国际麻醉学与复苏杂志   2017, Issue (11): 10-10
    
不均一性核糖核蛋白A2/B1在脂多糖诱导的血管内皮细胞通透性增加中的作用
王雷, 陈依, 朱科明1()
1.第二军医大学长海医院麻醉科
Effect of heterogeneous ribonucleoprotein A2/B1 on lipopolysaccharide-induced permeability of vascular endothelial cells
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摘要:

目的 探讨不均一性核糖核蛋白A2/B1(heterogeneous ribonucleoprotein A2/B1, hnRNP A2/B1)在脂多糖(lipopolysaccharide, LPS)刺激的人脐静脉内皮细胞(human umbilical vein endothelial cells, HUVECs)通透性中的作用。 方法 以HUVECs为研究对象,筛选出具有hnRNP A2/B1基因沉默作用的小干扰RNA(small interfering RNA, siRNA),按不同处理方法实验分为转染阴性对照siRNA组(NC siRNA组)、转染hnRNP A2/B1 siRNA组(hnRNP A2/B1 siRNA组)、转染阴性对照siRNA组并进行LPS干预组(NC siRNA组-LPS组)、转染hnRNP A2/B1siRNA组并进行LPS干预组(hnRNP A2/B1 siRNA组-LPS组),分别给予或不给予LPS(1 mg/L)刺激,检测不同时间点(0、6、12、24 h)各组细胞跨膜电阻抗(transendothelial electrical resistance, TEER)值,检测LPS刺激12 h后细胞表面血管内皮钙黏蛋白(vascular endothelial cadherin, VE-cadherin)及细胞间黏附分子-1(intercellular adhesion molecule-1, ICAM-1)蛋白表达变化。 结果 在相同剂量LPS诱导下,hnRNP A2/B1 siRNA-LPS组HUVECs的TEER在12 h低于NC siRNA-LPS组(P<0.05);在LPS刺激12 h后,hnRNP A2/B1 siRNA-LPS组HUVECs表面VE-cadherin表达明显低于NC siRNA-LPS组,ICAM-1表达明显高于NC siRNA-LPS组(P<0.05)。 结论 hnRNP A2/B1可能通过调节VE-cadherin及ICAM-1蛋白表达影响血管内皮细胞的通透性,发挥血管内皮屏障保护功能。

关键词: 不均一性核糖核蛋白A2/B1; 脂多糖; 内皮通透性; 细胞表面血管内皮钙黏蛋白
Abstract:

Objective To investigate the effect of heterogeneous ribonucleoprotein A2/B1 (hnRNP A2/B1) on the human umbilical vein endothelial cells (HUVECs) permeability induced by lipopolysaccharide(LPS). Methods HUVECs were used in this study, small interfering RNA (siRNA) with hnRNP A2/B1 gene silencing was screened. The samples were divided into four groups: NC siRNA group, hnRNP A2/B1 siRNA group, NC siRNA-LPS group and hnRNP A2/B1 siRNA-LPS group. The transendothelial electrical resistance (TEER) of HUVECs was detected at 0, 6, 12 h and 24 h. The expression of vascular endothelial cadherin (VE-cadherin) and intercellular adhesion molecule-1 (ICAM-1) were measured at 12 h. Results After LPS treatment, the TEER values of HUVECs in hnRNP A2/B1 siRNA-LPS group was significantly decreased compared with values of NC siRNA-LPS group at 12 h (P<0.05). The expression level of VE-cadherin in hnRNP A2/B1 siRNA-LPS group was lower than the level in the NC siRNA-LPS group, and the expression level of ICAM-1 was increased in hnRNP A2/B1 siRNA-LPS group compared with the level of NC siRNA-LPS group(P<0.05). Conclusions hnRNP A2/B1 may play an important role in vascular endothelial permeability via regulating the expression of VE-cadherin and ICAM-1, thus protecting vascular endothelial barrier function.

Key words: Heterogeneous ribonucleoprotein A2/B1; Lipopolysaccharide; Endothelial permeability; Vascular endothelial cadherin