泳对血浆蛋白进行分析。通过计算机图谱分析筛选差异表达斑点,并采用基质辅助激光解吸/电离飞行时间质谱进行鉴定。采用酶联免疫吸附测定法检测各研究对象中部分差异表达蛋白的循环水平。
共鉴定出14种差异表达蛋白,包括血清淀粉样蛋白A、血清淀粉样蛋白P、纤维蛋白原、补体C3c、C7、C4结合蛋白、H因子相关蛋白-1、免疫球蛋白、α-酸性糖蛋白、重组激活基因1蛋白、α1-微球蛋白、载脂蛋白A-I、A-IV、转甲状腺素蛋白、触珠蛋白。与急慢性期相关的蛋白有血清淀粉样蛋白A、纤维蛋白原、转甲状腺素蛋白、触珠蛋白;与静止期大动脉炎患者及健康对照组相比,活动期大动脉炎患者血清淀粉样蛋白A(SAA)和补体C4结合蛋白(C4BP)的循环水平显著升高(SAA:分别为95.9 vs 49.2,P = 0.009和23.9 mg/L,P = 0.001;C4BP:分别为88.5 vs 61.7,P = 0.023和32.6 mg/L,P < 0.001)。
急性期蛋白和免疫蛋白可能是大动脉炎诊断及活动度的标志物,补体活性、补体调节蛋白及抗体产生可能参与了大动脉炎的免疫机制。对这些蛋白的进一步研究可能有助于阐明大动脉炎的病理机制。