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Related Concept Videos

Cell Migration01:09

Cell Migration

Cell migration, the process by which cells move from one location to another, is essential for the proper development and viability of organisms throughout their life. When cells are not able to migrate properly to their ordained locations, various disorders may occur. For example, disruption in cell migration causes chronic inflammatory diseases such as arthritis.
Cell Migration01:19

Cell Migration

Cell migration is a process by which the cells move from one location to another, playing an essential role in embryological development, repair and regeneration, immune response, and metastasis. Cells migrate in response to chemical or mechanical signals generated by specific organs or tissues. The overall mechanism includes three steps - polarization, protrusion, and release. Polarization involves the formation of a distinct cell front and rear, which determines the direction of movement.
Types of Membrane Protrusions01:28

Types of Membrane Protrusions

The protrusion of the cell surface is an initial step for several cellular processes, including cell migration, phagocytosis, and neurite outgrowth. These membrane protrusions are a result of cytoskeletal rearrangement. The most  widely observed cell protrusions include lamellipodia, pseudopodia, filopodia, microvilli, invadopodia, and podosomes. These protrusions can be of two types — static or dynamic.
The microvilli, an example of stable protrusions, are finger-like projections with a...
Mechanism of Lamellipodia Formation01:31

Mechanism of Lamellipodia Formation

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Actin Polymerization and Cell Motility01:13

Actin Polymerization and Cell Motility

Actin is a family of globular proteins that are highly abundant in eukaryotic cells. It makes up approximately 1-5% of total cell protein concentration. Actin monomers polymerize to form a complex network of polarized filaments, the actin cytoskeleton, that plays a crucial role in many cellular processes, including cell motility, division, endocytosis, and metastasis of cancer cells.
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Role of Myosin in Cell Migration

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Related Experiment Video

Updated: Jun 2, 2026

Protrusion Force Microscopy: A Method to Quantify Forces Developed by Cell Protrusions
06:37

Protrusion Force Microscopy: A Method to Quantify Forces Developed by Cell Protrusions

Published on: June 16, 2018

Theoretical model for cellular shapes driven by protrusive and adhesive forces.

Doron Kabaso1, Roie Shlomovitz, Kathrin Schloen

  • 1Department of Chemical Physics, The Weizmann Institute of Science, Rehovot, Israel.

Plos Computational Biology
|May 17, 2011
PubMed
Summary

This study presents a theoretical model to explain how cell shapes are influenced by forces from the actin cytoskeleton and adhesion to the extracellular matrix. The model simulates the evolution of cell contours beyond the point where spontaneous protrusions form. It shows that different forces lead to distinct cell shapes, such as those seen in lamellipodia. The researchers found that as the strength of protrusive forces decreases, the cell stabilizes into a regular pattern of protrusions. This result may help explain why cell shape varies depending on the properties of the surrounding matrix. The model incorporates curvature-sensitive membrane complexes that influence the shape of the cell. The findings provide a theoretical framework for understanding how internal and external forces shape the cell. The study highlights the importance of feedback between membrane shape and force generation. The authors suggest that further research could explore how the model applies to different cell types.

Keywords:
actin cytoskeletoncell morphologyextracellular matrixlamellipodia formation

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Area of Science:

  • Cell biophysics
  • Theoretical cell biology
  • Cytoskeletal mechanics

Background:

Cell shape is influenced by forces generated by the actin cytoskeleton, including protrusive and adhesive forces. Prior research has shown that these forces contribute to the formation of cellular structures like lamellipodia. However, the specific mechanisms by which these forces lead to stable cell shapes remain unclear. No prior work had resolved how the interplay between membrane curvature and force generation affects the final morphology. This gap motivated the development of a theoretical framework to explore the relationship between membrane shape and the forces acting on it. The model aims to bridge the gap between linear instability regimes and the resulting steady-state cell shapes. It builds on previous studies that examined how spontaneous protrusions form under certain conditions. The current study seeks to extend these findings by analyzing the evolution of cell contours beyond the linear regime. This approach offers a new perspective on how cellular shapes emerge from the dynamic balance of internal and external forces.

Purpose Of The Study:

This study aims to investigate how cellular shapes arise from the interaction between protrusive and adhesive forces. The researchers focus on the feedback between membrane shape and the forces acting on it. They use a theoretical model to simulate the evolution of cell contours beyond the linear instability regime. The model incorporates curvature-sensitive membrane complexes that influence the shape of the cell. The study seeks to determine the final steady-state shapes that emerge from this dynamic process. It also aims to explain how the strength of protrusive forces affects the formation of protrusions. The researchers are particularly interested in how these forces lead to different morphologies, such as those seen in lamellipodia. By analyzing these patterns, the study hopes to provide a theoretical basis for understanding experimental observations of cell shape variability.

Main Methods:

The researchers developed a theoretical model to simulate the evolution of cell contours. The model incorporates forces from actin polymerization and adhesion to the extracellular matrix. It includes curvature-sensitive membrane complexes that influence the shape of the cell. The study builds on previous work that examined linear instability regimes. The current analysis extends beyond this regime to determine steady-state shapes. The model calculates the evolution of a two-dimensional cell contour over time. It uses computational methods to simulate the feedback between membrane shape and the forces acting on it. The researchers analyze the resulting shapes to identify patterns and their dependence on protrusive force strength.

Main Results:

The study found that shapes driven by adhesion or actin polymerization have distinct morphologies. These differences align with experimental observations of cellular structures. As protrusive forces decrease, the system stabilizes into a periodic pattern of protrusions. This result suggests a possible explanation for how cell shape depends on the extracellular matrix. The model shows that the strength of protrusive forces directly affects the final cell shape. The simulations reveal that lower protrusive forces lead to more regular protrusion patterns. The researchers observed that the model accurately captures the transition from unstable to stable shapes. These findings provide a theoretical framework for understanding the role of force dynamics in cell morphology.

Conclusions:

The authors propose that the model explains the emergence of distinct cell shapes from protrusive and adhesive forces. They suggest that the strength of protrusive forces influences the stability of protrusion patterns. The model supports the idea that curvature-sensitive membrane complexes play a role in shaping the cell. The findings align with experimental observations of cell shape variability. The researchers conclude that the model provides a theoretical basis for understanding how cell shape depends on the extracellular matrix. They propose that the model can help explain puzzling experimental results regarding shape changes. The study highlights the importance of feedback between membrane shape and force generation. The authors suggest that further research could explore the model's applicability to different cell types.

The model shows that cell shapes driven by adhesion or actin polymerization have distinct morphologies, as observed in cells.

The model suggests that the strength of protrusive forces affects the stabilization of protrusion patterns, which may explain shape dependence on the matrix.

The feedback mechanism allows the model to simulate how curvature-sensitive membrane complexes influence the evolution of cell contours.

These complexes mediate the feedback between membrane shape and the forces acting on it, influencing the final cell morphology.

As protrusive forces diminish, the system stabilizes into a periodic pattern of protrusions.

The authors propose that the model can provide an explanation for puzzling experimental results on cell shape dependence on the extracellular matrix.