Mitra Sumegha, Wade Michael S, Sun Xiaoguang, Moldobaeva Nurgul, Flores Carlos, Ma Shwu-Fan, Zhang Wei, Garcia Joe G N, Jacobson Jeffrey R
Division of Pulmonary, Critical Care, Sleep and Allergy, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States of America.
Centro de Investigacion Biomedica en red Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain; Research Unit, Hospital Universitario Nuestra Senora de Candelaria, Tenerife, Spain.
PLoS One. 2014 Jun 18;9(6):e100169. doi: 10.1371/journal.pone.0100169. eCollection 2014.
Growth arrest DNA damage inducible alpha (GADD45a) is a stress-induced gene we have shown to participate in the pathophysiology of ventilator-induced lung injury (VILI) via regulation of mechanical stress-induced Akt ubiquitination and phosphorylation. The regulation of GADD45a expression by mechanical stress and its relationship with acute lung injury (ALI) susceptibility and severity, however, remains unknown.
We examined mechanical stress-dependent regulatory elements (MSRE) in the GADD45a promoter and the contribution of promoter polymorphisms in GADD45a expression and ALI susceptibility.
Initial studies in GADD45a knockout and heterozygous mice confirmed the relationship of GADD45a gene dose to VILI severity. Human lung endothelial cells (EC) transfected with a luciferase vector containing the full length GADD45a promoter sequence (-771 to +223) demonstrated a >4 fold increase in GADD45a expression in response to 18% cyclic stretch (CS, 4 h) compared to static controls while specific promoter regions harboring CS-dependent MSRE were identified using vectors containing serial deletion constructs of the GADD45a promoter. In silico analyses of GADD45a promoter region (-371 to -133) revealed a potential binding site for specificity protein 1 (SP1), a finding supported by confirmed SP1 binding with the GADD45a promoter and by the significant attenuation of CS-dependent GADD45a promoter activity in response to SP1 silencing. Separately, case-control association studies revealed a significant association of a GADD45a promoter SNP at -589 (rs581000, G>C) with reduced ALI susceptibility. Subsequently, we found allelic variation of this SNP is associated with both differential GADD45a expression in mechanically stressed EC (18% CS, 4 h) and differential binding site of interferon regulatory factor 7 (IRF7) at this site.
These results strongly support a functional role for GADD45a in ALI/VILI and identify a specific gene variant that confers risk for ALI.
生长停滞DNA损伤诱导蛋白α(GADD45a)是一种应激诱导基因,我们已经证明它通过调节机械应激诱导的Akt泛素化和磷酸化参与呼吸机诱导的肺损伤(VILI)的病理生理学过程。然而,机械应激对GADD45a表达的调节及其与急性肺损伤(ALI)易感性和严重程度的关系仍不清楚。
我们研究了GADD45a启动子中机械应激依赖性调节元件(MSRE)以及启动子多态性对GADD45a表达和ALI易感性的影响。
对GADD45a基因敲除和杂合小鼠的初步研究证实了GADD45a基因剂量与VILI严重程度之间的关系。用含有全长GADD45a启动子序列(-771至+223)的荧光素酶载体转染人肺内皮细胞(EC),与静态对照相比,在18%的循环拉伸(CS,4小时)刺激下,GADD45a的表达增加了4倍以上,同时使用含有GADD45a启动子系列缺失构建体的载体鉴定了含有CS依赖性MSRE的特定启动子区域。对GADD45a启动子区域(-371至-133)的计算机分析揭示了特异性蛋白1(SP1)的潜在结合位点,SP1与GADD45a启动子的结合以及SP1沉默后CS依赖性GADD45a启动子活性的显著减弱证实了这一发现。另外,病例对照关联研究显示,GADD45a启动子-589处的单核苷酸多态性(rs581000,G>C)与ALI易感性降低显著相关。随后,我们发现该单核苷酸多态性的等位基因变异与机械应激EC(18%CS,4小时)中GADD45a的差异表达以及干扰素调节因子7(IRF7)在此位点的差异结合位点有关。
这些结果有力地支持了GADD45a在ALI/VILI中的功能作用,并确定了一种赋予ALI风险的特定基因变异。