Hypoxia-inducible factor 1 (HIF-1) is expressed in nucleated mammalian cells in response to reduced O2 availability. HIF-1 is a basic helix-loop helix PAS transcription factor consisting of HIF-1alpha and HIF-1beta subunits HIF-1alpha expression is quantitatively regulated by cellular O2 concentration and determines the biological activity of HIF-1. The molecular mechanisms by which hypoxia is sensed and the signal is transduced leading to increased HIF-1alpha expression are not well understood. HIF-1 activates transcription of genes encoding proteins that can be classified into several groups: (i) those that increase O2 delivery to ells, such as erythropoietin and vascular endothelial growth factor (VEGF), which stimulate erythropoiesis and angiogenesis, respectively, and nitric oxide (NO) synthase-2 and heme oxygenase-1, which synthesize the vasoactive molecules NO and CO, respectively; (ii) those involved in metabolic adaptation to hypoxia such as glucose transporters and glycolytic enzymes; and (iii) other growth/survival factors, such as insulin-like growth factor 2. HIF-1 has been shown to play a critical role in the development of the circulatory system during embryogenesis and its subsequent physiological regulation in postnatal and adult life. The proposed studies are based upon the hypothesis that HIF-1 plays an important role in responses to hypoxia/ischemia by myocardial cells. For example, the role of HIF-1 in activating expression of VEGF and promoting angiogenesis in the myocardium is well established. In this project, we will focus on three questions: First, what are the mechanisms by which HIF-1 activity is induced in myocardial cells? Second, what is the effect of HIF-1 expression of myocardial viability under induced in myocardial cells? Second, what is the effect of HIF-1 expression on myocardial viability under ischemic conditions in the presence or absence of prior precondition? Third, what genes are induced by hypoxia that may contribute to the second window of preconditioning and which of these genes are regulated by HIF-1?

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
1P01HL065608-01
Application #
6369004
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
2000-09-15
Project End
2005-07-31
Budget Start
Budget End
Support Year
1
Fiscal Year
2000
Total Cost
$297,097
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Velayutham, Murugesan; Hemann, Craig F; Cardounel, Arturo J et al. (2016) Sulfite Oxidase Activity of Cytochrome c: Role of Hydrogen Peroxide. Biochem Biophys Rep 5:96-104
Long 3rd, Victor P; Bonilla, Ingrid M; Vargas-Pinto, Pedro et al. (2015) Heart failure duration progressively modulates the arrhythmia substrate through structural and electrical remodeling. Life Sci 123:61-71
Reyes, Levy A; Boslett, James; Varadharaj, Saradhadevi et al. (2015) Depletion of NADP(H) due to CD38 activation triggers endothelial dysfunction in the postischemic heart. Proc Natl Acad Sci U S A 112:11648-53
Joddar, Binata; Firstenberg, Michael S; Reen, Rashmeet K et al. (2015) Arterial levels of oxygen stimulate intimal hyperplasia in human saphenous veins via a ROS-dependent mechanism. PLoS One 10:e0120301
Xie, Lin; Talukder, M A Hassan; Sun, Jian et al. (2015) Liposomal tetrahydrobiopterin preserves eNOS coupling in the post-ischemic heart conferring in vivo cardioprotection. J Mol Cell Cardiol 86:14-22
Zheng, Xiaoxu; Zu, Lingyun; Becker, Lewis et al. (2014) Ischemic preconditioning inhibits mitochondrial permeability transition pore opening through the PTEN/PDE4 signaling pathway. Cardiology 129:163-73
Moldovan, Nicanor I; Anghelina, Mirela; Varadharaj, Saradhadevi et al. (2014) Reoxygenation-derived toxic reactive oxygen/nitrogen species modulate the contribution of bone marrow progenitor cells to remodeling after myocardial infarction. J Am Heart Assoc 3:e000471
Huang, Jie; Huffman, Jennifer E; Yamakuchi, Munekazu et al. (2014) Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2. Arterioscler Thromb Vasc Biol 34:1093-101
Chen, Yeong-Renn; Zweier, Jay L (2014) Cardiac mitochondria and reactive oxygen species generation. Circ Res 114:524-37
Tong, Jianjing; Zweier, Joseph R; Huskey, Rachael L et al. (2014) Effect of temperature, pH and heme ligands on the reduction of Cygb(Fe(3+)) by ascorbate. Arch Biochem Biophys 554:1-5

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