Rahman A, Swärd K
Division of Vascular and Airway Research, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Acta Physiol (Oxf). 2009 Feb;195(2):231-45. doi: 10.1111/j.1748-1716.2008.01907.x. Epub 2008 Sep 25.
Caveolae are omega-shaped membrane invaginations present in essentially all cell types in the cardiovascular system, and numerous functions have been ascribed to these structures. Caveolae formation depends on caveolins, cholesterol and polymerase I and transcript release factor-Cavin (PTRF-Cavin). The current review summarizes and critically discusses the cardiovascular phenotypes reported in caveolin-1-deficient mice. Major changes in the structure and function of heart, lung and blood vessels have been documented, suggesting that caveolae play a critical role at the interface between blood and surrounding tissue. According to an emerging paradigm, many of these changes are secondary to uncoupling of endothelial nitric oxide synthase. Thus, nitric oxide synthase not only synthesizes more nitric oxide in the absence of caveolin-1, but also more superoxide with potential pathogenic consequences. It is further argued that the vasodilating drive from increased nitric oxide production in caveolin-1-deficient mice is balanced by changes in the vascular media that favour increased dynamic resistance regulation. Harnessing the therapeutic opportunities buried in caveolae, while challenging, could expand the arsenal of treatment options in cancer, lung disease and atherosclerosis.
小窝是呈Ω形的膜内陷结构,存在于心血管系统的几乎所有细胞类型中,并且这些结构具有多种功能。小窝的形成依赖于小窝蛋白、胆固醇以及聚合酶I和转录释放因子-窖蛋白(PTRF-窖蛋白)。本综述总结并批判性地讨论了在小窝蛋白-1基因敲除小鼠中报道的心血管表型。心脏、肺和血管的结构和功能发生了重大变化,这表明小窝在血液与周围组织的界面处起着关键作用。根据一种新出现的模式,这些变化中的许多是内皮型一氧化氮合酶解偶联的继发结果。因此,一氧化氮合酶不仅在缺乏小窝蛋白-1的情况下合成更多的一氧化氮,还会产生更多具有潜在致病后果的超氧化物。进一步的观点认为,小窝蛋白-1基因敲除小鼠中一氧化氮生成增加所产生的血管舒张驱动力,被血管中膜有利于增加动态阻力调节的变化所平衡。利用小窝中蕴藏的治疗机会虽然具有挑战性,但可能会扩大癌症、肺部疾病和动脉粥样硬化的治疗选择范围。