Cardiothoracic Surgery, University of Texas Health Science Center, San Antonio, TX, USA.
Medicine/Cardiology, University of Missouri School of Medicine, Columbia, MO, USA.
J Mol Cell Cardiol. 2018 Aug;121:107-123. doi: 10.1016/j.yjmcc.2018.07.003. Epub 2018 Jul 5.
Persistent inflammation promotes development and progression of heart failure (HF). TWEAK (TNF-Related WEAK Inducer Of Apoptosis), a NF-κB- and/or AP-1-responsive proinflammatory cytokine that signals via TWEAK receptor (TWEAKR), is expressed at high levels in human and preclinical models of HF. Since the adapter molecule TRAF3IP2 (TRAF3 Interacting Protein 2) is an upstream regulator of various proinflammatory pathways, including those activated by NF-κB and AP-1, we hypothesized that targeting TRAF3IP2 inhibits TWEAK-induced proinflammatory and pro-fibrotic responses in vitro and in vivo. Consistent with the hypothesis, forced expression of TRAF3IP2 upregulated TWEAK and its receptor expression in cultured adult mouse cardiac fibroblasts (CF). Further, exogenous TWEAK upregulated TRAF3IP2 expression in a time- and dose-dependent manner, suggesting a positive-feedback regulation of TRAF3IP2 and TWEAK. TWEAK also promoted TRAF3IP2 nuclear translocation. Confirming its critical role in TWEAK signaling, silencing TRAF3IP2 inhibited TWEAK autoregulation, TWEAKR upregulation, p38 MAPK, NF-κB and AP-1 activation, inflammatory cytokine expression, MMP and TIMP1 activation, collagen expression and secretion, and importantly, proliferation and migration. Recapitulating these in vitro results, continuous infusion of TWEAK for 7 days increased systolic blood pressure (SBP), upregulated TRAF3IP2 expression, activated p38 MAPK, NF-κB and AP-1, induced the expression of multiple proinflammatory and pro-fibrotic mediators, and interstitial fibrosis in hearts of wild type mice. These proinflammatory and pro-fibrotic changes occurred in conjunction with myocardial hypertrophy and contractile dysfunction. Importantly, genetic ablation of TRAF3IP2 inhibited these TWEAK-induced adverse cardiac changes independent of increases in SBP, indicating that TRAF3IP2 plays a causal role, and thus a therapeutic target, in chronic inflammatory and fibro-proliferative diseases.
持续的炎症会促进心力衰竭(HF)的发展和进展。TWEAK(TNF 相关的弱凋亡诱导剂)是一种 NF-κB 和/或 AP-1 反应性促炎细胞因子,它在人类和 HF 的临床前模型中高表达。由于衔接分子 TRAF3IP2(TRAF3 相互作用蛋白 2)是包括 NF-κB 和 AP-1 激活的各种促炎途径的上游调节剂,我们假设靶向 TRAF3IP2 可以抑制 TWEAK 诱导的体外和体内促炎和促纤维化反应。与假设一致,TRAF3IP2 的强制表达上调了培养的成年小鼠心肌成纤维细胞(CF)中的 TWEAK 和其受体表达。此外,外源性 TWEAK 以时间和剂量依赖的方式上调 TRAF3IP2 表达,表明 TRAF3IP2 和 TWEAK 存在正反馈调节。TWEAK 还促进了 TRAF3IP2 的核转位。证实了其在 TWEAK 信号中的关键作用,沉默 TRAF3IP2 抑制了 TWEAK 的自身调节、TWEAKR 的上调、p38 MAPK、NF-κB 和 AP-1 的激活、炎症细胞因子的表达、MMP 和 TIMP1 的激活、胶原的表达和分泌,重要的是,增殖和迁移。在体外复制这些结果,连续输注 TWEAK 7 天会增加收缩压(SBP),上调 TRAF3IP2 的表达,激活 p38 MAPK、NF-κB 和 AP-1,诱导多种促炎和促纤维化介质的表达,以及野生型小鼠心脏的间质纤维化。这些促炎和促纤维化的变化伴随着心肌肥大和收缩功能障碍。重要的是,TRAF3IP2 的基因缺失抑制了这些 TWEAK 诱导的心脏不良变化,而不增加 SBP,表明 TRAF3IP2 发挥因果作用,因此是慢性炎症和纤维增生性疾病的治疗靶点。