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Desmosomes
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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...
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Anchoring Junctions
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Anchoring junctions are multiprotein complexes that help cells connect to other cells and the extracellular matrix. Anchoring junctions are present on the lateral and basal surfaces of cells, providing strong and flexible connections. Focal adhesions are often formed due to cell interactions with the ECM substrata, which initiate signal transduction via kinase cascades and other mechanisms. Together, they provide stability and tissue integrity. There are three types of anchoring junctions:...
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Assembly of Complex Microtubule Structures
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Complex microtubule structures are present in resting cells and in dividing cells. In resting cells, they are responsible for maintaining the cellular architecture, tracks for intracellular transport, positioning of organelles, assembly of cilia and flagella. They mediate the bipolar spindle assembly for chromosomal segregation and positioning of the cell division plate in dividing cells. The formation of microtubule complex structures depends on the cell type, cell stage, and cell function.
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Tension Response at Adherens Junctions
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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.
α-Catenin as a Mechanosensory Protein
The α-catenin of adherens junctions is an allosteric protein with three VH (vinculin...
α-Catenin as a Mechanosensory Protein
The α-catenin of adherens junctions is an allosteric protein with three VH (vinculin...
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Cell-matrix's Response to Mechanical Forces
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In animal cells, the extracellular matrix allows cells within tissues to withstand external stresses and transmits signals from the outside of the cell to the inside. The extracellular matrix is extensive, and its composition varies between different types of tissues. For example, the reticular fibers and ground substance make up the ECM in loose connective tissue, while collagen and bone minerals make up the ECM of bone tissue.
Anchoring junctions mechanically attach a cell to the...
Anchoring junctions mechanically attach a cell to the...
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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.
Adherens Junctions are Dynamic
Adherens Junctions are Dynamic
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Desmosomes undergo dynamic architectural changes during assembly and maturation.
Reena R Beggs1, Tejeshwar C Rao1, William F Dean1
1Department of Cell, Developmental, and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Tissue Barriers
|January 5, 2022
Summary
Desmosome assembly involves changes in desmoplakin architecture, impacting cell adhesion. These structural shifts during desmosome maturation are key to tissue integrity and mechanical strength.
Area of Science:
- Cell Biology
- Biophysics
- Epithelial Biology
Background:
- Desmosomes are crucial cell-cell junctions for tissue adhesion and mechanical stress resistance.
- The nanoscale organization and maturation process of desmosomes remain poorly understood.
Purpose of the Study:
- To investigate the relationship between desmosome molecular architecture and maturation.
- To quantify nanoscale changes during desmosome assembly and identify architectural markers of maturity.
Main Methods:
- Utilized a calcium switch assay to synchronize desmosome assembly.
- Employed direct Stochastic Optical Reconstruction Microscopy (dSTORM) for nanoscale imaging.
- Analyzed desmoplakin and plakoglobin organization and E-cadherin distribution.
Main Results:
- Desmoplakin rod/C-terminal organization changed with maturation (decreased plaque-to-plaque distance, increased length).
- Desmoplakin N-terminal and plakoglobin organization remained constant.
- Desmosome maturation correlated with E-cadherin exclusion and increased adhesion strength.
- Architectural changes were observed in cell migration models and across different epithelial cell types.
Conclusions:
- Desmosome maturation involves specific architectural rearrangements, particularly in desmoplakin.
- Desmosome nanoscale organization can serve as an indicator of maturation state.
- Desmoplakin architecture may play a role in regulating desmosome adhesive strength.


