Gap junction

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Overview

A gap junction or nexus is a junction between certain animal cell-types that allows different molecules and ions, mostly small intracellular signaling molecules (intracellular mediators), to pass freely between cells. The junction connects the cytoplasm of cells. One gap junction is composed of two connexons (or hemichannels) which connect across the intercellular space. They are analogous to the plasmodesmata that join plant cells^[1].

Structure

In vertebrates, gap junction hemichannels are primarily homo- or hetero-hexamers of connexin proteins. Invertebrate gap junctions comprise proteins from the hypothetical innexin family. However, the recently characterized pannexin family, functionally similar but genetically distinct from connexins and expressed in both vertebrates and invertebrates, probably encompasses the innexins.

At gap junctions, the intercellular spaces narrows from 25nm to 3nm and unit connexons in the membrane of each cell are lined up with one another.

Gap junctions formed from two identical hemichannels are called homotypic, while those with differing hemichannels are heterotypic. In turn, hemichannels of uniform connexin composition are called homomeric, while those with differing connexins are heteromeric. Channel composition is thought to influence the function of gap junction channels but it is not yet known how.

Generally, the genes coding for gap junctions are classified in one of three groups, based on sequence similarity: A, B and C (for example, GJA1, GJC1). However, genes do not code directly for the expression of gap junctions; genes can only produce the proteins which make up gap junctions (connexins). An alternative naming system based on this protein's molecular weight is also popular (for example: connexin43, connexin30.3).

Levels of organization

1. DNA to RNA to Connexin protein.
2. One connexin protein has four transmembrane domains
3. 6 Connexins create one Connexon (hemichannel). When different connexins join together to form one connexon, it is called a heteromeric connexon
4. Two hemichannels, joined together across a cell membrane comprise a Gap Junction.

When two identical connexons come together to form a Gap junction, it is called a homotypic GJ. When one homomeric connexon and one heteromeric connexon come together, it is called a heterotypic gap junction. When two heteromeric connexons join, it is also called a heteromeric Gap Junction.

1. Several gap junctions (hundreds) assemble into a macromolecular complex called a plaque.

Properties

1. Allows for direct electrical communication between cells, although different connexin subunits can impart different single channel conductances, from about 30 pS to 500 pS.
2. Allows for chemical communication between cells, through the transmission of small second messengers, such as IP₃ and Ca^2+[1], although different connexin subunits can impart different selectivity for particular small molecules.
3. Generally allows molecules smaller than 1,000 Daltons to pass through, although different connexin subunits can impart different pore sizes and different charge selectivity. Large biomolecules, for example, nucleic acid and protein, are not allowed to be shared.

Areas of electrical coupling

Heart

Gap junctions are particularly important in the cardiac muscle: the signal to contract is passed efficiently through the gap junctions, allowing the heart muscle cells to contract in tandem. However, gap junctions are now known to be expressed in virtually all tissues of the body, with the exception of mobile cell types such as sperm or erythrocytes. Several human genetic disorders are now associated with mutations in gap junction genes. Many of those affect the skin, because this tissue is heavily dependent upon gap junction communication for the regulation of differentiation and proliferation.

Neurons

Few locations have been discovered where there is siginificant coupling between neurons in the brain. Structures in the brain that have been shown to contain electrically coupled neurons include the vestibular nucleus, the nucleus of trigeminal nerve, the inferior olivary nucleus, and the Ventral Tegmental Area. There has been some observation of weak neuron to glial cell coupling in the locus coeruleus, and in the cerebellum between Purkinje neurons and Bergmann glial cells. It now seems that astrocytes are strongly coupled by gap junctions. Experimental data show strong gap junction expression in astrocytes. Moreover, mutations in the gap junction genes Cx43 and Cx56.6 cause white matter degeneration similar to that observed in Pelizaeus-Merzbacher disease and multiple sclerosis.

Connexin proteins expressed in neurons include:

1. mCX26
2. mCX43
3. mCX36
4. mCX56.6
5. mCX57
6. mCX45

Retina

Neurons within the retina show extensive coupling, both within populations of one cell type, and between different cell types.

See also

• Electrical synapse
• Ion channel
• Junctional complex
• Intercalated disc
• Cardiac muscle
• Tight junction
• Desmosomes

References

External links

• MeSH Gap+Junctions

v • d • e Histology: epithelial tissue
Types	Columnar (simple, stratified) - Cuboidal (simple, stratified) - Pseudostratified - Respiratory - Squamous (simple, stratified) - Transitional - Olfactory
Features	Lateral/cell-cell: Tight junction - Adherens junction - Desmosome - Gap junction Basal/cell-matrix: Basal lamina - Hemidesmosome - Focal adhesion Apical: Cilia - Microvilli - Stereocilia

de:Gap junction

fr:Jonction communicante hr:Gap junction ja:ギャップ結合 fi:Aukkoliitos sv:Gap junction

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