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Getting the actin filaments straight: nucleation-release or treadmilling?
1Institute of Molecular Biology, Austrian Academy of Sciences, A-5020 Salzburg, Billrothstrasse 11, Austria.
Trends in Cell Biology
|February 1, 1995
Summary
Actin filament dynamics are crucial for cell movement. New data suggest long, treadmilling filaments, not short ones, drive cell motility through lateral flow in lamellipodia.
Area of Science:
- Cell Biology
- Biophysics
- Cytoskeleton Dynamics
Background:
- Actin filament dynamics are essential for cell locomotion in metazoans.
- Previous models, like 'nucleation-release,' proposed short, non-oriented filaments in lamellipodia based on caged actin probe experiments.
- Recent structural data challenge this model, suggesting long actin filaments with graded lengths.
Purpose of the Study:
- To re-evaluate models of actin-based cell motility in light of new structural data.
- To investigate the role of actin filament organization and dynamics in lamellipodia movement.
- To reconcile conflicting experimental findings regarding filament length and organization.
Main Methods:
- Analysis of structural data from keratocyte cytoskeletons.
- Integration of previous findings on cytoskeleton-substrate interactions.
- Comparative analysis of different actin dynamics models.
Main Results:
- Recent structural data are inconsistent with the 'nucleation-release' model.
- The data support a model involving treadmilling of long actin filaments of varying lengths.
- The cell cytoskeleton remains stationary relative to the substrate during movement.
Conclusions:
- The 'nucleation-release' model for keratocyte motility is likely incorrect.
- Long actin filaments undergoing treadmilling are more consistent with observed structures.
- Lateral filament flow is a potential mechanism driving lamellipodia motility, reconciling structural data and cell movement.