The goal of this project is to re-invent concepts regarding the regulation, targeting, and particularly the translational use of protein kinase G (PKG) activation for the goal of treating myocardial disease. PKG is the primary enzyme activated by the second messenger cyclic GMP (cGMP) and a prominent regulator of vascular tone. Its role in the cardiomyocyte has been more controversial, but growing evidence shows that stimulating PKG provides a potent anti-stress and pathophysiological brake, countering pro- hypertrophic/fibrotic signaling, mechano-sensing and arrhythmia, and improving diastolic function. New data from our lab now shows it can also profoundly impact microRNA formation, protein quality control, and autophagy. Cyclic GMP is generated by either a nitric oxide or natriuretic peptide signaling-pathway. While both have long been viewed as interchangeable, our recent work shows prominent differences in their role and regulation in the cardiomyocyte. They operate in nano-domains regulated by specific phospho- diesterases; notably PDE5 and PDE9 that target NO and NP stimulated cGMP, respectively. Thus, how one activates PK effectively depends upon the disease condition and thus how cGMP is being generated, which PDEs are involved, and even the post-translational state of PKG. For example, oxidative stress, which depresses NO-stimulated cGMP also oxidizes PKG, which we showed reduces its protective effects while also altering its response to agonists. Estrogen depletion impairs NO-stimulated cGMP in females, compromising PKG activation strategies dependent on this pathway. This R35 program develops four innovative research programs aimed at ultimately improving our therapeutic use of PKG activation: 1) Dissect nano-domain controls, defining protein partners, selective PKG kinase targets, their dynamics in varying diseases, and how they can be more effectively regulated; 2) Identify how co-morbidities such as obesity, metabolic syndrome, and post- menopause limit PKG activation strategies, and develop methods to circumvent them; 3) Discover novel signaling by which PKG activation provides benefit, including new roles in autophagy, proteosome trafficking, pathological mechanosensing and transcriptional controls; and 4) Develop a PKG proteotype using new proteomic methods applied to human heart biopsies and blood. Through this work, we aim to transform concepts of PKG therapy for heart disease, based on its biology to derive an effective personalized approach.

Public Health Relevance

This program focuses on the control and effective therapeutic use of activating the enzyme PKG1 to treat cardiac muscle disease. The work is multi-scale ? ranging all the way from analysis of nanodomains where the enzyme is regulated to its protein interactions, new effects on the heart in health and disease, through to studies of human hearts to determine how it is impacted by heart failure. Using new tools we will decipher how PKG1 is controlled in the heart, and develop a personalized medical approach to its use in patients.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Unknown (R35)
Project #
5R35HL135827-02
Application #
9404050
Study Section
Special Emphasis Panel (ZHL1)
Program Officer
Adhikari, Bishow B
Project Start
2017-01-01
Project End
2023-12-31
Budget Start
2018-01-01
Budget End
2018-12-31
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21205
Hsu, Steven; Kokkonen-Simon, Kristen M; Kirk, Jonathan A et al. (2018) Right Ventricular Myofilament Functional Differences in Humans With Systemic Sclerosis-Associated Versus Idiopathic Pulmonary Arterial Hypertension. Circulation 137:2360-2370
Kokkonen-Simon, Kristen M; Saberi, Amir; Nakamura, Taishi et al. (2018) Marked disparity of microRNA modulation by cGMP-selective PDE5 versus PDE9 inhibitors in heart disease. JCI Insight 3:
Wang, Sheng-Bing; Venkatraman, Vidya; Crowgey, Erin L et al. (2018) Protein S-Nitrosylation Controls Glycogen Synthase Kinase 3? Function Independent of Its Phosphorylation State. Circ Res 122:1517-1531
Nakamura, Taishi; Zhu, Guangshuo; Ranek, Mark J et al. (2018) Prevention of PKG-1? Oxidation Suppresses Antihypertrophic/Antifibrotic Effects From PDE5 Inhibition but not sGC Stimulation. Circ Heart Fail 11:e004740
Hashimoto, Toru; Kim, Grace E; Tunin, Richard S et al. (2018) Acute Enhancement of Cardiac Function by Phosphodiesterase Type 1 Inhibition. Circulation 138:1974-1987
Tampakakis, Emmanouil; Shah, Sanjiv J; Borlaug, Barry A et al. (2018) Pulmonary Effective Arterial Elastance as a Measure of Right Ventricular Afterload and Its Prognostic Value in Pulmonary Hypertension Due to Left Heart Disease. Circ Heart Fail 11:e004436
Rouf, Rosanne; MacFarlane, Elena Gallo; Takimoto, Eiki et al. (2017) Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice. JCI Insight 2:
Sharma, Kavita; Kass, David A (2017) Inorganic Nitrates:Qifor Heart Failure With Preserved Ejection Fraction? Circ Res 120:1057-1059
Chung, Heaseung Sophia; Kim, Grace E; Holewinski, Ronald J et al. (2017) Transient receptor potential channel 6 regulates abnormal cardiac S-nitrosylation in Duchenne muscular dystrophy. Proc Natl Acad Sci U S A 114:E10763-E10771
Cho, Gun-Sik; Lee, Dong I; Tampakakis, Emmanouil et al. (2017) Neonatal Transplantation Confers Maturation of PSC-Derived Cardiomyocytes Conducive to Modeling Cardiomyopathy. Cell Rep 18:571-582

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