Kapitsinou Pinelopi P, Rajendran Ganeshkumar, Astleford Lindsay, Michael Mark, Schonfeld Michael P, Fields Timothy, Shay Sheila, French Jaketa L, West James, Haase Volker H
Departments of Medicine, Anatomy, and Cell Biology, University of Kansas Medical Center, Kansas City, Kansas, USA The Kidney Institute, University of Kansas Medical Center, Kansas City, Kansas, USA Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee, USA
Departments of Medicine, Anatomy, and Cell Biology, University of Kansas Medical Center, Kansas City, Kansas, USA The Kidney Institute, University of Kansas Medical Center, Kansas City, Kansas, USA.
Mol Cell Biol. 2016 May 2;36(10):1584-94. doi: 10.1128/MCB.01055-15. Print 2016 May 15.
Hypoxia-inducible factors 1 and 2 (HIF-1 and -2) control oxygen supply to tissues by regulating erythropoiesis, angiogenesis and vascular homeostasis. HIFs are regulated in response to oxygen availability by prolyl-4-hydroxylase domain (PHD) proteins, with PHD2 being the main oxygen sensor that controls HIF activity under normoxia. In this study, we used a genetic approach to investigate the endothelial PHD2/HIF axis in the regulation of vascular function. We found that inactivation of Phd2 in endothelial cells specifically resulted in severe pulmonary hypertension (∼118% increase in right ventricular systolic pressure) but not polycythemia and was associated with abnormal muscularization of peripheral pulmonary arteries and right ventricular hypertrophy. Concurrent inactivation of either Hif1a or Hif2a in endothelial cell-specific Phd2 mutants demonstrated that the development of pulmonary hypertension was dependent on HIF-2α but not HIF-1α. Furthermore, endothelial HIF-2α was required for the development of increased pulmonary artery pressures in a model of pulmonary hypertension induced by chronic hypoxia. We propose that these HIF-2-dependent effects are partially due to increased expression of vasoconstrictor molecule endothelin 1 and a concomitant decrease in vasodilatory apelin receptor signaling. Taken together, our data identify endothelial HIF-2 as a key transcription factor in the pathogenesis of pulmonary hypertension.
缺氧诱导因子1和2(HIF-1和-2)通过调节红细胞生成、血管生成和血管稳态来控制组织的氧气供应。HIFs由脯氨酰-4-羟化酶结构域(PHD)蛋白根据氧气可用性进行调节,其中PHD2是在常氧条件下控制HIF活性的主要氧气传感器。在本研究中,我们采用遗传学方法研究内皮细胞PHD2/HIF轴在血管功能调节中的作用。我们发现,内皮细胞中Phd2的失活特异性地导致严重的肺动脉高压(右心室收缩压增加约118%),但不会导致红细胞增多症,并且与外周肺动脉的异常肌化和右心室肥大有关。在内皮细胞特异性Phd2突变体中同时失活Hif1a或Hif2a表明,肺动脉高压的发展依赖于HIF-2α而非HIF-1α。此外,在慢性缺氧诱导的肺动脉高压模型中,内皮HIF-2α是肺动脉压力升高所必需的。我们认为,这些依赖于HIF-2的效应部分归因于血管收缩分子内皮素1表达的增加以及血管舒张肽apelin受体信号传导的相应减少。综上所述,我们的数据确定内皮HIF-2是肺动脉高压发病机制中的关键转录因子。