Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Membrane Domains01:18

Membrane Domains

The membrane domains concentrate specific lipids and proteins at one place within the membrane, which helps in cell signaling, adhesion, and other critical cellular processes. These domains can differ in size, composition, function, and lifespan.
Protein Domains
The membrane comprises a group of distinct proteins responsible for carrying out a cell's specific function. For example, the plasma membrane of the human sperm, or a single germ cell, contains a unique set of proteins in the anterior...
Mechanisms of Membrane Domain Formation00:59

Mechanisms of Membrane Domain Formation

Different physical properties of lipids and proteins allow them to localize and form distinct islands or domains in the membrane. Some membrane domains are formed due to protein-protein interactions, whereas others are formed due to the presence of specific lipids such as sphingolipids and sterols—for example, large proteins, such as bacteriorhodopsin, aggregate and create distinct domains.
Another mechanism for membrane domain formation involves membrane proteins interacting with cytoskeletal...
Intracellular Signaling Affects Focal Adhesions01:17

Intracellular Signaling Affects Focal Adhesions

Integrins act both as extracellular input receivers and as intracellular processing activators. As their name suggests, integrins are entirely integrated into the membrane structure. Their hydrophobic membrane-spanning regions interact with the phospholipid bilayer's hydrophobic region. These membrane receptors provide extracellular attachment sites for effectors like hormones and growth factors. They activate intracellular response cascades when their effectors are bound and active.
Some...
Fluid Mosaic Model01:19

Fluid Mosaic Model

Scientists identified the plasma membrane in the 1890s and its principal chemical components (lipids and proteins) by 1915. The model for plasma membrane structure, proposed in 1935 by Hugh Davson and James Danielli, was the first model to be widely accepted in the scientific community. The model was based on the plasma membrane's "railroad track" appearance in early electron micrographs. Davson and Danielli theorized that the plasma membrane's structure resembled a sandwich with the analogy of...
Immunoglobulin-like Cell Adhesion Molecules01:31

Immunoglobulin-like Cell Adhesion Molecules

Immunoglobulin-like cell adhesion molecules or Ig-CAMs are a versatile group of cell surface glycoproteins belonging to the immunoglobulin protein superfamily. Ig-CAMs possess the characteristic immunoglobulin protein domains and other domains such as the fibronectin type III domain. The Ig domains are glycosylated to varying degrees in different Ig-CAMs.
Ig-CAMs exhibit either homophilic binding (to other Ig-CAMs) or heterophilic binding (to other ligands such as integrins). While most Ig-CAMs...
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...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Nuclear transport of human cytomegalovirus tegument protein pp65 through nucleoplasmic reticulum.

PLoS pathogens·2026
Same author

Extracellular vesicles and viruses share a nuclear entry pathway in cancer and infection.

Frontiers in cell and developmental biology·2026
Same author

Physical exercise increases binding of POMC to blood extracellular vesicles.

Proceedings of the National Academy of Sciences of the United States of America·2025
Same author

Correction: The primary cilium as a multifunctional organelle: emerging roles and unanswered questions.

Cell communication and signaling : CCS·2025
Same author

The primary cilium as a multifunctional organelle: emerging roles and unanswered questions.

Cell communication and signaling : CCS·2025
Same author

Extracellular membrane particles en route to the nucleus - exploring the VOR complex.

Biochemical Society transactions·2025

Related Experiment Video

Updated: May 28, 2026

Single-Molecule Localization Microscopy of Membrane Proteins using Single-Antibody Labeling
07:51

Single-Molecule Localization Microscopy of Membrane Proteins using Single-Antibody Labeling

Published on: March 20, 2026

CD133 and membrane microdomains: old facets for future hypotheses.

Christine A Fargeas, Jana Karbanová, József Jászai

    World Journal of Gastroenterology
    |November 1, 2011
    PubMed
    Summary

    Investigating membrane microdomains in digestive tract cells, particularly CD133 (prominin-1), reveals insights into cell organization and cancer stem cell targeting. This research enhances understanding of cellular transformation and offers diagnostic potential.

    Keywords:
    AC133CD133CancerMembrane microdomainsMembrane vesiclesProminin-1Stem cell

    More Related Videos

    Nanopodia - Thin, Fragile Membrane Projections with Roles in Cell Movement and Intercellular Interactions
    10:50

    Nanopodia - Thin, Fragile Membrane Projections with Roles in Cell Movement and Intercellular Interactions

    Published on: April 3, 2014

    An Endothelial Planar Cell Model for Imaging Immunological Synapse Dynamics
    09:25

    An Endothelial Planar Cell Model for Imaging Immunological Synapse Dynamics

    Published on: December 24, 2015

    Related Experiment Videos

    Last Updated: May 28, 2026

    Single-Molecule Localization Microscopy of Membrane Proteins using Single-Antibody Labeling
    07:51

    Single-Molecule Localization Microscopy of Membrane Proteins using Single-Antibody Labeling

    Published on: March 20, 2026

    Nanopodia - Thin, Fragile Membrane Projections with Roles in Cell Movement and Intercellular Interactions
    10:50

    Nanopodia - Thin, Fragile Membrane Projections with Roles in Cell Movement and Intercellular Interactions

    Published on: April 3, 2014

    An Endothelial Planar Cell Model for Imaging Immunological Synapse Dynamics
    09:25

    An Endothelial Planar Cell Model for Imaging Immunological Synapse Dynamics

    Published on: December 24, 2015

    Area of Science:

    • Cell Biology
    • Cancer Research
    • Gastroenterology

    Background:

    • Membrane microdomains are crucial for normal and cancerous digestive tract cells.
    • Understanding their organization is vital for basic science and clinical applications.
    • The molecule CD133 (prominin-1) is a key focus in studying these microdomains.

    Discussion:

    • CD133's association with specific membrane microdomains impacts polarized epithelial cell dynamics.
    • This association is relevant in both normal cellular functions and cancer stem cell biology.
    • Exploring these interactions provides insights into cellular transformation processes.

    Key Insights:

    • Novel aspects of polarized epithelial cell organization and dynamics have been uncovered.
    • CD133's role in membrane microdomains is central to these findings.
    • The study highlights the significance of microdomain organization in cellular transformation.

    Outlook:

    • Findings may lead to new diagnostic methods for digestive tract cancers.
    • Targeting cancer stem cells via CD133-associated microdomains is a promising therapeutic avenue.
    • Further research into microdomain function can advance cancer stem cell biology.