Walczak Cécile, Gaignier Fanny, Gilet Alexandre, Zou Feng, Thornton Simon N, Ropars Armelle
University of Henri Poincaré, Vandoeuvre-les-Nacy, France.
Biochim Biophys Acta. 2011 Dec;1813(12):2125-32. doi: 10.1016/j.bbamcr.2011.07.010. Epub 2011 Jul 23.
Aldosterone is now recognised as an important actor in inflammation processes. Neoangiogenesis plays a crucial role in this complex process and immune cells, such as neutrophils, appear to be able to secrete different forms of (pro)angiogenic molecules, especially VEGF-A. The present work was undertaken to investigate whether aldosterone was able to regulate VEGF-A production in human neutrophils. The HL-60 (progranulocytic) cell line and human polymorphonuclear leukocytes were incubated for different time periods with aldosterone. Total cellular RNA extraction, submitted to reverse transcription and real time semi-quantitative PCR, was used to study VEGF-A mRNA expression. Cell supernatants were collected and ELISA tests were performed to analyse VEGF-A protein production. Aldosterone increased VEGF-A mRNA and protein expression in a dose- and time-dependent manner in both cell types. Inhibitors of PI3 kinases, ERK1/2, and to a lesser extent of p38 MAPK, decreased this aldosterone-induced immune cell activation. Western-blot performed with HL-60 cells confirmed that ERK1/2 and p38 MAPK pathways were stimulated by aldosterone. Mineralocorticoid receptors are implicated in this VEGF-A up-regulation because HL-60 cells pre-treated with spironolactone, an aldosterone receptor antagonist, diminished the effects of aldosterone. Aldosterone was also able to increase VEGF-A production of phagocytic cells such as neutrophils. These results suggest that this hormone could play an active role in the neovascularisation process by favouring entry of plasma proteins and fluids into the vascular wall, cell proliferation and tissue rebuilding.
醛固酮现已被认为是炎症过程中的一个重要因素。新生血管生成在这一复杂过程中起着关键作用,免疫细胞,如中性粒细胞,似乎能够分泌不同形式的(促)血管生成分子,尤其是血管内皮生长因子A(VEGF-A)。本研究旨在探讨醛固酮是否能够调节人中性粒细胞中VEGF-A的产生。将HL-60(早幼粒细胞)细胞系和人多形核白细胞与醛固酮孵育不同时间段。提取细胞总RNA,进行逆转录和实时半定量PCR,以研究VEGF-A mRNA的表达。收集细胞上清液并进行酶联免疫吸附测定(ELISA)试验,以分析VEGF-A蛋白的产生。醛固酮在两种细胞类型中均以剂量和时间依赖性方式增加VEGF-A mRNA和蛋白的表达。磷脂酰肌醇-3激酶(PI3激酶)、细胞外信号调节激酶1/2(ERK1/2)的抑制剂,以及在较小程度上p38丝裂原活化蛋白激酶(p38 MAPK)的抑制剂,均可降低醛固酮诱导的免疫细胞活化。用HL-60细胞进行的蛋白质免疫印迹法(Western-blot)证实,ERK1/2和p38 MAPK信号通路受到醛固酮的刺激。盐皮质激素受体参与了这种VEGF-A的上调,因为用醛固酮受体拮抗剂螺内酯预处理的HL-60细胞可减弱醛固酮的作用。醛固酮还能够增加吞噬细胞如中性粒细胞的VEGF-A产生。这些结果表明,这种激素可能通过促进血浆蛋白和液体进入血管壁、细胞增殖和组织重建,在新血管形成过程中发挥积极作用。