Tang Sihui, Yue Yang, Sun Gengyun
Department of Respiratory Medicine, the First Affiliated Hospital of Anhui Medical University, Hefei 230022, Anhui, China, Corresponding author: Sun Gengyun, Email:
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2014 Nov;26(11):785-8. doi: 10.3760/cma.j.issn.2095-4352.2014.11.004.
To investigate the role of Ezrin and its phosphorylation (p-Ezrin) in the modulation of rat pulmonary microvascular endothelial cell (PMVEC) injury induced by tumor necrosis factor-α (TNF-α) and the impact of Rac 1.
Cultured PMVECs of Sprague-Dawley (SD) rats were randomly divided into time-dependent injury group induced by TNF-α and intervention group in which cells were pretreated with Rac 1 inhibitor (NSC 23766). (1) In the time-dependent injury group, Western Blot was used to detect the expression of Ezrin and p-Ezrin after 10 μg/L TNF-α stimulation for 0, 0.25, 0.5, 1, 3, 6, 12, 24 hours. (2) In the intervention group, after pre-treatment with 200 μmol/L NSC 23766 for 0.5 h, PMVECs were treated with 10 μg/L TNF-α, and the expression of p-Ezrin was detected by Western Blot after 3 hours. Besides these groups, there were control (1% fetal bovine serum simulation), single NSC 23766 or TNF-α simulation groups.
(1) Few Ezrin expression was found in PMVEC, and TNF-α could not affect Ezrin expression. p-Ezrin protein expression (p-Ezrin/Ezrin, gray scale) of PMVECs at 0 hour after TNF-α stimulation was 0.21 ± 0.03, and elevated at 0.25 hour (0.53 ± 0.19), peaked at 3 hours (1.68 ± 0.30), then it was gradually lowered, but it remained at higher level at 24 hours(0.87 ± 0.18) with significant difference (F = 62.200, P=0.000). It demonstrated that TNF-α could increase Ezrin phosphorylation in a time-dependent manner. (2) Compared with blank control group, in single NSC 23766 or TNF-α simulation group, p-Ezrin expression was induced (TNF-α group: 0.92 ± 0.12 vs. 0.68 ± 0.16, t = -2.864, P=0.020; NSC 23766 group:1.33 ± 0.24 vs. 0.68 ± 0.16, t = -5.429,P=0.000. When NSC 23766 was pre-treated with PMVECs, the expression of p-Ezrin was significantly increased compared with that in single TNF-α simulation group (2.14 ± 0.18 vs. 0.92 ± 0.12, t = -14.670, P=0.000) with significant difference (F = 73.810, P=0.000).
Ezrin proteins are phosphorylated by TNF-α. Rac 1 signaling pathway inhibition plays an important role in TNF-α-induced injury by up-regulation of p-Ezrin in PMVECs.
探讨埃兹蛋白(Ezrin)及其磷酸化形式(p-Ezrin)在肿瘤坏死因子-α(TNF-α)诱导的大鼠肺微血管内皮细胞(PMVEC)损伤调节中的作用以及Rac 1的影响。
将培养的Sprague-Dawley(SD)大鼠PMVEC随机分为TNF-α诱导的时间依赖性损伤组和用Rac 1抑制剂(NSC 23766)预处理细胞的干预组。(1)在时间依赖性损伤组中,用蛋白质免疫印迹法(Western Blot)检测10μg/L TNF-α刺激0、0.25、0.5、1、3、6、12、24小时后Ezrin和p-Ezrin的表达。(2)在干预组中,用200μmol/L NSC 23766预处理0.5小时后,PMVEC用10μg/L TNF-α处理,3小时后用Western Blot检测p-Ezrin的表达。除这些组外,还有对照组(1%胎牛血清模拟)、单独的NSC 23766或TNF-α模拟组。
(1)PMVEC中埃兹蛋白(Ezrin)表达较少,TNF-α不影响Ezrin表达。TNF-α刺激后0小时PMVEC的p-Ezrin蛋白表达(p-Ezrin/Ezrin,灰度值)为0.21±0.03,0.25小时升高(0.53±0.19),3小时达到峰值(1.68±0.30),然后逐渐降低,但24小时仍维持在较高水平(0.87±0.18),差异有统计学意义(F=62.200,P=0.000)。表明TNF-α能以时间依赖性方式增加Ezrin磷酸化。(2)与空白对照组相比,单独的NSC 23766或TNF-α模拟组中,p-Ezrin表达增加(TNF-α组:0.92±0.12对0.68±0.16,t=-2.864,P=0.020;NSC 23766组:1.33±0.24对0.68±0.16,t=-5.429,P=0.0