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Polarization of plasma membrane microviscosity during endothelial cell migration
Amit Vasanji1, Prabar K Ghosh, Linda M Graham
1Department of Cell Biology, Lerner Research Institute, Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
Developmental Cell
|January 16, 2004
Summary
Cholesterol increases plasma membrane microviscosity (PMM) at the cell leading edge, influencing actin dynamics. This PMM modulation enhances endothelial cell migration by promoting actin network formation.
Area of Science:
- Cell biology
- Biophysics
- Endothelial cell function
Background:
- Cell movement relies on polarized cell structures.
- Endothelial cells (ECs) exhibit anterior-posterior polarization during migration.
- Plasma membrane properties are critical for cell motility.
Purpose of the Study:
- To investigate the role of plasma membrane microviscosity (PMM) in endothelial cell migration.
- To determine the influence of cholesterol on PMM and actin dynamics.
- To elucidate the relationship between PMM, actin polymerization, and cell movement speed.
Main Methods:
- Utilized synthetic lipid vesicles to study membrane microviscosity effects on actin dynamics.
- Employed live-cell imaging to analyze PMM and actin polymerization in migrating ECs.
- Stimulated ECs with angiogenic growth factors to observe migration responses.
Main Results:
- Plasma membrane microviscosity (PMM) is elevated at the leading edge of migrating ECs.
- Cholesterol plays a key role in establishing the PMM gradient.
- Increased PMM showed a biphasic effect on actin dynamics, enhancing vesicle deformation at low concentrations and inhibiting it at high concentrations.
- Migrating ECs with increased PMM exhibited reduced actin polymerization rates but enhanced cell movement.
Conclusions:
- Elevated PMM at the cell front is a feature of migrating ECs.
- Increased PMM, influenced by cholesterol, is crucial for regulating actin dynamics.
- Higher PMM in lamellipodia may facilitate efficient actin network formation, leading to faster endothelial cell migration.