NO-independent cGMP regulation of vascular remodeling
Project Number1R01HL081720-01A2
Contact PI/Project LeaderTULIS, DAVID A
Awardee OrganizationNORTH CAROLINA CENTRAL UNIVERSITY
Description
Abstract Text
Vascular smooth muscle (VSM) cyclic guanosine 3',5'-moriophosphate (cGMP) serves as a critical
regulator of many cellular functions that contribute to vessel growth after injury. Nitric oxide (NO) and
carbon monoxide (CO) operate as soluble guanylate cyclase (sGC)-activating ligands for cGMP synthesis;
however, limitations of NO and CO signaling warrant study into alternate, pathophysiologically relevant
routes for cGMP control. Provocative new findings challenge the traditional notion that cGMP exerts
vascular protection through cGMP-dependent protein kinase type (cGKI) and suggest that cGMP may
operate via cAMP/cAK to promote vascular protection. Current studies in our laboratory focus on novel NOindependent
approaches for cGMP control as significant basic science tools and as potential cardiovascular
therapeutics. Preliminary data support a role for vascular growth control by NO-independent cGMP and
suggest mechanistic involvement of matrix metalloproteinase (MMP)-2 and MMP-9. The long-term objective
of this research project is to investigate strategies for cGMP control of VSM growth, and the central
hypothesis of this proposal is that NO-independent cGMP protects against vascular growth and that this
occurs through cAK signals. Two Specific Aims will be used to test this hypothesis:
Aim 1 will analyze the roles of NO-independent cGMP and cGMP-directed cGKI/cAK signaling in
attenuating vascular remodeling in the rat balloon injury and mouse wire denudation injury models.
Aim 2 will examine matrix-based mechanisms including cell migration and MMP balance that underlie
cGMP-mediated growth control in rat and mouse primary VSM cells.
Pharmacology, RNA interference, and viral gene delivery approaches will be used, and conditional VSMspecific
cGKI-deficient models will allow direct comparison of cGKI versus cAK mechanisms. Results are
anticipated to provide insight into and further evidence for NO-independent cGMP control of the injury
growth response in VSM and shed light upon cGMP-directed MMPs in mediating these events.
Injuries and diseases of the heart and blood vessels are wide-ranging and very serious public health
concerns, and statistics show they are still the major cause of death in American populations. We believe
that results from these studies will shed light on some novel and promising strategies that could be used to
minimize the severity of blood vessel injury and disease and may offer beneficial prospects for further study
in basic science research and human-based clinical studies.
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