Brigham and Women's Hospital/Harvard Medical School, Department of Endocrinology, Diabetes, and Hypertension, 221 Longwood Avenue, Boston, Massachusetts 02115, USA.
Endocrinology. 2010 Mar;151(3):1236-46. doi: 10.1210/en.2009-0514. Epub 2010 Jan 22.
Caveolae are the major cellular membrane structure through which extracellular mediators transmit information to intracellular signaling pathways. In vascular tissue (but not ventricular myocardium), caveolin-1 (cav-1) is the main component of caveolae; cav-1 modulates enzymes and receptors, such as the endothelial nitric oxide synthase and the angiotensin II (AngII) type 1 receptor. Evidence suggests that AngII and aldosterone (ALDO) are important mediators of ventricular injury. We have described a model of biventricular damage in rodents that relies on treatment with N-omega-nitro-l-arginine methyl ester (L-NAME (nitric oxide synthase inhibitor)) and AngII. This damage initiated at the vascular level and was observed only in the presence of ALDO and an activated mineralocorticoid receptor (MR). We hypothesize that cav-1 modulates the adverse cardiac effects mediated by ALDO in this animal model. To test this hypothesis, we assessed the ventricular damage and measures of inflammation, in wild-type (WT) and cav-1 knockout (KO) mice randomized to either placebo or L-NAME/AngII treatment. Despite displaying cardiac hypertrophy at baseline and higher blood pressure responses to L-NAME/AngII, cav-1 KO mice displayed, as compared with WT, decreased treatment-induced biventricular damage as well as decreased transcript levels of the proinflammatory marker plasminogen activator inhibitor-1. Additionally, L-NAME/AngII induced an increase in cardiac MR levels in WT but not cav-1-ablated mice. Moreover and despite similar circulating ALDO levels in both genotypes, the myocardial damage (as determined histologically and by plasminogen activator inhibitor-1 mRNA levels) was less sensitive to ALDO levels in cav-1 KO vs. WT mice, consistent with decreased MR signaling in the cav-1 KO. Thus, we conclude that the L-NAME/AngII-induced biventricular damage is mediated by a mechanism partially dependent on cav-1 and signaling via MR/ALDO.
小窝是细胞外介质将信息传递到细胞内信号通路的主要细胞膜结构。在血管组织(但不是心室心肌)中,窖蛋白-1(cav-1)是小窝的主要成分;cav-1 调节酶和受体,如内皮型一氧化氮合酶和血管紧张素 II(AngII)型 1 受体。有证据表明,AngII 和醛固酮(ALDO)是心室损伤的重要介质。我们已经描述了一种依赖于 N-ω-硝基-L-精氨酸甲酯(L-NAME(一氧化氮合酶抑制剂))和 AngII 治疗的啮齿动物双心室损伤模型。这种损伤始于血管水平,仅在存在 ALDO 和激活的盐皮质激素受体(MR)的情况下观察到。我们假设 cav-1 调节这种动物模型中 ALDO 介导的不良心脏效应。为了验证这一假设,我们评估了野生型(WT)和窖蛋白-1 敲除(KO)小鼠的心室损伤和炎症标志物,这些小鼠被随机分配到安慰剂或 L-NAME/AngII 治疗组。尽管在基线时显示出心脏肥大和对 L-NAME/AngII 的更高血压反应,但与 WT 相比,cav-1 KO 小鼠显示出减少的治疗诱导的双心室损伤以及促炎标志物纤溶酶原激活物抑制剂-1 的转录水平降低。此外,L-NAME/AngII 在 WT 但不是 cav-1 缺失的小鼠中诱导心脏 MR 水平增加。此外,尽管两种基因型的循环 ALDO 水平相似,但心肌损伤(通过组织学和纤溶酶原激活物抑制剂-1 mRNA 水平确定)在 cav-1 KO 小鼠中对 ALDO 水平的敏感性低于 WT 小鼠,与 cav-1 KO 中的 MR 信号降低一致。因此,我们得出结论,L-NAME/AngII 诱导的双心室损伤是由部分依赖于 cav-1 的机制介导的,该机制通过 MR/ALDO 信号传递。