The endothelial cell (EC) cytoskeleton mediates several biological functions such as adhesion, migration, phagocytosis, cell division, and mechanosensitivity. These functions are carried out in part through dynamic cytoskeletal polymerization, modulation of crosslinking, and development of tension between intracellular organelles and the extracellular matrix via focal adhesion plaques. One important component of the cytoskeleton is actin which polymerizes into filaments and is thought to be prestressed by virtue of crosslinking proteins such as α-actinin, filamin and myosin II molecular motors. Additionally, actomyosin interaction has been hypothesized to act as a stress dissipation mechanism by virtue of dynamic crossbridging which facilitates actin diffusion through the polymer network of the cytoplasm (Humphrey et al., 2002).
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ASME 2008 Summer Bioengineering Conference
June 25–29, 2008
Marco Island, Florida, USA
Conference Sponsors:
- Bioengineering Division
ISBN:
978-0-7918-4321-5
PROCEEDINGS PAPER
Interaction of Shear Stress, Myosin II, and Actin in Dynamic Modulation of Endothelial Cell Microrheology
Jhanvi H. Dangaria,
Jhanvi H. Dangaria
The Pennsylvania State University, University Park, PA
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Peter J. Butler
Peter J. Butler
The Pennsylvania State University, University Park, PA
Search for other works by this author on:
Jhanvi H. Dangaria
The Pennsylvania State University, University Park, PA
Peter J. Butler
The Pennsylvania State University, University Park, PA
Paper No:
SBC2008-192947, pp. 63-64; 2 pages
Published Online:
March 13, 2014
Citation
Dangaria, JH, & Butler, PJ. "Interaction of Shear Stress, Myosin II, and Actin in Dynamic Modulation of Endothelial Cell Microrheology." Proceedings of the ASME 2008 Summer Bioengineering Conference. ASME 2008 Summer Bioengineering Conference, Parts A and B. Marco Island, Florida, USA. June 25–29, 2008. pp. 63-64. ASME. https://doi.org/10.1115/SBC2008-192947
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