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Related Concept Videos

Cadherins in Tissue Organization01:19

Cadherins in Tissue Organization

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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
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Cell Migration01:19

Cell Migration

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Cell migration is a process by which the cells move from one location to another, playing an essential role in embryological development, repair and regeneration, immune response, and metastasis. Cells migrate in response to chemical or mechanical signals generated by specific organs or tissues. The overall mechanism includes three steps - polarization, protrusion, and release. Polarization involves the formation of a distinct cell front and rear, which determines the direction of movement.
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Cell Adhesion in Plants01:14

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Plants have rigid cell walls that are made up of cell wall polysaccharides that mediate cell-cell adhesion. The primary cell walls of plants consist of two independent and interacting polysaccharide networks: a pectin matrix that embeds the second network comprising cellulose and hemicelluloses.
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Adherens Junctions01:24

Adherens Junctions

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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.
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Tension Response at Adherens Junctions01:26

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The adherens junctions that anchor cells together are multi-protein complexes that dynamically adapt to mechanical stimuli such as tensile forces and shear stress. Mechanosensory proteins in these junctions can sense such mechanical stimuli and undergo a shift in their conformation, resulting in an altered function — a process called mechanotransduction.
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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...
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Mapping the Emergent Spatial Organization of Mammalian Cells using Micropatterns and Quantitative Imaging
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Adhesion-Based Self-Organization in Tissue Patterning.

Tony Y-C Tsai1, Rikki M Garner2, Sean G Megason2

  • 1Department of Developmental Biology, Washington University School of Medicine, St. Louis, Missouri, USA;

Annual Review of Cell and Developmental Biology
|May 14, 2022
PubMed
Summary
This summary is machine-generated.

Cell adhesion and cortical tension drive tissue patterning during development. New research integrates theoretical and experimental methods to understand these complex cellular dynamics for developmental biology insights.

Keywords:
cell adhesioncell sortingdevelopmental biologyinterfacial tensiontissue patterning

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Area of Science:

  • Developmental Biology
  • Cell Biology
  • Biophysics

Background:

  • The differential adhesion hypothesis explains how cell adhesion mediates self-organization and spatial pattern formation during development.
  • Historically, research focused on homophilic binding specificities of adhesion molecules.
  • Recent findings highlight the critical role of cortical tension and the signaling functions of adhesion proteins in regulating actomyosin contractility, shifting research focus.

Purpose of the Study:

  • To explore the shift in focus from simple adhesion binding to the signaling roles of adhesion proteins in regulating cellular dynamics.
  • To integrate theoretical and experimental approaches for a comprehensive understanding of adhesion-based tissue patterning.
  • To investigate the interplay between morphogen signaling, cell fate, and adhesion changes in robust patterning.

Main Methods:

  • Review and synthesis of current theoretical and experimental approaches in cell adhesion and tissue patterning research.
  • Analysis of the role of differential interfacial tension, encompassing both adhesion and nonadhesion molecules.
  • Examination of the coordination between signaling pathways, cell fate determination, and adhesion dynamics.

Main Results:

  • Adhesion molecules' signaling function in regulating actomyosin contractility is now central to differential adhesion studies.
  • The concept of differential interfacial tension provides a broader framework, unifying adhesion and nonadhesion molecules.
  • Effective tissue patterning relies on the coordinated interplay of morphogen signaling, cell fate decisions, and adhesion modulation.

Conclusions:

  • Understanding cell adhesion in development requires considering its role in regulating cortical tension and actomyosin contractility.
  • Integrating diverse molecular and cellular dynamics across multiple scales is crucial for deciphering adhesion-based tissue patterning.
  • Advances in theoretical and experimental methods offer new avenues for studying developmental self-organization.