Integrin beta 4: Difference between revisions
CSV import Tags: mobile edit mobile web edit |
CSV import |
||
| Line 1: | Line 1: | ||
{{Infobox protein | |||
| name = Integrin beta-4 | |||
| image = <!-- Image removed --> | |||
| width = | |||
| caption = | |||
| symbol = ITGB4 | |||
| HGNCid = 6158 | |||
| OMIM = 147557 | |||
| PDB = | |||
| RefSeq = NM_000213 | |||
| UniProt = P16144 | |||
| chromosomal_location = 17q25 | |||
}} | |||
'''Integrin beta-4''' (ITGB4) is a protein that in humans is encoded by the [[ITGB4]] gene. Integrins are [[transmembrane receptors]] that facilitate cell-extracellular matrix (ECM) adhesion. They are heterodimeric proteins consisting of alpha and beta subunits. The beta-4 subunit is unique in that it pairs with the alpha-6 subunit to form the [[α6β4 integrin]], which is primarily expressed in [[epithelial cells]]. | |||
Integrin beta 4 is a | |||
== Function == | == Function == | ||
Integrin beta 4 | Integrin beta-4 plays a critical role in the formation and maintenance of [[hemidesmosomes]], which are structures that anchor epithelial cells to the [[basement membrane]]. This integrin is involved in [[signal transduction]] pathways that regulate cell survival, proliferation, and migration. It is particularly important in the [[skin]], where it helps maintain the integrity of the [[epidermis]]. | ||
== Clinical significance == | == Clinical significance == | ||
Mutations in the ITGB4 gene | Mutations in the ITGB4 gene can lead to [[epidermolysis bullosa]], a group of genetic conditions that result in fragile skin that blisters easily. The [[α6β4 integrin]] is also implicated in the progression of certain [[cancers]], as it can influence [[tumor cell]] behavior and [[metastasis]]. | ||
== Interactions == | |||
Integrin beta-4 interacts with several proteins, including: | |||
* [[Plectin]], a cytoskeletal linker protein that connects integrins to the intermediate filament network. | |||
* [[Erbin]], a protein that associates with the cytoplasmic domain of integrin beta-4 and is involved in [[cell signaling]]. | |||
== See also == | == See also == | ||
* [[Integrin]] | * [[Integrin]] | ||
* [[Cell adhesion]] | |||
* [[Epidermolysis bullosa]] | * [[Epidermolysis bullosa]] | ||
== References == | == References == | ||
{{Reflist}} | |||
== External links == | == External links == | ||
* | * {{GeneReviews|ITGB4}} | ||
* {{OMIM|147557}} | |||
[[Category:Integrins]] | [[Category:Integrins]] | ||
[[Category:Cell adhesion molecules]] | |||
[[Category:Human proteins]] | |||
[[Category:Genes on human chromosome 17]] | [[Category:Genes on human chromosome 17]] | ||
Latest revision as of 04:30, 29 December 2024
Integrin beta-4 (ITGB4) is a protein that in humans is encoded by the ITGB4 gene. Integrins are transmembrane receptors that facilitate cell-extracellular matrix (ECM) adhesion. They are heterodimeric proteins consisting of alpha and beta subunits. The beta-4 subunit is unique in that it pairs with the alpha-6 subunit to form the α6β4 integrin, which is primarily expressed in epithelial cells.
Function[edit]
Integrin beta-4 plays a critical role in the formation and maintenance of hemidesmosomes, which are structures that anchor epithelial cells to the basement membrane. This integrin is involved in signal transduction pathways that regulate cell survival, proliferation, and migration. It is particularly important in the skin, where it helps maintain the integrity of the epidermis.
Clinical significance[edit]
Mutations in the ITGB4 gene can lead to epidermolysis bullosa, a group of genetic conditions that result in fragile skin that blisters easily. The α6β4 integrin is also implicated in the progression of certain cancers, as it can influence tumor cell behavior and metastasis.
Interactions[edit]
Integrin beta-4 interacts with several proteins, including:
- Plectin, a cytoskeletal linker protein that connects integrins to the intermediate filament network.
- Erbin, a protein that associates with the cytoplasmic domain of integrin beta-4 and is involved in cell signaling.
See also[edit]
References[edit]
<references group="" responsive="1"></references>