Activation of protein kinase C and disruption of endothelial monolayer integrity by sodium arsenite-Potential mechanism in the development of atherosclerosis

Toxicology and Applied Pharmacology

Volumn 220, Issue 2, 2007, Pages 164-177

  Pereira, Flavia E ^a   Coffin, J Douglas ^a   Beall, Howard D ^a  

^a UNIVERSITY OF MONTANA   (United States)

Author keywords

Catenin; PKC ; Sodium arsenite; Stress fibers; Vascular permeability; VE cadherin

Indexed keywords

ACTIN; ARSENIC; ARSENITE SODIUM; BETA CATENIN; PROTEIN KINASE C; PROTEIN KINASE C ALPHA; VASCULAR ENDOTHELIAL CADHERIN;

ARTICLE; ATHEROSCLEROSIS; CELL JUNCTION; CELL MEMBRANE PERMEABILITY; CONCENTRATION RESPONSE; CONTROLLED STUDY; CYTOSKELETON; DISEASE EXACERBATION; ENDOTHELIUM CELL; ENZYME ACTIVATION; EXPOSURE; HUMAN; HUMAN CELL; IMMUNOFLUORESCENCE; MONOLAYER CULTURE; PROTEIN PHOSPHORYLATION; STAINING; STRESS FIBER; TIME;

ARSENITES; ATHEROSCLEROSIS; BETA CATENIN; BLOTTING, WESTERN; CADHERINS; CAPILLARY PERMEABILITY; CARBAZOLES; CELLS, CULTURED; DOSE-RESPONSE RELATIONSHIP, DRUG; ENDOTHELIAL CELLS; ENZYME ACTIVATION; ENZYME INHIBITORS; FLUORESCENT ANTIBODY TECHNIQUE; GAP JUNCTIONS; HUMANS; IMMUNOPRECIPITATION; INDOLES; PROTEIN KINASE C; SODIUM COMPOUNDS;

EID: 34047120058     PISSN: 0041008X     EISSN: 10960333     Source Type: Journal    
DOI: 10.1016/j.taap.2006.12.035     Document Type: Article

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