The Research Institute at Nationwide Children's Hospital, 700 Children's Drive, Columbus, OH 43205, USA.
Am J Physiol Heart Circ Physiol. 2010 May;298(5):H1518-28. doi: 10.1152/ajpheart.00813.2009. Epub 2010 Feb 19.
The mitogen-activated protein (MAP) kinases are involved in cellular responses to many stimuli, including hypoxia. MAP kinase signaling is regulated by a family of phosphatases that include MAP kinase phosphatase-1 (MKP-1). We hypothesized that mice lacking the Mkp-1 gene would have exaggerated chronic hypoxia-induced pulmonary hypertension. Wild-type (WT) and Mkp-1(-/-) mice were exposed to either 4 wk of normoxia or hypobaric hypoxia. Following chronic hypoxia, both genotypes demonstrated elevated right ventricular pressures, right ventricular hypertrophy as demonstrated by the ratio of the right ventricle to the left ventricle plus septum weights [RV(LV + S)], and greater vascular remodeling. However, the right ventricular systolic pressures, the RV/(LV + S), and the medial wall thickness of 100- to 300-microm vessels was significantly greater in the Mkp-1(-/-) mice than in the WT mice following 4 wk of hypobaric hypoxia. Chronic hypoxic exposure caused no detectable change in eNOS protein levels in the lungs in either genotype; however, Mkp-1(-/-) mice had lower levels of eNOS protein and lower lung NO production than did WT mice. No iNOS protein was detected in the lungs by Western blotting in any condition in either genotype. Both arginase I and arginase II protein levels were greater in the lungs of hypoxic Mkp-1(-/-) mice than those in hypoxic WT mice. Lung levels of proliferating cell nuclear antigen were greater in hypoxic Mkp-1(-/-) than in hypoxic WT mice. These data are consistent with the concept that MKP-1 acts to restrain hypoxia-induced arginase expression and thereby reduces vascular remodeling and the severity of pulmonary hypertension.
丝裂原活化蛋白(MAP)激酶参与细胞对许多刺激的反应,包括缺氧。MAP 激酶信号转导受一系列磷酸酶调节,包括 MAP 激酶磷酸酶-1(MKP-1)。我们假设缺乏 Mkp-1 基因的小鼠会出现更严重的慢性缺氧性肺动脉高压。野生型(WT)和 Mkp-1(-/-)小鼠分别暴露于常氧或低压缺氧 4 周。慢性缺氧后,两种基因型的右心室压力均升高,右心室肥厚(以右心室与左心室加室间隔重量比[RV(LV + S)]表示),血管重构增加。然而,在 4 周低压缺氧后,Mkp-1(-/-)小鼠的右心室收缩压、RV/(LV + S)和 100-300μm 血管的中膜厚度明显大于 WT 小鼠。慢性缺氧暴露在两种基因型中均未引起肺中 eNOS 蛋白水平的可检测变化;然而,Mkp-1(-/-)小鼠的 eNOS 蛋白水平和肺 NO 产生量均低于 WT 小鼠。在任何基因型的任何条件下,Western blot 均未检测到肺中的 iNOS 蛋白。在缺氧的 Mkp-1(-/-)小鼠的肺中,精氨酸酶 I 和精氨酸酶 II 的蛋白水平均高于缺氧的 WT 小鼠。缺氧的 Mkp-1(-/-)小鼠的肺中增殖细胞核抗原的水平高于缺氧的 WT 小鼠。这些数据与 MKP-1 可抑制缺氧诱导的精氨酸酶表达从而减少血管重构和肺动脉高压严重程度的概念一致。