Dept. of Pharmacology, College of Medicine, Univ. of Illinois, 835 South Wolcott Ave., Chicago, IL 60612, USA.
Am J Physiol Cell Physiol. 2010 Mar;298(3):C656-64. doi: 10.1152/ajpcell.00456.2009. Epub 2009 Dec 23.
NF-kappaB signaling is known to induce the expression of antiapoptotic and proinflammatory genes in endothelial cells (ECs). We have shown recently that Ca(2+) influx through canonical transient receptor potential (TRPC) channels activates NF-kappaB in ECs. Here we show that Ca(2+) influx signal prevents thrombin-induced apoptosis by inducing NF-kappaB-dependent A20 expression in ECs. Knockdown of TRPC1 expressed in human umbilical vein ECs with small interfering RNA (siRNA) suppressed thrombin-induced Ca(2+) influx and NF-kappaB activation in ECs. Interestingly, we observed that thrombin induced >25% of cell death (apoptosis) in TRPC1-knockdown ECs whereas thrombin had no effect on control or control siRNA-transfected ECs. To understand the basis of EC survival, we performed gene microarray analysis using ECs. Thrombin stimulation increased only a set of NF-kappaB-regulated genes 3- to 14-fold over basal levels in ECs. Expression of the antiapoptotic gene A20 was the highest among these upregulated genes. Like TRPC1 knockdown, thrombin induced apoptosis in A20-knockdown ECs. To address the importance of Ca(2+) influx signal, we measured thrombin-induced A20 expression in control and TRPC1-knockdown ECs. Thrombin-induced p65/RelA binding to A20 promoter-specific NF-kappaB sequence and A20 protein expression were suppressed in TRPC1-knockdown ECs compared with control ECs. Furthermore, in TRPC1-knockdown ECs, thrombin induced the expression of proapoptotic proteins caspase-3 and BAX. Importantly, thrombin-induced apoptosis in TRPC1-knockdown ECs was prevented by adenovirus-mediated expression of A20. These results suggest that Ca(2+) influx via TRPC channels plays a critical role in the mechanism of cell survival signaling through A20 expression in ECs.
NF-κB 信号通路已知可诱导内皮细胞(ECs)中抗凋亡和促炎基因的表达。我们最近表明,通过经典瞬时受体电位(TRPC)通道的 Ca2+内流可激活 ECs 中的 NF-κB。在这里,我们表明 Ca2+内流信号通过在 ECs 中诱导 NF-κB 依赖性 A20 表达来防止凝血酶诱导的细胞凋亡。用小干扰 RNA(siRNA)敲低人脐静脉 ECs 中表达的 TRPC1 可抑制 ECs 中凝血酶诱导的 Ca2+内流和 NF-κB 激活。有趣的是,我们观察到凝血酶诱导的 TRPC1 敲低 ECs 中超过 25%的细胞死亡(凋亡),而凝血酶对对照或对照 siRNA 转染的 ECs 没有影响。为了了解 EC 存活的基础,我们使用 ECs 进行了基因微阵列分析。凝血酶刺激仅使一组 NF-κB 调节基因的表达在 ECs 中比基础水平增加 3-14 倍。在这些上调基因中,抗凋亡基因 A20 的表达最高。与 TRPC1 敲低一样,凝血酶诱导 A20 敲低 ECs 中的细胞凋亡。为了研究 Ca2+内流信号的重要性,我们在对照和 TRPC1 敲低 ECs 中测量了凝血酶诱导的 A20 表达。与对照 ECs 相比,TRPC1 敲低 ECs 中凝血酶诱导的 p65/RelA 与 A20 启动子特异性 NF-κB 序列结合和 A20 蛋白表达受到抑制。此外,在 TRPC1 敲低 ECs 中,凝血酶诱导了促凋亡蛋白 caspase-3 和 BAX 的表达。重要的是,通过腺病毒介导的 A20 表达可防止 TRPC1 敲低 ECs 中的凝血酶诱导的细胞凋亡。这些结果表明,通过 TRPC 通道的 Ca2+内流在通过 ECs 中 A20 表达的细胞存活信号机制中发挥关键作用。