Cyclic strain inhibits acute pro-inflammatory gene expression in aortic valve interstitial cells

Biomechanics and Modeling in Mechanobiology

Volumn 9, Issue 1, 2010, Pages 117-125

  Smith, Kathryn E ^a   Metzler, Scott A ^a   Warnock, James N ^a  

^a MISSISSIPPI STATE UNIVERSITY   (United States)

Author keywords

Cyclic strain; Heart valve; Inflammation; Interstitial cells; Tissue engineering

Indexed keywords

AORTIC VALVES; CYCLIC STRAIN; EXPRESSION LEVELS; HEART VALVE; HEART VALVES; IN-VITRO; IN-VIVO; INFLAMMATION; INFLAMMATORY GENES; PHYSIOLOGICAL CONDITION; PHYSIOLOGICAL LEVELS; POTENTIAL MECHANISM; PRE-CONDITIONING; Q-RT-PCR; STRAIN MAGNITUDE; TISSUE DEVELOPMENT; TISSUE-ENGINEERED HEART; VALVE INTERSTITIAL CELLS;

BIOACTIVITY; CONFOCAL MICROSCOPY; GENE EXPRESSION; HEART; IMAGE STORAGE TUBES; PATHOLOGY; PHOSPHORYLATION; TISSUE; TISSUE ENGINEERING;

VALVES (MECHANICAL);

AUTACOID; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; MESSENGER RNA; MONOCYTE CHEMOTACTIC PROTEIN 1; OSTEOPONTIN; VASCULAR CELL ADHESION MOLECULE 1;

ANIMAL; AORTA VALVE; ARTICLE; CONFOCAL MICROSCOPY; GENE EXPRESSION REGULATION; GENETICS; MECHANICAL STRESS; METABOLISM; PATHOLOGY; SWINE;

ANIMALS; AORTIC VALVE; CHEMOKINE CCL2; GENE EXPRESSION REGULATION; GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR; INFLAMMATION MEDIATORS; MICROSCOPY, CONFOCAL; OSTEOPONTIN; RNA, MESSENGER; STRESS, MECHANICAL; SUS SCROFA; VASCULAR CELL ADHESION MOLECULE-1;

EID: 74349083160     PISSN: 16177959     EISSN: 16822978     Source Type: Journal    
DOI: 10.1007/s10237-009-0165-2     Document Type: Article

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