Title :
cDNA microarray analysis of human umbilical vein endothelial cells subjected to cyclic mechanical strain
Author :
Frye, Stacie R. ; Eskin, Suzanne G. ; McIntire, Larry V.
Author_Institution :
Dept. of Bioeng., Rice Univ., Houston, TX, USA
Abstract :
Endothelial cells are constantly subjected to mechanical forces due to blood flow. The forces have been implicated in vascular pathogenesis; therefore, the consequences of these forces need to be examined. Using cDNA microarray technology, we studied the gene expression of human umbilical vein endothelial cells subjected to a 10% cyclic strain for 6 and 24 hours. Of the 4000 genes included on the Research Genetics GeneFilter® 211, thirty genes were determined as differentially expressed. The most highly upregulated gene at 6 hours was carboxypeptidase A3 at 3.2-fold; whereas, the most downregulated gene was dystrobrevin, alpha at 0.4-fold. At 24 hours, the most highly upregulated was matrix metalloproteinase 10 at 3.6-fold and the most downregulated was secretory leukocyte protease inhibitor at 0.5-fold. These genes were not only regulated by the strain of the cells, but some were actually regulated by the fluid agitation inherent in the system over the cells.
Keywords :
DNA; biochemistry; biological techniques; biomechanics; cellular biophysics; genetics; haemorheology; proteins; 24 hour; 6 hour; Research Genetics GeneFilter; blood flow; cDNA microarray analysis; carboxypeptidase A3; cells; cyclic mechanical strain; cyclic strain; downregulated gene; dystrobrevin; fluid agitation; gene expression; human umbilical vein endothelial cells; matrix metalloproteinase; mechanical forces; secretory leukocyte protease inhibitor; upregulated gene; vascular pathogenesis; Blood flow; Capacitive sensors; Cells (biology); Gene expression; Genetics; Humans; Inhibitors; Pathogens; Veins; White blood cells;
Conference_Titel :
Engineering in Medicine and Biology, 2002. 24th Annual Conference and the Annual Fall Meeting of the Biomedical Engineering Society EMBS/BMES Conference, 2002. Proceedings of the Second Joint
Print_ISBN :
0-7803-7612-9
DOI :
10.1109/IEMBS.2002.1137002