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Pressure-Induced Vascular Oxidative Stress Is Mediated Through Activation of Integrin-Linked Kinase 1/βPIX/Rac-1 Pathway

Title: Pressure-Induced Vascular Oxidative Stress Is Mediated Through Activation of Integrin-Linked Kinase 1/βPIX/Rac-1 Pathway
Authors: Vecchione, Carmine; Carnevale, Daniela; Di Pardo, Alba; Gentile, Maria Teresa; Damato, Antonio; Cocozza, Germana; Antenucci, Giovanna; Mascio, Giada; Bettarini, Umberto; Landolfi, Alessandro; Iorio, Luca; Maffei, Angelo; Lembo, Giuseppe
Source: Hypertension ; volume 54, issue 5, page 1028-1034 ; ISSN 0194-911X 1524-4563
Publisher Information: Ovid Technologies (Wolters Kluwer Health)
Publication Year: 2009
Description: High blood pressure induces a mechanical stress on vascular walls and evokes oxidative stress and vascular dysfunction. The aim of this study was to characterize the intracellular signaling causing vascular oxidative stress in response to pressure. In carotid arteries subjected to high pressure levels, we observed not only an impaired vasorelaxation, increased superoxide production, and NADPH oxidase activity, but also a concomitant activation of Rac-1, a small G protein. Selective inhibition of Rac-1, with an adenovirus carrying a dominant-negative Rac-1 mutant, significantly reduced NADPH oxidase activity and oxidative stress and, more importantly, rescued vascular function in carotid arteries at high pressure. The analysis of molecular events associated with mechanotransduction demonstrated at high pressure levels an overexpression of integrin-linked kinase 1 and its recruitment to plasma membrane interacting with paxillin. The inhibition of integrin-linked kinase 1 by small interfering RNA impaired Rac-1 activation and rescued oxidative stress–induced vascular dysfunction in response to high pressure. Finally, we showed that βPIX, a guanine-nucleotide exchange factor, is the intermediate molecule recruited by integrin-linked kinase 1, converging the intracellular signaling toward Rac-1–mediated oxidative vascular dysfunction during pressure overload. Our data demonstrate that biomechanical stress evoked by high blood pressure triggers an integrin-linked kinase 1/βPIX/Rac-1 signaling, thus generating oxidative vascular dysfunction.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1161/hypertensionaha.109.136572
DOI: 10.1161/HYPERTENSIONAHA.109.136572
Availability: https://doi.org/10.1161/hypertensionaha.109.136572; https://www.ahajournals.org/doi/full/10.1161/HYPERTENSIONAHA.109.136572
Accession Number: edsbas.D2C6F5C
Database: BASE