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Related Concept Videos

Cytoskeletal Coordination in Cell Migration01:32

Cytoskeletal Coordination in Cell Migration

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A migrating cell changes its shape during the cyclic events of attachment and detachment from the substratum and repositions the cell organelles correspondingly. These complex events are orchestrated by the dynamic cytoskeletal network comprising actin filaments, intermediate filaments, and microtubules. Cytoskeletal crosstalk — the direct and indirect communication between the different components — is crucial for this coordination. Direct communication involves various linker...
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Cell Migration01:19

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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.
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Cell Migration01:09

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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.
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Role of Myosin in Cell Migration01:18

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Myosins are multimeric motor proteins involved in various cellular processes such as migration, adhesion, and proliferation. Myosin II is the most common type in animal cells, which binds and cross-links actin filaments.
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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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Cells can detect chemical cues in their environment and reorganize the cytoskeleton to migrate toward them or away from them. This directional migration, called chemotaxis, is essential during embryogenesis and development, immune response, tissue repair and regeneration, and reproduction. These chemical cues can either attract or repel the cell's movement. For example, axon development is determined by a combination of chemoattractants and chemorepellents that direct the growing axon...
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Traction Microscopy Integrated with Microfluidics for Chemotactic Collective Migration
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Mapping forces and kinematics during collective cell migration.

Xavier Serra-Picamal1, Vito Conte1, Raimon Sunyer1

  • 1Institute for Bioengineering of Catalonia, Barcelona, Spain.

Methods in Cell Biology
|February 3, 2015
PubMed
Summary
This summary is machine-generated.

Understanding collective cell migration is key for tissue repair and development. New techniques now allow precise measurement of cell forces and movements, advancing research in health and disease.

Keywords:
Collective cell migrationMonolayer stress microscopyTraction force microscopy

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Related Experiment Videos

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Area of Science:

  • Cell Biology
  • Biophysics
  • Developmental Biology

Background:

  • Collective cell migration is essential for fundamental biological processes like morphogenesis and tissue repair.
  • Epithelial and endothelial cells migrate cooperatively, relying on intercellular junctions.
  • Cellular movement involves forces exerted on the substrate (cell-substrate forces) and neighboring cells (cell-cell forces).

Purpose of the Study:

  • To describe quantitative techniques for measuring multicellular forces and kinematics.
  • To detail experimental protocols for these measurements.
  • To highlight the potential of these methods for understanding collective cell migration.

Main Methods:

  • Particle image velocimetry (PIV) for mapping cell velocities.
  • Traction force microscopy (TFM) for mapping cell-substrate forces.
  • Monolayer stress microscopy (MSM) for mapping intracellular and intercellular forces.

Main Results:

  • Recent advancements enable quantitative measurements of multicellular forces and kinematics at high resolution.
  • Specific techniques like PIV, TFM, and MSM allow detailed mapping of cell movement and forces.
  • Experimental protocols for these measurements are described.

Conclusions:

  • The described techniques provide unprecedented resolution for studying collective cell migration.
  • Combining these methods with advanced imaging and molecular perturbations will deepen our understanding of migration mechanisms.
  • This research is crucial for advancing knowledge in both normal biological processes and disease states.