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Am J Physiol Heart Circ Physiol 284: H1778-H1784, 2003. First published January 23, 2003; doi:10.1152/ajpheart.00494.2002
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Vol. 284, Issue 5, H1778-H1784, May 2003

Uniaxial strain upregulates matrix-degrading enzymes produced by human vascular smooth muscle cells

Kazuhiko Asanuma1, Richard Magid2,3, Chad Johnson2,3, Robert M. Nerem3, and Zorina S. Galis1,2,3

1 Division of Cardiology, Department of Medicine, and 2 Department of Biomedical Engineering, Emory University School of Medicine, Atlanta 30322; and 3 The Institute of Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, Georgia 30332

Arteries remodel in response to environmental changes. We investigated whether mechanical strain modulates production of matrix metalloproteinase (MMP)-2 and -9 by cultured vascular smooth muscle cells (SMC). MMP-2 and MMP-9 expression were tested using human saphenous vein SMC cultured on silicone membranes at rest or subjected to physiological levels (5%) of stationary or cyclical (1 Hz) uniaxial strain. Compared with control, stationary strain significantly increased MMP-2 mRNA levels at all time points, whereas cyclic strain decreased it after 48 h. Both secreted and cell-associated pro-MMP-2 levels were increased by stationary strain at all times (P < 0.01), whereas cyclic strain decreased secreted levels after 48 h (P < 0.02). MMP-9 mRNA levels and pro-MMP-9 protein were increased after 48 h of stationary stretch (P < 0.01) compared with both no strain and cyclic strain. Our study indicates that vascular SMC show a selective response to different types of strain. We suggest that local increases in stationary mechanical strain resulting from stenting, hypertension, or atherosclerosis may lead to enhanced matrix degradation by SMC.

matrix metalloproteinase; mechanical stretch; vascular remodeling


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