The purpose of the Cardiac and Myocyte Physiology Core D is to provide required methods for the evaluation of the effects of glycoconjugate modifications on myocyte, muscle fiber, and intact heart physiology. Two in vitro methods and two non-invasive in vivo methods are employed. For Projects 1, 2 and 3, we will use isolated adult myocytes to determine the impact of protein modification on sarcomere shortening and relaxation, and on the whole cell calcium transient. Resting and adrenergic stimulated cells are studied. Myocyte isolation from adult heart models also are provided to the project for molecular studies and for the isolation of mitochondria. For Projects 2 and 3 we will provide isolated heart Langendorff preparations, to define organ function, and to provide tissue for additional analysis using models of ischemia/reperfusion and preconditioning. For Projects 1 and 5, the Core will determine cardiac function using non-invasive echo-Doppler imaging analysis over a fime-line for the animal models used. Mouse models of atherosclerosis on varying diets are a major focus of this analysis. Lastly, for Projects 2 and 3, we will determine vascular properties such as large artery stiffness using Doppler imaging of aortic flow at two locations and determination of pulse wave velocity. We have a wide variety of state-of-the-art methods to evaluate cardiac functions and some of the specific studies will be determined by the inifial data obtained.

Public Health Relevance

Core D provides important physiologic assessment of the glycoconjugate modifications to be studied in the Program. Glycoproteins and glycolipids are thought to impact vascular and cardiac physiology, contributing to features of both heart and vessel disease. Determination of the physiology of both systems, as appropriate for the model studied will be an important component of the Program's overall research strategy.

National Institute of Health (NIH)
National Heart, Lung, and Blood Institute (NHLBI)
Research Program Projects (P01)
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Special Emphasis Panel (ZHL1-CSR-H)
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Johns Hopkins University
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Yang, Shuang; Rubin, Abigail; Eshghi, Shadi Toghi et al. (2016) Chemoenzymatic method for glycomics: Isolation, identification, and quantitation. Proteomics 16:241-56
Lam, Maggie P Y; Venkatraman, Vidya; Xing, Yi et al. (2016) Data-Driven Approach To Determine Popular Proteins for Targeted Proteomics Translation of Six Organ Systems. J Proteome Res 15:4126-4134
Fahie, Kamau; Zachara, Natasha E (2016) Molecular Functions of Glycoconjugates in Autophagy. J Mol Biol 428:3305-24
Yang, Weiming; Jackson, Brooks; Zhang, Hui (2016) Identification of glycoproteins associated with HIV latently infected cells using quantitative glycoproteomics. Proteomics 16:1872-80
Hardivillé, Stéphan; Hart, Gerald W (2016) Nutrient regulation of gene expression by O-GlcNAcylation of chromatin. Curr Opin Chem Biol 33:88-94
Miller, William P; Mihailescu, Maria L; Yang, Chen et al. (2016) The Translational Repressor 4E-BP1 Contributes to Diabetes-Induced Visual Dysfunction. Invest Ophthalmol Vis Sci 57:1327-37
Zhu, Yanping; Liu, Ta-Wei; Madden, Zarina et al. (2016) Post-translational O-GlcNAcylation is essential for nuclear pore integrity and maintenance of the pore selectivity filter. J Mol Cell Biol 8:2-16
Hou, Ching-Wen; Mohanan, Vishnu; Zachara, Natasha E et al. (2016) Identification and biological consequences of the O-GlcNAc modification of the human innate immune receptor, Nod2. Glycobiology 26:13-8
Ma, Junfeng; Hart, Gerald W (2016) Mass Spectrometry-Based Quantitative O-GlcNAcomic Analysis. Methods Mol Biol 1410:91-103
Lagerlöf, Olof; Slocomb, Julia E; Hong, Ingie et al. (2016) The nutrient sensor OGT in PVN neurons regulates feeding. Science 351:1293-6

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