口腔扁平苔藓患者血清差异蛋白表达检测及意义

目的探讨口腔扁平苔藓（OLP）患者血清差异蛋白表达及意义。方法选择6例OLP患者（观察组）和6例健康志愿者（对照组）,抽取空腹静脉血后采用苯酚抽提法提取血清蛋白,Bradford法测定蛋白含量,双向荧光差异凝胶电泳法分离检测差异蛋白点,液相色谱-质谱联用技术鉴定差异蛋白。选择其中研究较少的蛋白,采用Western blotting法检测两组蛋白相对表达量。结果两组血清差异蛋白点（583±183）个,其中重复性好的蛋白差异点20个,质谱分析蛋白序列鉴定出12种蛋白质。12种蛋白质中,7种（补体C3、激肽原、α-2-巨球蛋白、人抗凝血酶Ⅲ、分泌型Ig A、补体C9、β-1-金属结合球蛋白）在观察组...

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Bibliographic Details
Published in山东医药 Vol. 56; no. 16; pp. 11 - 14
Main Author 刘健 刘铁军 安欣 李昆珊 贾楠 许彦枝
Format Magazine Article
LanguageChinese
Published 河北医科大学第四医院,石家庄,050011 2016
Subjects
人抗凝血酶
双向荧光差异凝胶电泳
口腔扁平苔藓
蛋白质组
补体C3
载脂蛋白A
双向荧光差异凝胶电泳
补体C3
proteomics
载脂蛋白A
human antithrombin
serum com-plement C3
蛋白质组
oral lichen planus
apolipoprotein A
人抗凝血酶
口腔扁平苔藓
two-dimensional fluorescence difference gel electrophoresis
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ISSN1002-266X
DOI10.3969/j.issn.1002-266X.2016.16.004

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Summary:目的探讨口腔扁平苔藓（OLP）患者血清差异蛋白表达及意义。方法选择6例OLP患者（观察组）和6例健康志愿者（对照组）,抽取空腹静脉血后采用苯酚抽提法提取血清蛋白,Bradford法测定蛋白含量,双向荧光差异凝胶电泳法分离检测差异蛋白点,液相色谱-质谱联用技术鉴定差异蛋白。选择其中研究较少的蛋白,采用Western blotting法检测两组蛋白相对表达量。结果两组血清差异蛋白点（583±183）个,其中重复性好的蛋白差异点20个,质谱分析蛋白序列鉴定出12种蛋白质。12种蛋白质中,7种（补体C3、激肽原、α-2-巨球蛋白、人抗凝血酶Ⅲ、分泌型Ig A、补体C9、β-1-金属结合球蛋白）在观察组血清中表达降低,5种（结合珠蛋白、铜蓝蛋白、载脂蛋白AⅠ、维生素D、人类因子B）表达升高。观察组血清补体C3和人抗凝血酶Ⅲ蛋白相对表达量均低于对照组,载脂蛋白AⅠ高于对照组（P均〈0.01）。结论 OLP患者血清中存在12种差异蛋白质,血清补体C3和人抗凝血酶Ⅲ蛋白表达均降低,载脂蛋白AⅠ表达升高,其发病可能与免疫功能降低及感染有关。
Bibliography:LIU Jian, LIU Tiejun, AN Xin, LI Kunshan, JIA Nan, XU Yanzhi （The Forth Hospital of Hebei Medical University, Shijiazhuang 050011, China）
37-1156/R
oral lichen planus; two-dimensional fluorescence difference gel electrophoresis; proteomics; serum complement C3; apolipoprotein AⅠ; human antithrombin
Objective To detect the differentially expressed serum proteins in patients with oral lichen planus（ OLP）and explore their significance. Methods Six OLP patients（ observation group） and the matched health adults（ control group） were selected and we drew their venous blood. Serum proteins were extracted by phenol extraction. The protein concentration was determined by Bradford method. Serum proteins were separated by two-dimensional fluorescence difference gel electrophoresis（ 2-D DIGE）,the differential proteins were identified by mess spectrometry and the expression of the proteins was detected by Western blotting in the two groups. Results In average,the number of differential protein spots was（ 583± 183）,during whic
ISSN:1002-266X
DOI:10.3969/j.issn.1002-266X.2016.16.004