• DocumentCode
    1465257
  • Title

    Role of blood shear stress in the regulation of vascular smooth muscle cell migration

  • Author

    Liu, Shu Q. ; Goldman, Jeremy

  • Author_Institution
    Dept. of Biomed. Eng., Northwestern Univ., Evanston, IL, USA
  • Volume
    48
  • Issue
    4
  • fYear
    2001
  • fDate
    4/1/2001 12:00:00 AM
  • Firstpage
    474
  • Lastpage
    483
  • Abstract
    Smooth muscle cell (SMC) migration from the media to the intima of blood vessels contributes to neointimal formation and atherogenesis. Here, the authors demonstrate how blood shear stress regulates vascular SMC migration in the encapsulating tissue of a micro-cylinder implanted in the center of the rat vena cava with the micro-cylinder perpendicular to blood flow, in this model, the micro-cylinder was exposed to a laminar flow with a known shear stress field in the leading region and a vortex flow in the trailing region. After surgery, the micro-cylinder was encapsulated by a thrombus-like tissue within one day, followed by SMC migration from the vena cava to the encapsulating tissue from day 3 to 20. SMC migration was time-dependent with a peak migration speed at day 5. At each given time (excluding day 1), blood shear stress exerts an inhibitory effect on SMC migration with significantly suppressed SMC migration in the laminar flow region than in the stagnation, separation, and vortex flow regions. SMCs were relatively parallel to the shear stress direction in high shear stress regions, whereas perpendicular to the shear stress direction in low shear stress regions. These results suggest that blood shear stress plays a role in regulating SMC migration and orientation in this model.
  • Keywords
    blood vessels; cellular transport; laminar flow; vortices; 1 d; 3 to 20 d; blood shear stress; encapsulating tissue; endothelial cell migration; implanted microcylinder; intimal hyperplasia; peak migration speed; separation region; stagnation region; thrombus-like tissue; vascular smooth muscle cell migration regulation; Biomedical engineering; Blood flow; Blood vessels; Cells (biology); In vivo; Lead; Muscles; Sliding mode control; Stress; Surgery; Animals; Antigens, CD; Blood Flow Velocity; Cell Movement; Endothelium, Vascular; Granulocytes; Immunohistochemistry; Male; Models, Biological; Monocytes; Muscle, Smooth, Vascular; Prostheses and Implants; Rats; Rats, Sprague-Dawley; Stress, Mechanical; Vena Cava, Inferior;
  • fLanguage
    English
  • Journal_Title
    Biomedical Engineering, IEEE Transactions on
  • Publisher
    ieee
  • ISSN
    0018-9294
  • Type

    jour

  • DOI
    10.1109/10.915714
  • Filename
    915714