Queen's University - Utility Bar

QSpace at Queen's University >
Theses, Dissertations & Graduate Projects >
Queen's Theses & Dissertations >

Please use this identifier to cite or link to this item: http://hdl.handle.net/1974/1980

Title: The Role of Ca²⁺/CaM-Stimulated Phosphodiesterase 1C in Vascular Smooth Muscle cells of the Synthetic/Activated Phenotype
Authors: Ross, ANDREW

Files in This Item:

File Description SizeFormat
Ross_Andrew_J_200907_MSc.pdf1.85 MBAdobe PDFView/Open
Keywords: PDE1C
VSMC
Issue Date: 2009
Series/Report no.: Canadian theses
Abstract: Manipulations to cyclic nucleotide populations show considerable promise in the treatment of vasculopathies associated with luminal narrowing and PDE inhibition currently represents one of the most selective methods of clinically modifying levels of these second messengers. Many cardiovascular diseases are associated with a change in vascular smooth muscle cell (VSMC) phenotype, resulting in a hyperproliferative cell devoid of contractile properties. This cell has been defined as “synthetic/activated” and differs from the normal “contractile/quiescent” VSMC in several aspects. Previous investigations have established that phosphodiesterase 1C (PDE1C), a PDE not produced in contractile/quiescent VSMCs is upregulated, and the functionally dominant PDE in the presence of calcium in these cells. This study looked to establish a role for PDE1C in synthetic/activated VSMCs as it relates to the management of VSMC phenotype. Herein, we show that RNAi mediated knockdown of PDE1C decreased expression of phenotype-dependent markers in HASMCs including PDGF-alpha receptor, l-caldesmon, and TRPC1, while the expression of other markers, including PKG, vinculin, and beta-1 integrin were unaffected. Treatment with PDE1C siRNA also reduced cell migration, proliferation, and the ability of HASMCs to bind extracellular matrix proteins. These effects were mediated without any major changes in global cAMP levels. Furthermore, a novel interaction between PDE1C and the TRPC cation channel was identified that may establish a role for PDE1C in calcium-cAMP mediation. These findings establish an important role for PDE1C in the synthetic/activated HASMC, both phenotypically, and at the sub-cellular level.
Description: Thesis (Master, Pharmacology & Toxicology) -- Queen's University, 2009-07-02 19:02:52.281
URI: http://hdl.handle.net/1974/1980
Appears in Collections:Queen's Theses & Dissertations
Pharmacology & Toxicology Graduate Theses

Items in QSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

  DSpace Software Copyright © 2002-2008  The DSpace Foundation - TOP