Liang Xiao, Luo Xiao-Lin, Zhong Hua, Hu Qing-Hua, He Fang
Department of Pathophysiology, Medical College of Shihezi University, Shihezi, China.
Sheng Li Xue Bao. 2012 Jun 25;64(3):289-95.
To investigate the effect of Ca(2+)-sensing receptor (CaR) on Spermine-induced extracellular Ca(2+) influx and NO generation in human umbilical vein endothelial cells (HUVEC), the small interference RNA (siRNA) specifically targeting CaR gene was designed, synthesized and transfected into HUVEC according to the cDNA sequence of human CaR gene in GenBank. The transfection efficiency and the interference efficiency of CaR protein were determined by laser scanning confocal microscopy and Western blot, respectively. Intracellular Ca(2+) concentration (Ca(2+)) was measured by Fura-2/AM loading. The production of NO and the activity of endothelial nitric oxide synthase (eNOS) were determined by the DAF-FM diacetate (DAF-FM DA). Western blot results demonstrated that siRNA targeting the CaR specifically decreased the expression of CaR protein in CaR siRNA group 48 h after transfection (P < 0.05). At the same time, the Spermine-induced Ca(2+), eNOS activity and NO generation were also significantly reduced (P < 0.05) in CaR siRNA group compared with those in the untransfected or negative siRNA transfected group. In conclusion, the present study suggests that the CaR plays an important role in the Spermine-evoked process of extracellular Ca(2+) influx and NO generation in HUVEC.
为研究钙敏感受体(CaR)对精胺诱导的人脐静脉内皮细胞(HUVEC)细胞外钙内流及一氧化氮(NO)生成的影响,根据GenBank中人CaR基因的cDNA序列设计、合成了特异性靶向CaR基因的小干扰RNA(siRNA),并将其转染至HUVEC。分别通过激光扫描共聚焦显微镜和蛋白质免疫印迹法检测转染效率及CaR蛋白的干扰效率。采用Fura-2/AM负载法测定细胞内钙离子浓度([Ca²⁺]i)。用二乙酸二氨基荧光素(DAF-FM DA)检测NO的生成及内皮型一氧化氮合酶(eNOS)的活性。蛋白质免疫印迹结果显示,靶向CaR的siRNA转染48 h后,CaR siRNA组中CaR蛋白的表达显著降低(P<0.05)。同时,与未转染组或阴性siRNA转染组相比,CaR siRNA组中精胺诱导的[Ca²⁺]i、eNOS活性及NO生成也显著降低(P<0.05)。综上所述,本研究表明CaR在精胺诱发的HUVEC细胞外钙内流及NO生成过程中起重要作用。