Lamellipodia

Lamellipodia are broad, sheet-like protrusions at the leading edge of migrating cells that help direct movement across a substrate. They form when signaling pathways activate actin-nucleating factors, including the Arp2/3 complex, which generates a branched network of filamentous actin; continuous actin polymerization pushes the plasma membrane forward while adhesion complexes provide traction. Lamellipodia coordinate cell polarity, protrusion, and retraction during wound healing, embryonic development, immune-cell trafficking, and tissue remodeling. Their dynamics also influence cancer-cell invasion, making lamellipodia important for understanding cytoskeletal regulation and the cellular mechanisms that control migration.

Lamellipodia - Related Videos

Education

JoVE Core - Cell Biology

Mechanism of Lamellipodia Formation

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2023

Cells migrating in response to external stimuli form lamellipodia, which are thin membrane protrusions supported by a mesh of linked, branched, or unbranched actin filaments. These actin filaments interact with myosin motor proteins, creating the dynamic actomyosin complex within the cytoskeleton. Contractility, or the ability to generate contractile stress, is inherent to the actomyosin complex. It helps cells detect the stiffness of the surrounding ECM and exert contractile force for...

Research

JoVE EoE - Immunodiagnostics

The Photoconversion Technique for Exploring Inflammatory Cell Dynamics in Insect Pupae

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2025

The video demonstrates the use of photoconversion to study inflammatory cell dynamics in Drosophila pupae. Green hemocytes are drawn to the wounded epithelium, followed by distant migration. Photoconversion shifts certain hemocytes from green to red, facilitating their movement tracking.

In Vitro Assessment of Aggregated Amyloid-β on Neuronal Growth Cone Collapse

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2025

This video demonstrates an in vitro assessment of neuronal growth cone collapse by amyloid-β (Aβ) aggregates. Treating the neurons with Aβ aggregates causes cytoskeletal destabilization, leading to the collapse of growth cones at the tip of the axons. The treated cells are compared with control cells to assess the extent of growth cone collapse.

Wound Assay to Evaluate the Migratory Capacity of Murine Myoblasts in Co-Culture

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2025

This video describes a non-contact co-culture wound healing assay to evaluate the migratory capacity of murine myoblasts. This helps to understand signal-sending and signal-receiving components of the paracrine non-canonical Wnt signaling interactions in vitro.

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