Endothelium-derived relaxing factor, identified as nitric oxide (NO), is a key mediator regulating vascular tone and blood pressure. NO mediates vascular relaxation through activation of soluble guanylate cyclase (sGC) in the smooth muscle. While NO is synthesized by a specific well characterized NO synthase in the endothelium (eNOS), the process of vascular NO degradation and metabolism is poorly understood. It is hypothesized that NO degradation in the vessel wall is mediated by an O2-dependent NO dioxygenase (NOD) that oxidizes NO to nitrate. However, the identity of the specific NO dioxygenase that serves as the main in vivo regulator of O2- dependent NO degradation in vascular smooth muscle has remained elusive. Cytoglobin (Cgb) is a recently discovered globin expressed in smooth muscle with unknown function. Based on our preliminary data where we observe that: 1) Cgb is the major globin expressed in smooth muscle; and 2) knockout of Cgb greatly prolongs NO decay, increases vascular relaxation, lowers blood pressure and systemic vascular resistance, we hypothesize that Cgb is the major heme protein regulating the rate of O2-dependent NO metabolism in the vessel wall, in turn profoundly modulating vascular tone. In this grant, there are 3 aims in which we sequentially test this hypothesis, first in vascular smooth muscle cells, then in isolated vessels and finally in the in vivo cardiovascular system with experimental measurements and computational modeling. The latter will enable us to determine how well the process of Cgb-mediated O2-dependent NO metabolism accounts for the measured vascular NO metabolism along with enabling prediction of the effects of modulating Cgb expression and NOD function. Since the O2-dependent NOD function of Cgb is controlled by its rate of reduction, studies will be performed to elucidate the process and mechanisms of Cgb reduction in smooth muscle cells, vessels and in vivo in mice utilizing molecular knockdown, pharmacological inhibition, or other manipulation of these reducing pathways. We will determine how modulation of the NOD function of Cgb modulates vascular tone in normal physiology and vascular disease with studies in vessels and mice with varying Cgb expression levels and inhibition of each of the major pathways of its reduction or specific inhibition of its NOD function. These studies will be performed in normal mice and mice with angiotensin-induced hypertension. In these settings, studies will be performed to measure and scavenge superoxide (O2-.) to determine how the O2-dependent reaction of NO with Cgb compares to that of O2-. and specific attention paid to the role of the endothelium and the coupling state of eNOS in NO metabolism. Accomplishment of this research plan will elucidate the molecular mechanism underlying the important role of Cgb in vascular NO metabolism and provide important insights into the regulation of vascular tone in normal physiology and cardiovascular disease. This work will illuminate the path leading to development of novel therapeutic approaches to reverse vascular dysfunction and ameliorate secondary disease through modulation of the process of NO degradation.

Public Health Relevance

Nitric oxide (NO) regulates vascular tone and blood pressure; however, the process of vascular NO degradation and metabolism is not well understood. Cytoglobin (Cgb) is a recently discovered globin expressed in smooth muscle. We hypothesize that Cgb is the major heme protein regulating the rate of O2- dependent NO metabolism in the vessel wall, in turn, profoundly modulating vascular tone. We will test this hypothesis in smooth muscle cells, isolated vessels and in vivo to determine how Cgb functions to modulate vascular tone in normal physiology and disease. This work will elucidate the mechanism of vascular NO metabolism and the regulation of vascular tone in normal physiology and cardiovascular disease, leading to development of novel therapeutics to reverse vascular dysfunction and disease.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL131941-02
Application #
9405608
Study Section
Vascular Cell and Molecular Biology Study Section (VCMB)
Program Officer
Charette, Marc F
Project Start
2017-01-01
Project End
2020-12-31
Budget Start
2018-01-01
Budget End
2018-12-31
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Ohio State University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210
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Zhou, Danlei; Hemann, Craig; Boslett, James et al. (2017) Oxygen binding and nitric oxide dioxygenase activity of cytoglobin are altered to different extents by cysteine modification. FEBS Open Bio 7:845-853
Liu, Xiaoping; El-Mahdy, Mohamed A; Boslett, James et al. (2017) Cytoglobin regulates blood pressure and vascular tone through nitric oxide metabolism in the vascular wall. Nat Commun 8:14807