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

Structure of Cadherins01:25

Structure of Cadherins

4.9K
The cadherins were one of the first cell adhesion molecules discovered; the term “cadherins”   is based on their calcium-dependent adhering properties. The first cadherins discovered on the epithelial, neuronal, and placental cells were named E-cadherin, P-cadherin, and N-cadherin, respectively. These classical cadherins share sequence and structural similarities. Other cadherins, including those involved in cell signaling, are grouped into non-classical cadherins. This...
4.9K
Cadherins in Tissue Organization01:19

Cadherins in Tissue Organization

4.3K
The cadherins are a superfamily of cell adhesion molecules comprising over 180 variants, with specific tissues expressing a particular combination of cadherin types. Cadherins generally exhibit homophilic binding; i.e., cadherins on one cell bind to cadherins of the same or closely related type on another cell. Thus, cells of the same type have a specific affinity to bind to each other and sort themselves into clusters to form tissues.
Cell Sorting During Development
Cell sorting plays an...
4.3K
Catenins01:23

Catenins

3.1K
Catenins are characterized by multiple binding domains and dynamic structures that allow them to function as linker proteins in cell junction complexes. All catenins, except α-catenin, contain a characteristic protein sequence called the armadillo repeat and are therefore also called armadillo proteins.
Catenins in Cell Junctions
Catenins bind to cell adhesion molecules such as cadherins and link them to different cytoskeletal proteins depending on the type of cell junction. At the...
3.1K
Desmosomes01:05

Desmosomes

7.9K
The term desmosome derives from the Greek words "desmo" and "soma" meaning "adhesion bodies." This structure was first observed during the late 1800s and described as small, dense nodules in the epidermis. Desmosomes are button-like structures that help form an interlinked network of intermediate filaments across the cells. These junctions are  essential to hold cells together under mechanical stress and to maintain tissue integrity. Desmosomes are multi-protein...
7.9K
Cell Adhesion Molecules - Types and Functions01:20

Cell Adhesion Molecules - Types and Functions

9.9K
Cell adhesion molecules (CAMs) are pivotal to multicellularity and the coordinated functioning of tissues and organ systems. They enable physical interactions between cells and provide mechanical strength to tissues. They also function as receptors for signal transmission across the plasma membrane. The CAMs are broadly classified into four families - integrins, cadherins, selectins, and immunoglobulin-like CAMs (IgCAMs).
CAM Families
The Integrin family of proteins is primarily  involved...
9.9K
Adherens Junctions01:24

Adherens Junctions

6.6K
Strong contact points between adjacent cells anchor them to each other, forming tissues. Such anchoring junctions are of two types –  adherens junctions and desmosomes. Adherens junctions are abundant in tissues such as  epithelium and endothelium, forming a continuous zone of adhesion called the adhesion belt. In other tissues, such as  heart muscle, they appear as clusters, linking the cells to produce coordinated heart muscle contraction.
Adherens Junctions are Dynamic
6.6K

You might also read

Related Articles

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

Sort by
Same author

The Nemp1-Nesprin complex mediates cellular responses to matrix mechanics.

Proceedings of the National Academy of Sciences of the United States of America·2026
Same author

Nuclear Envelope Membrane Protein 1 plays crucial and conserved roles in female meiosis.

Research square·2025
Same author

Fat cadherin cleavage releases a transcriptionally active nuclear fragment to regulate target gene expression.

bioRxiv : the preprint server for biology·2025
Same author

Regulation of Hippo signaling and planar cell polarity via distinct regions of the Fat intracellular domain.

Development (Cambridge, England)·2025
Same author

Gastric hypoplasia in mice lacking fibroblast growth factor 9.

Developmental dynamics : an official publication of the American Association of Anatomists·2025
Same author

SOX9 Governs Gastric Mucous Neck Cell Identity and Is Required for Injury-Induced Metaplasia.

Cellular and molecular gastroenterology and hepatology·2023

Related Experiment Video

Updated: Feb 16, 2026

Bead Aggregation Assays for the Characterization of Putative Cell Adhesion Molecules
08:15

Bead Aggregation Assays for the Characterization of Putative Cell Adhesion Molecules

Published on: October 17, 2014

11.0K

Big roles for Fat cadherins.

Seth Blair1, Helen McNeill2

  • 1Department of Integrative Biology, University of Wisconsin, Madison, USA.

Current Opinion in Cell Biology
|December 20, 2017
PubMed
Summary

This study explores how two large cell adhesion proteins, Fat and Dachsous, regulate organ development. These proteins coordinate multiple cellular processes like cell elongation, migration, and metabolism. They act as a ligand-receptor system, influencing downstream signaling pathways. The research highlights gaps in understanding how these proteins function. Their interaction with the Hippo pathway suggests a broader regulatory role. The findings suggest that Fat and Dachsous are master regulators of tissue patterning. Further research is needed to clarify their exact mechanisms and interactions.

