Article date: July 2011
By: I Morecroft, B Doyle, M Nilsen, W Kolch, K Mair, MR MacLean in Volume 163, Issue 5, pages 948-963
BACKGROUND AND PURPOSE Increased pulmonary vascular remodelling, pulmonary arterial pressure and pulmonary vascular resistance characterize the development of pulmonary arterial hypertension (PAH). Activation of the Raf/mitogen‐activated protein kinase/extracellular signal‐regulated kinase (ERK)1/2 is thought to play an important role in PAH and Raf‐1 kinase inhibitor protein (RKIP), negatively regulates this pathway. This study investigated whether genetic deletion of RKIP (and hence ERK1/2 up‐regulation) resulted in a pulmonary hypertensive phenotype in mice and investigated a role for RKIP in mitogen‐regulated proliferative responses in lung fibroblasts.
EXPERIMENTAL APPROACH Pulmonary vascular haemodynamics and remodelling were assessed in mice genetically deficient in RKIP (RKIP−/−) after 2 weeks of either normoxia or hypoxia. Immunoblotting and immunohistochemistry were used to examine phosphorylation of Raf‐1, RKIP and ERK1/2 in mouse pulmonary arteries. In vitro, RKIP inhibition of mitogen signalling was analysed in CCL39 hamster lung fibroblasts.
KEY RESULTS RKIP−/− mice demonstrated elevated indices of PAH and ERK1/2 phosphorylation compared with wild‐type (WT) mice. Hypoxic RKIP−/− mice exhibited exaggerated PAH indices. Hypoxia increased phosphorylation of Raf‐1, RKIP and ERK1/2 in WT mouse pulmonary arteries and Raf‐1 phosphorylation in RKIP−/− mouse pulmonary arteries. In CCL39 cells, inhibition of RKIP potentiated mitogen‐induced proliferation and phosphorylation of RKIP, and Raf‐1.
CONCLUSIONS AND IMPLICATIONS The lack of RKIP protein resulted in a pulmonary hypertensive phenotype, exaggerated in hypoxia. Hypoxia induced phosphorylation of RKIP signalling elements in WT pulmonary arteries. RKIP inhibition potentiated mitogen‐induced proliferation in lung fibroblasts. These results provide evidence for the involvement of RKIP in suppressing the development of hypoxia‐induced PAH in mice.
DOI: 10.1111/j.1476-5381.2011.01305.x
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