Adherens junction

Principal interactions of structural proteins at cadherin-based adherens junction. Actin filaments are associated with adherens junctions in addition to several other actin-binding proteins such as vinculin. The head domain of vinculin associates to E-cadherin via α-, β - and γ -catenins. The tail domain of vinculin binds to membrane lipids and to actin filaments.

Adherens junctions (or zonula adherens) are protein complexes that occur at cell-cell junctions in epithelial tissues, usually more basal than tight junctions. An adherens junction is defined as a cell junction whose cytoplasmic face is linked to the actin cytoskeleton. They can appear as bands encircling the cell (zonula adherens) or as spots of attachment to the extracellular matrix (adhesion plaques).

A similar cell junction in non-epithelial cells is the fascia adherens. It is structurally the same, but appears in ribbonlike patterns that do not completely encircle the cells. One example is in cardiomyocytes.

Proteins

Adherens junctions are composed of the following proteins:

• cadherins. The cadherins are a family of transmembrane proteins that form homodimers in a calcium-dependent manner with other cadherin molecules on adjacent cells.
• p120 (sometimes called delta catenin) binds the juxtamembrane region of the cadherin.
• β-catenin or gamma-catenin (plakoglobin) binds the catenin-binding region of the cadherin.
• α-catenin binds the cadherin indirectly via β-catenin or plakoglobin.

^[1]

Models

Adherens junctions were, for many years, thought to share the characteristic of anchor cells through their cytoplasmic actin filaments.

The accepted model has been that adherens junctions serve as a bridge connecting the actin cytoskeleton of neighboring cells through direct interaction. However, scientists have not been able to isolate the quaternary complex of cadherin-βcatenin-αcatenin-actin in vitro. Recent data (2005) from 2 labs at Stanford University published in the journal Cell demonstrates that membrane associated actin is several fold less stable compared to components of the adherens junctional complex.^[2][3]

Additionally, the authors found that monomeric α-catenin preferentially binds to the cadherin junction complex through β-catenin. Dimeric α-catenin preferentially binds to actin and suppresses Arp2/3 complex-mediated actin branching, thus acting as a molecular switch to regulate actin polymerization.

Adherens junctions may serve as a regulatory module to maintain the actin contractile ring with which it is associated in microscopic studies.

References

External links

• MeSH Adherens+Junctions
• Histology at BU 20502loa

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