Department of Cardiovascular Diseases, Renmin Hospital of Wuhan University, Wuhan City, China.
Mol Cells. 2011 Sep;32(3):235-41. doi: 10.1007/s10059-011-1026-z. Epub 2011 Aug 23.
Tumor necrosis factor-α (TNF-α) plays an important role in pathological angiogenesis associated with inflammatory response. Pim-3 kinase belonging to serine/threonine protein kinases is a potent suppressor of myc-induced apoptosis. We have recently demonstrated that Pim-3 plays an essential role in endothelial cell (EC) spreading and migration. In this study, we showed that TNF-α transiently increased Pim-3 mRNA expression, and this was mediated through Tumor necrosis factor-α receptor-1 (TNFR1) pathway in ECs. TNF-α could promote stabilization of Pim- 3 mRNA in ECs. Small-interfering RNA (siRNA)-mediated gene knockdown of Pim-3 significantly impaired TNF-α-induced formation of EC membrane protrusions in vitro. Furthermore, Pim-3 silencing inhibited EC sprouting in subcutaneous Matrigel in vivo. eNOS mRNA abundance was lower in Pim-3 siRNA transfected ECs compared with the control ECs. These observations suggest that Pim-3 plays a role in TNF-α-induced angiogenesis.
肿瘤坏死因子-α(TNF-α)在与炎症反应相关的病理性血管生成中发挥重要作用。属于丝氨酸/苏氨酸蛋白激酶的 Pim-3 激酶是 Myc 诱导的细胞凋亡的有效抑制剂。我们最近证明 Pim-3 在血管内皮细胞(EC)的扩展和迁移中起着至关重要的作用。在这项研究中,我们表明 TNF-α 可短暂增加 Pim-3 mRNA 的表达,这是通过 EC 中的肿瘤坏死因子-α受体-1(TNFR1)途径介导的。TNF-α 可促进 Pim-3 mRNA 在 EC 中的稳定。小干扰 RNA(siRNA)介导的 Pim-3 基因敲低显著损害了 TNF-α诱导的 EC 膜突起的体外形成。此外,Pim-3 沉默抑制了体内皮下 Matrigel 中的 EC 发芽。与对照 EC 相比,转染了 Pim-3 siRNA 的 EC 中的 eNOS mRNA 丰度较低。这些观察结果表明 Pim-3 在 TNF-α 诱导的血管生成中发挥作用。