Therapeutic potential of the epidermal growth factor receptor transactivation in hypertension: a convergent signaling pathway of vascular tone, oxidative stress, and hypertrophic growth downstream of vasoactive G-protein-coupled receptors?This paper is one of a selection of papers published in this Special Issue, entitled Young Investigators' Forum.
- 1 January 2007
- journal article
- review article
- Published by Canadian Science Publishing in Canadian Journal of Physiology and Pharmacology
- Vol. 85 (1) , 97-104
- https://doi.org/10.1139/y06-097
Abstract
The concurrence of enhanced vascular tone, oxidative stress, and hypertrophic growth is a hallmark of hypertension, the condition characterized by sustained elevated blood pressure. However, it is unclear how and why such apparently distinct processes coincide in hypertension. Elevated levels of certain vasoactive G-protein-coupled receptor agonists (such as catecholamines, endothelin-1, and angiotensin II) can explain, at least in part, the development and progression of many hypertensive disorders. Here, we review findings made by other investigators and ourselves suggesting that enhanced vascular tone, oxidative stress, and hypertrophic growth characteristically induced by these agonists involve the transactivation of growth factor receptors. The first step in this transactivation mechanism is agonist-induced activation of metalloproteinase-dependent shedding of growth factors. Shed growth factors then trigger intracellular signaling cascades necessary for growth, production of reactive oxygen species, and maintenance of vascular tone. If this hypothesis is proven generally correct, then transactivation blockers have general therapeutic potential in hypertension regardless of the causative agonist.Keywords
This publication has 56 references indexed in Scilit:
- Oxidative stress and vascular remodellingExperimental Physiology, 2005
- Inward Remodeling of the Rabbit Aorta Is Blocked by the Matrix Metalloproteinase Inhibitor DoxycyclineJournal of Vascular Research, 2004
- The vascular NAD(P)H oxidases as therapeutic targets in cardiovascular diseasesTrends in Pharmacological Sciences, 2003
- Doxycycline Modulates Smooth Muscle Cell Growth, Migration, and Matrix Remodeling after Arterial InjuryThe American Journal of Pathology, 2002
- Cardiac hypertrophy is inhibited by antagonism of ADAM12 processing of HB-EGF: Metalloproteinase inhibitors as a new therapyNature Medicine, 2002
- Reactive Oxygen Species and Signal TransductionIUBMB Life, 2001
- c-Jun N-terminal Kinase Activation by Hydrogen Peroxide in Endothelial Cells Involves Src-dependent Epidermal Growth Factor Receptor TransactivationJournal of Biological Chemistry, 2001
- Environmental-Dependent Acceleration of a Developmental Switch: The Floral TransitionScience's STKE, 2000
- Elastase and matrix metalloproteinase inhibitors induce regression, and tenascin-C antisense prevents progression, of vascular diseaseJournal of Clinical Investigation, 2000
- N -Acetyl-Cysteine Decreases the Matrix-Degrading Capacity of Macrophage-Derived Foam CellsCirculation, 1998