Biology:ADAM17

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A disintegrin and metalloprotease 17 (ADAM17), also called TACE (tumor necrosis factor-α-converting enzyme), is a 70-kDa enzyme that belongs to the ADAM protein family of disintegrins and metalloproteases, activated by substrate presentation.

Structure

ADAM17 is an 824-amino acid polypeptide.[1][2]

ADAM17 has multidomain structure that includes a pro-domain, a metallo-protease domain, a disintegrin domain, a cysteine-rich domain, an EGF-like domain, a transmembrane domain, and a cytoplasmic tail.[3][4][5] The metalloprotease domain is responsible for the enzyme's catalytic activity, cleaving membrane-bound proteins, including cytokines like TNF-alpha, to release their soluble forms. The disintegrin and cysteine-rich domains are implicated in cell adhesion and interaction with integrins, while the transmembrane domain anchors the protein in the membrane. The cytoplasmic tail is involved in intracellular signaling and protein-protein interactions. ADAM17's activity is tightly regulated through multiple mechanisms, including the removal of its pro-domain and interactions with regulatory proteins such as TIMPs (tissue inhibitors of metalloproteinases).[6]

Function

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.

Cloning of the TNF-α gene revealed it to encode a 26 kDa 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.

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. ADAM17 also regulates the MAP kinase signaling pathway by regulating shedding of the EGFR ligand amphiregulin in the mammary gland.[7] ADAM17 also has a role in the shedding of L-selectin, a cellular adhesion molecule.[8]

Activation

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. Shedding is also associated with clustering of ADAM17 with its substrate, membrane bound TNF, in lipid rafts. [9] The overall process is called substrate presentation and regulated by cholesterol. Research also 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 perinuclear compartment, therefore, raises the possibility that ADAM17-mediated ectodomain shedding may also occur in the intracellular environment, in contrast with the conventional model.

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. Other experiments have also suggested that expression of ADAM17 may be inhibited by ethanol.[10]

Interactions

ADAM17 has been shown to interact with:

Clinical significance

Adam17 may facilitate entry of the SARS‑CoV‑2 virus, possibly by enabling fusion of virus particles with the cytoplasmic membrane.[16] Adam17 has similar ACE2 cleavage activity as TMPRSS2, but by forming soluble ACE2, Adam17 may actually have the protective effect of blocking circulating SARS‑CoV‑2 virus particles.[16]

Adam17 sheddase activity may contribute to COVID-19 inflammation by cleavage of TNF-α and Interleukin-6 receptor.[16]

Recently, ADAM17 was discovered as a crucial mediator of resistance to radiotherapy. Radiotherapy can induce a dose-dependent increase of furin-mediated cleavage of the ADAM17 proform to active ADAM17, which results in enhanced ADAM17 activity in vitro and in vivo. It was also shown that radiotherapy activates ADAM17 in non-small cell lung cancer, which results in shedding of multiple survival factors, growth factor pathway activation, and radiotherapy-induced treatment resistance.[17]

References

  1. ↑ "A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells". Nature 385 (6618): 729–733. February 1997. doi:10.1038/385729a0. PMID 9034190. Bibcode: 1997Natur.385..729B. 
  2. ↑ "Cloning of a disintegrin metalloproteinase that processes precursor tumour-necrosis factor-alpha". Nature 385 (6618): 733–736. February 1997. doi:10.1038/385733a0. PMID 9034191. Bibcode: 1997Natur.385..733M. 
  3. ↑ "The ADAM gene family: surface proteins with adhesion and protease activity". Trends in Genetics 16 (2): 83–87. February 2000. doi:10.1016/s0168-9525(99)01926-5. PMID 10652535. 
  4. ↑ "The ADAMs family of metalloproteases: multidomain proteins with multiple functions". Genes & Development 17 (1): 7–30. January 2003. doi:10.1101/gad.1039703. PMID 12514095. 
  5. ↑ "ADAMs: key components in EGFR signalling and development". Nature Reviews. Molecular Cell Biology 6 (1): 32–43. January 2005. doi:10.1038/nrm1548. PMID 15688065. 
  6. ↑ "The ADAM metalloproteinases". Molecular Aspects of Medicine 29 (5): 258–289. October 2008. doi:10.1016/j.mam.2008.08.001. PMID 18762209. 
  7. ↑ "Mammary ductal morphogenesis requires paracrine activation of stromal EGFR via ADAM17-dependent shedding of epithelial amphiregulin". Development 132 (17): 3923–3933. September 2005. doi:10.1242/dev.01966. PMID 16079154. 
  8. ↑ "ADAM17 deficiency by mature neutrophils has differential effects on L-selectin shedding". Blood 108 (7): 2275–2279. October 2006. doi:10.1182/blood-2006-02-005827. PMID 16735599. 
  9. ↑ "The shedding activity of ADAM17 is sequestered in lipid rafts". Experimental Cell Research 312 (20): 3969–3980. December 2006. doi:10.1016/j.yexcr.2006.08.027. PMID 17010968. 
  10. ↑ "Ethanol-induced inhibition of cytokine release and protein degranulation in human neutrophils". Journal of Leukocyte Biology 72 (6): 1142–1147. December 2002. doi:10.1189/jlb.72.6.1142. PMID 12488495. 
  11. ↑ "Identification of SAP97 as an intracellular binding partner of TACE". Journal of Cell Science 116 (Pt 10): 1949–1957. May 2003. doi:10.1242/jcs.00415. PMID 12668732. 
  12. ↑ "Evidence for an interaction of the metalloprotease-disintegrin tumour necrosis factor alpha convertase (TACE) with mitotic arrest deficient 2 (MAD2), and of the metalloprotease-disintegrin MDC9 with a novel MAD2-related protein, MAD2beta". The Biochemical Journal 343 Pt 3 (Pt 3): 673–680. November 1999. doi:10.1042/0264-6021:3430673. PMID 10527948. 
  13. ↑ "Phosphorylation-dependent interactions between ADAM15 cytoplasmic domain and Src family protein-tyrosine kinases". The Journal of Biological Chemistry 277 (7): 4999–5007. February 2002. doi:10.1074/jbc.M107430200. PMID 11741929. 
  14. ↑ "Extracellular signal-regulated kinase phosphorylates tumor necrosis factor alpha-converting enzyme at threonine 735: a potential role in regulated shedding". Molecular Biology of the Cell 13 (6): 2031–2044. June 2002. doi:10.1091/mbc.01-11-0561. PMID 12058067. 
  15. ↑ "Phosphorylation of iRhom2 at the plasma membrane controls mammalian TACE-dependent inflammatory and growth factor signalling". eLife 6. April 2017. doi:10.7554/eLife.23968. PMID 28432785. 
  16. ↑ 16.0 16.1 16.2 "ACE2/ADAM17/TMPRSS2 Interplay May Be the Main Risk Factor for COVID-19". Frontiers in Immunology 11. 2020. doi:10.3389/fimmu.2020.576745. PMID 33117379. 
  17. ↑ "Secretome Signature Identifies ADAM17 as Novel Target for Radiosensitization of Non-Small Cell Lung Cancer". Clinical Cancer Research 22 (17): 4428–4439. September 2016. doi:10.1158/1078-0432.CCR-15-2449. PMID 27076628. 

Further reading



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