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作 者:付嘉[1] 方艳秋[1] 徐立[1] 李明辉[1] 刘桂英[1] 姜艳芳[1] 段秀梅[1] 刘力华[1] 许淑芬[1] 谭岩[1]
机构地区:[1]吉林大学第一医院中心实验室,吉林长春130021
出 处:《吉林大学学报(医学版)》2006年第4期654-657,共4页Journal of Jilin University:Medicine Edition
基 金:教育部高等学校博士学科点专项基金资助课题(20040183066);吉林省科技厅资助课题(20030419);吉林省杰出青年基金资助课题(20050113);吉林大学青年基金资助课题(2005年)
摘 要:目的:探讨重组人β2糖蛋白1(hrβ2-GP1)对抗磷脂抗体综合征(APS)患者血清诱导内皮细胞系产生细胞间黏附分子-1(ICAM-1)的影响。方法:应用pQE30表达载体表达hrβ2-GP1,Western blotting对重组蛋白进行鉴定;应用hrβ2-GP1处理前后的APS患者血清分别与内皮细胞株EA.hy926共孵育,细胞ELISA和RT-PCR方法分析处理前后EA.hy926表达ICAM-1的变化。结果:成功构建pQE30-hβ2-GP1,并对表达产物进行了纯化和鉴定,所获得的蛋白与预期的大小一致,并具有人β2-GP1的抗原性;rhβ2-GP1处理后的APS患者血清与处理前比较,与其孵育的内皮细胞系EA.hy926表达ICAM-1在蛋白和mRNA水平均明显降低,这种抑制作用随着rhβ2-GP1的浓度增加而逐渐增强。结论:抗β2糖蛋白1抗体(anti-β2GP1)促进内皮细胞系EA.hy926表达ICAM-1,hrβ2-GP1可中和此作用。Objectivo To investigate the effect of human recombinant β2-glycoprotein-1 (hrβ2-GP1) on expression of intercellular adhesion molecular-1 (ICAM-1) in endothelial cell line induced by plasma from anti-phospholipid antibody syndrome (APS) patients. Methods hrβ2-GP1 was expressed using pQE30 expression vector and characterized by Western blotting, hrβ2-GP1 treated and untreated plasma from APS patients were incubated with endothilial cell line EA. hy 926. The changes of ICAM-1 expressed by EA. hy 926 were analyzed using cell-ELISA and RT-PCR. Results PQE30-hβ2-GP1 was constructed, the exprssion products were purified and characterized. Compared with the untreated one, the membranous protein and mRNA expression of ICAM-1 in EA. hy926 of the hrβ2-GP1 treated plasma from APS patients were significantly decreased. Conclusion Anti-β2-GP1 antibody can elevate the expression of ICAM-1 in endothelial cell line EA. hy926, hrβ2-GP1 can neutralize this effect.
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