Department of Biomedical Sciences, College of Veterinary Medicine, University of Missouri, Columbia, MO, USA.
Department of Biomedical Sciences, College of Veterinary Medicine, University of Missouri, Columbia, MO, USA.
J Mol Cell Cardiol. 2019 Nov;136:1-14. doi: 10.1016/j.yjmcc.2019.08.011. Epub 2019 Aug 29.
Cardiomyocyte survival and death contributes to many cardiac diseases. A common mechanism of cardiomyocyte death is through apoptosis however, numerous death receptors (DR) have been virtually unstudied in the context of cardiovascular disease. Previous studies have identified TNF-related apoptosis inducing ligand (TRAIL) and its receptor, DR5, as being altered in a chronic catecholamine administration model of heart failure, and suggest a role of non-canonical signaling in cardiomyocytes. Furthermore, multiple clinical studies have identified TRAIL or DR5 as biomarkers in the prediction of severity and mortality following myocardial infarction and in heart failure development risk suggesting a role of DR5 signaling in the heart. While TRAIL/DR5 have been extensively studied as a potential cancer therapeutic due to their ability to selectively activate apoptosis in cancer cells, TRAIL and DR5 are highly expressed in the heart where their function is uncharacterized. However, many non-transformed cell types are resistant to TRAIL-induced apoptosis suggesting non-canonical functions in non-cancerous cell types. Our goal was to determine the role of DR5 in the heart with the hypothesis that DR5 does not induce cardiomyocyte apoptosis but initiates non-canonical signaling to promote cardiomyocyte growth and survival. Histological analysis of hearts from mice treated with a DR5 agonists showed increased hypertrophy with no differences in cardiomyocyte death, fibrosis or function. Mechanistic studies in the heart and isolated cardiomyocytes identified ERK1/2 activation with DR5 agonist treatment which contributed to hypertrophy. Furthermore, epidermal growth factor receptor (EGFR) was activated following DR5 agonist treatment through activation of MMP and HB-EGFR cleavage and specific inhibitors of MMP and EGFR prevented DR5-mediated ERK1/2 signaling and hypertrophy. Taken together, these studies identify a previously unidentified role for DR5 in the heart, which does not promote apoptosis but acts through non-canonical MMP-EGFR-ERK1/2 signaling mechanisms to contribute to cardiomyocyte hypertrophy.
心肌细胞的存活和死亡导致了许多心脏疾病。细胞凋亡是心肌细胞死亡的一种常见机制,但在心血管疾病背景下,许多死亡受体(DR)几乎没有被研究过。先前的研究已经确定 TNF 相关凋亡诱导配体(TRAIL)及其受体 DR5 在慢性儿茶酚胺给药心力衰竭模型中发生改变,并提示非经典信号在心肌细胞中发挥作用。此外,多项临床研究已经确定 TRAIL 或 DR5 是心肌梗死后严重程度和死亡率以及心力衰竭发展风险的预测生物标志物,提示 DR5 信号在心脏中的作用。虽然 TRAIL/DR5 因其能够选择性地激活癌细胞中的凋亡而被广泛研究作为一种潜在的癌症治疗方法,但 TRAIL 和 DR5 在心脏中高度表达,其功能尚未确定。然而,许多非转化细胞类型对 TRAIL 诱导的凋亡具有抗性,这表明在非癌细胞类型中具有非经典功能。我们的目标是确定 DR5 在心脏中的作用,假设 DR5 不会诱导心肌细胞凋亡,而是启动非经典信号以促进心肌细胞生长和存活。用 DR5 激动剂处理的小鼠心脏的组织学分析显示,心肌肥大增加,而心肌细胞死亡、纤维化或功能没有差异。心脏和分离的心肌细胞中的机制研究表明,DR5 激动剂治疗会激活 ERK1/2,这有助于心肌肥大。此外,DR5 激动剂处理后通过 MMP 和 HB-EGFR 切割激活表皮生长因子受体(EGFR),并且 MMP 和 EGFR 的特异性抑制剂可阻止 DR5 介导的 ERK1/2 信号和肥大。总之,这些研究确定了 DR5 在心脏中的一个以前未被识别的作用,它不会促进凋亡,而是通过非经典的 MMP-EGFR-ERK1/2 信号机制发挥作用,有助于心肌细胞肥大。