Pulmonary hypertension (PH) is a complex, progressive syndrome leading to right ventricular (RV) failure and death. RV dysfunction predicts morbidity and mortality in PH. Considerable variability exists in the RV hypertrophy and dysfunction that develops in patients with PH, suggesting susceptibility differences in the RV response to PH. little is known about the mechanisms that drive the RV response, and potential regulatory factors remain undetermined. The pluripotential cytokine MIF (macrophage migration inhibitory factor) has described roles in regulating changes in cardiomyocyte glucose metabolism observed in the pressure- overloaded RV in animal models of PH. Interestingly;the cytokine also has roles in the regulation of myocyte and vascular endothelial cell apoptosis, vascular smooth muscle cell prostacyclin synthesis, and vascular inflammation. Our preliminary studies show that chronic hypoxia induces MIF expression selectively in the RV of C57 BL/6 mice. Furthermore, MIF-deficient mice show diminished RV hypertrophy in response to chronic hypoxia. The studies proposed in the current application are designed to determine if MIF has a functional role in the regulation of the RV response to chronic hypoxia, potentially through its role in regulating myocyte glucose metabolism and energy supply. Specifically, we will define the mechanisms by which hypoxia induces MIF expression in RV of mice and in cardiomyocytes in vitro. We will subsequently use knockout mice with absent MIF expression to determine whether MIF is required for RV hypertrophy and/or dysfunction in response to hypoxia. Finally, we will measure activation of MIF-dependent signaling pathways involved in myocyte glycolysis and glucose uptake in wild type and MIF-null mice exposed to chronic hypoxia to determine whether the cytokine is required for metabolic regulation. These studies will establish a regulatory role for MIF in the RV response to PH, and may help to clarify the links between RV hypertrophy, metabolic change, ventricular dysfunction, and failure. In the long term, the proposed studies may be relevant to future studies designed to develop RV-specific therapies for PH. They may also identify MIF as a bio-marker in patients with PH to monitor progression to RV failure so that treatment strategies can be adjusted accordingly.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32HL110516-02
Application #
8474600
Study Section
Special Emphasis Panel (ZRG1-F10A-S (20))
Program Officer
Meadows, Tawanna
Project Start
2011-07-15
Project End
2013-06-30
Budget Start
2012-07-15
Budget End
2013-06-30
Support Year
2
Fiscal Year
2012
Total Cost
$59,792
Indirect Cost
Name
Johns Hopkins University
Department
None
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Kolb, Todd M; Peabody, Jacelyn; Baddoura, Philip et al. (2015) Right Ventricular Angiogenesis is an Early Adaptive Response to Chronic Hypoxia-Induced Pulmonary Hypertension. Microcirculation 22:724-36
Kolb, Todd M; Hassoun, Paul M (2012) Right ventricular dysfunction in chronic lung disease. Cardiol Clin 30:243-56