Keywords:
Fat cadherinsDachsous signalingorgan developmentcell adhesion

Frequently Asked Questions

More Related Videos

Immunomagnetic Separation of Fat Depot-specific Sca1high Adipose-derived Stem Cells ASCs
08:52

Immunomagnetic Separation of Fat Depot-specific Sca1high Adipose-derived Stem Cells ASCs

Published on: August 11, 2016

7.4K
Modeling Paracrine Noncanonical Wnt Signaling In Vitro
11:14

Modeling Paracrine Noncanonical Wnt Signaling In Vitro

Published on: December 10, 2021

1.9K

Related Experiment Videos

Last Updated: Feb 16, 2026

Bead Aggregation Assays for the Characterization of Putative Cell Adhesion Molecules
08:15

Bead Aggregation Assays for the Characterization of Putative Cell Adhesion Molecules

Published on: October 17, 2014

11.0K
Immunomagnetic Separation of Fat Depot-specific Sca1high Adipose-derived Stem Cells ASCs
08:52

Immunomagnetic Separation of Fat Depot-specific Sca1high Adipose-derived Stem Cells ASCs

Published on: August 11, 2016

7.4K
Modeling Paracrine Noncanonical Wnt Signaling In Vitro
11:14

Modeling Paracrine Noncanonical Wnt Signaling In Vitro

Published on: December 10, 2021

1.9K

Area of Science:

  • Developmental biology
  • Cell adhesion mechanisms
  • Molecular signaling pathways

Background:

Organ formation requires precise coordination of multiple cellular activities. While individual processes like cell elongation and adhesion are well understood, their synchronized regulation remains unclear. Prior research has shown that cell adhesion molecules influence tissue patterning. However, how these molecules coordinate multiple processes is less clear. This gap motivated investigation into specific adhesion systems. No prior work had resolved how large adhesion proteins might regulate diverse functions. The Fat and Dachsous proteins are known to interact, but their exact roles remain uncertain. That uncertainty drove recent studies into their signaling mechanisms. Understanding these interactions could clarify how organs achieve consistent shape and size.

Purpose Of The Study:

The study aimed to explore how Fat and Dachsous proteins regulate organ development. These proteins are large and function as a ligand-receptor pair. Their role in cell adhesion is established, but their broader influence is unclear. The researchers sought to understand how these proteins coordinate multiple cellular processes. They focused on mechanisms like cell migration and polarization. The goal was to identify how these proteins integrate signals across tissues. Their work aimed to clarify the signaling pathways involved. This study aimed to bridge the gap between adhesion and organ patterning.

Main Methods:

The researchers reviewed recent findings on the Ds-Ft pathway. They analyzed how these proteins interact with other signaling components. They examined data from various model systems to identify common patterns. They focused on how these proteins affect cell shape and movement. The team used genetic and biochemical approaches to map interactions. They compared results from different developmental stages. The study combined computational modeling with experimental data. The approach aimed to reveal how these proteins coordinate multiple functions.

Main Results:

The Ds-Ft pathway influences cell elongation and migration. It also regulates cell metabolism and proliferation rates. These proteins affect planar polarization and junctional contractions. The pathway coordinates diverse processes across tissues. The study found that Ds and Ft act as a ligand-receptor system. Their interaction modulates signaling through downstream effectors. The proteins influence Hippo signaling and other pathways. These findings suggest a central role for Ds-Ft in organ development.

Conclusions:

The Ds-Ft pathway regulates multiple cellular processes during development. These proteins coordinate adhesion, polarization, and metabolism. Their interaction suggests a broader signaling role than previously thought. The study highlights gaps in understanding how these proteins function. The findings suggest that Ds-Ft integrates signals across tissues. The authors propose that these proteins act as master regulators. Further research is needed to clarify their exact mechanisms. The study emphasizes the need for more detailed functional analysis.

According to the authors, Fat and Dachsous proteins regulate cell elongation, migration, and polarization through a ligand-receptor system. Their interaction modulates downstream signaling pathways.

The Ds-Ft pathway influences cell adhesion, metabolism, and proliferation. It coordinates diverse processes to ensure consistent organ shape and size.

The Ds-Ft pathway interacts with the Hippo signaling pathway. This connection suggests a broader regulatory role for these adhesion proteins.

The authors highlight that how Ds-Ft proteins regulate multiple processes remains unclear. Their exact mechanisms and interactions are still being studied.

The Ds-Ft pathway influences junctional contractions. This effect contributes to tissue patterning and organ shape.

Planar polarization is regulated by the Ds-Ft pathway. This process ensures coordinated cell movement and tissue organization.