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Membrane-enclosed structures called vesicles transport proteins and lipids across the cell. The vesicles derive their cargo from the plasma membrane, Golgi, ER, or endosome. Coated vesicles are spherical, protein-coated carriers with a 50–100 nm diameter that mediate bidirectional transport between the ER and the Golgi. The distribution of proteins between the ER and Golgi complex is dynamic and is maintained by different coated vesicles. Their formation is driven by the assembly of...
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Clathrin-coated vesicles use endocytosis to transport receptors and lysosomal hydrolases from the Golgi to the lysosome in the late secretory pathway. Clathrin-mediated endocytosis was the first described endocytic process, and Clathrin-coated vesicles remain one of the most well-studied transport vesicles. The molecular machinery that generates clathrin-coated vesicles comprises over 50 proteins that precisely coordinate vesicle formation. Cell surface receptors concentrated in indented sites...
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Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...
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Eukaryotic cells use different mechanisms to eliminate toxic waste obsolete and worn-out substances. Lysosomes play a pivotal role in this, and hence, these substances are carried to the lysosome from other parts of the cell and extracellular space through different pathways. The most elaborately studied pathways to the lysosome are the endocytic pathways.
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Phagocytosis00:41

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Cells pull particles inward and engulf them in spherical vesicles in an energy-requiring process called endocytosis. Phagocytosis ("cellular eating") is one of three major types of endocytosis. Cells use phagocytosis to take in large objects, such as other cells (or their debris), bacteria, and even viruses.
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Cells pull particles inward and engulf them in spherical vesicles in an energy-requiring process called endocytosis. Phagocytosis (“cellular eating”) is one of three major types of endocytosis. Cells use phagocytosis to take in large objects—such as other cells (or their debris), bacteria, and even viruses.
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Related Experiment Video

Updated: Feb 18, 2026

Author Spotlight: Tackling Challenges in Synthetic Cell Engineering
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How gluttonous cell aggregates clear substrates coated with microparticles.

Grégory Beaune1, Andy Y W Lam1, Sylvie Dufour2,3

  • 1WPI International Center for Materials Nanoarchitectonics (MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki, 305-0044, Japan.

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Cell aggregates spread on microparticle-decorated substrates, with peripheral cells internalizing microparticles (MPs). This process quantifies cell-particle internalization, offering a simple measurement method.

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Area of Science:

  • Cell biology
  • Biophysics
  • Materials science

Background:

  • Cell aggregates exhibit spreading behavior on substrates.
  • Microparticles (MPs) on substrates are encountered during cell migration.
  • Understanding cell-substrate interactions is crucial for biological and material applications.

Purpose of the Study:

  • To investigate the dynamics of cell aggregate spreading on microparticle-decorated substrates.
  • To analyze the internalization of microparticles by migrating cells.
  • To develop a method for quantifying cell-particle internalization.

Main Methods:

  • Depositing cell aggregates on adhesive substrates with microparticles.
  • Observing and measuring the spreading of the cell monolayer.
  • Analyzing the formation and characteristics of the cell-filled aureole.
  • Quantifying microparticle uptake based on aureole dimensions.

Main Results:

  • Cell monolayers expand around aggregates, internalizing microparticles.
  • The width of the cell-filled aureole and MP internalization depend on MP size, composition, and density.
  • Aureole radius and width measurements allow quantification of cell-particle internalization volume fraction.

Conclusions:

  • Cell spreading on microparticle-laden substrates leads to microparticle internalization.
  • The study provides a straightforward, rapid, and cost-effective method for measuring cell-particle internalization.
  • This method can be applied to assess cell-particle interactions in various contexts.