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Related Concept Videos

Actin Filament Depolymerization01:19

Actin Filament Depolymerization

Actin filaments (F-actin) are composed of actin subunits. The dissociation of actin monomers can occur from either end of F-actin. The rate of dissociation is faster from the minus-end or the pointed end, where the actin subunits exist with a bound ADP, together known as ADP-actin. The depolymerization of F-actin is aided by proteins, including the actin-depolymerizing factor (ADF) and cofilin family of proteins, gelsolin, and glia maturation factor (GMF).
In F-actin, the ADF/cofilin proteins...
Mechanism of Filopodia Formation01:39

Mechanism of Filopodia Formation

Filopodia are thin, actin-rich cellular protrusions that play an important role in many fundamental cellular functions. They vary in their occurrence, length, and positioning in different cell types, suggesting their diverse roles.
Their main function is to guide migrating cells during normal tissue morphogenesis or cancer metastasis by recognizing and making initial contacts with the extracellular matrix. However, they can also act as stationary cell anchors or help to establish communication...
Cytoskeletal Coordination in Cell Migration01:32

Cytoskeletal Coordination in Cell Migration

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 proteins that...
Condensins02:15

Condensins

Condensins are large protein complexes that use ATP to fuel the assembly of chromosomes during mitosis. They transform the tangled, shapeless mass of post-interphase DNA into individualized chromosomes by compacting, organizing, and segregating chromosomal DNA.
The plant and animal cells contain two types of condensin complexes—condensin I and condensin II. Both complexes have five subunits: two SMC (Structural Maintenance of Chromosomes) subunits, a kleisin subunit, and two HEAT-repeat...
Mechanism of Lamellipodia Formation01:31

Mechanism of Lamellipodia Formation

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...
Generation of Straight or Branched Actin Filaments01:14

Generation of Straight or Branched Actin Filaments

The straight or branched structure formation of actin filaments is controlled by nucleating proteins such as the formins and Arp2/3 complex. Formin-mediated assembly results in straight filaments, whereas Arp2/3 protein complex-mediated assembly results in branched actin filaments.
Arp2/3 Complex
Arp2/3 complex is a seven-subunit complex consisting of two proteins similar to actin- Arp2 and Arp3, and five other subunits that help keep Arp2 and Arp3 inactive. When required, the complex is...

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Related Experiment Video

Updated: Jun 20, 2026

Aip1p Dynamics Are Altered by the R256H Mutation in Actin
08:57

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Published on: July 30, 2014

Decreased cofilin1 expression is important for compaction during early mouse embryo development.

Minyue Ma1, Lin Zhou, Xuejiang Guo

  • 1Laboratory of Reproductive Medicine, Department of Histology and Embryology, Nanjing Medical University, Nanjing 210029, China.

Biochimica Et Biophysica Acta
|September 16, 2009
PubMed
Summary

Cofilin1 down-regulation accelerates mouse embryo compaction by promoting cell flattening and polarity. Inactivation of cofilin1 is critical for establishing cellular asymmetry during early development.

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Area of Science:

  • Developmental Biology
  • Cell Biology
  • Molecular Biology

Background:

  • Early mouse development involves compaction, establishing cellular asymmetry through cell flattening and polarization.
  • The cytoskeletal mechanisms underlying polarized molecule and organelle distribution during compaction are not fully understood.

Purpose of the Study:

  • To investigate the role of cofilin1, an actin-binding protein, in mouse embryonic compaction.
  • To elucidate the cytoskeletal basis for cell polarity establishment during this critical developmental stage.

Main Methods:

  • RNA interference (siRNA) microinjection to down-regulate cofilin1 expression.
  • Time-lapse video microscopy for continuous observation of embryonic development.
  • Pronuclear microinjection of mutated cofilin1 plasmids.
  • Fluorescein-phalloidin staining and scanning electron microscopy.

Main Results:

  • Decreased cofilin1 expression accelerated compaction and promoted apical pole formation.
  • Microinjection of anti-cofilin1 antibody or siRNA led to earlier cell adherence.
  • Sustained active cofilin1 resulted in blastomeres that failed to adhere, indicating cofilin1 inactivation is crucial.
  • Cofilin1 knockdown embryos showed microvilli formation on blastomeres.

Conclusions:

  • Cofilin1 plays a significant role in regulating cortical cytoplasmic organization during mouse embryo compaction.
  • Cofilin1 inactivation is essential for cell flattening, adherence, and polarity establishment.
  • These findings highlight cofilin1's importance in the cytoskeletal dynamics governing early embryonic development.