ADAM17

ADAM metallopeptidase domain 17 (ADAM17), also called TACE, is a 70-kDa enzyme that belongs to the ADAM protein family of disintegrins and metalloproteases.

Additional recommended knowledge

Better weighing performance in 6 easy steps

Recognize and detect the effects of electrostatic charges on your balance

What is the Correct Way to Check Repeatability in Balances?

Physical Characteristics

ADAM17 is a 824 amino acid polypeptide.^[1]

Enzymes in this family are transmembrane glycoproteins that are characterized by their conserved, multi-domain structure.

Functions

ADAM17 is understood to be involved in the processing of tumor necrosis factor alpha (TNF-α) at the surface of the cell, and from within the intracellular membranes of the trans-Golgi network. This process, which is also known as 'shedding', involves the cleavage and release of a soluble ectodomain from membrane bound pro-proteins (such as pro-TNF-α), and is of known physiological importance. ADAM17 was the first 'sheddase' to be identified, and is also understood to play a role in the release of a diverse variety of membrane-anchored cytokines, cell adhesion molecules, receptors, ligands and enzymes.

Interactions between ADAM17 and pro-TNF-α

Cloning of the TNF-α gene revealed it to encode a 26kDa type II transmembrane pro-polypeptide that becomes inserted into the cell membrane during its maturation. At the cell surface, pro-TNF-α is biologically active, and is able to induce immune responses via juxtacrine intercellular signaling. However, pro-TNF-α can undergo a proteolytic cleavage at its Ala76-Val77 amide bond, which releases a soluble 17kDa extracellular domain (ectodomain) from the pro-TNF-α molecule. This soluble ectodomain is the cytokine commonly known as TNF-α, which is of pivotal importance in paracrine signaling. This proteolytic liberation of soluble TNF-α is catalyzed by ADAM17.

Interactions between ADAM17 and L-selectin

ADAM17 has a role in the shedding of l-selectin, a cellular adhesion molecule.^{[citation needed]}

Cellular Localization of ADAM17

The localization of ADAM17 is speculated to be an important determinant of shedding activity. TNF-α processing has classically been understood to occur in the trans-Golgi network, and be closely-connected to transport of soluble TNF-α to the cell surface. However, research exists that suggests that the majority of mature, endogenous ADAM17 may be localized to a perinuclear compartment, with only a small amount of TACE being present on the cell surface. The localization of mature ADAM17 to a perinulcear compartment therefore raises the possibility that ADAM17-mediated ectodomain shedding may also occur in the intracellular environment, in contrast with the conventional model.

ADAM17 as a target for future medicines?

Since TNF-α is a potent and pivotal mediator in the inflammatory process, considerable investment has been made in the research into- and development of anti-TNF-α agents, for the purpose of reducing the severity of inflammatory responses in disease states (e.g. the medicine Etanercept for treatment of rheumatoid arthritis). The inhibition of ADAM17 by a pharmacological agent may represent another means by which the effects of TNF-α can be modulated, although this is yet to be demonstrated clinically in humans.

Functional ADAM17 has been documented to be ubiquitously expressed in the human colon, with increased activity in the colonic mucosa of patients with ulcerative colitis, a main form of inflammatory bowel disease. These data will no doubt contribute to growing interest in the inhibition of ADAM17 as a potential therapeutic strategy.

Other points of interest

Recent in vitro experiments have provided evidence that suggests that ADAM17 may play a prominent role in the Notch signaling pathway, during the proteolytic release of the Notch intracellular domain (from the Notch1 receptor) that occurs following ligand binding. Other experiments have also suggested that expression of ADAM17 may be inhibited by ethanol.^[2]

References

1. ^ Black R, Rauch C, Kozlosky C, Peschon J, Slack J, Wolfson M, Castner B, Stocking K, Reddy P, Srinivasan S, Nelson N, Boiani N, Schooley K, Gerhart M, Davis R, Fitzner J, Johnson R, Paxton R, March C, Cerretti D (1997). "A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells". Nature 385 (6618): 729-33. PMID 9034190.
2. ^ http://www.jleukbio.org/cgi/reprint/72/6/1142.pdf

Further reading