View source for Biology:ADAM17

{{Short description|Protein-coding gene in the species Homo sapiens}}
{{Infobox_gene}}
A disintegrin and metalloprotease 17 ('''ADAM17'''), also called '''TACE''' (''tumor necrosis factor-α-converting enzyme''), is a 70-kDa [[Biology:Enzyme|enzyme]] that belongs to the ADAM protein family of disintegrins and metalloproteases.

== Chemical characteristics ==

ADAM17 is an 824-[[Chemistry:Amino acid|amino acid]] polypeptide.<ref name="pmid9034190">{{cite journal | vauthors = Black RA, Rauch CT, Kozlosky CJ, Peschon JJ, Slack JL, Wolfson MF, Castner BJ, Stocking KL, Reddy P, Srinivasan S, Nelson N, Boiani N, Schooley KA, Gerhart M, Davis R, Fitzner JN, Johnson RS, Paxton RJ, March CJ, Cerretti DP | title = A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells | journal = Nature | volume = 385 | issue = 6618 | pages = 729–33 | date = February 1997 | pmid = 9034190 | doi = 10.1038/385729a0 | bibcode = 1997Natur.385..729B | s2cid = 4251053 }}</ref><ref name="pmid9034191">{{cite journal | vauthors = Moss ML, Jin SL, Milla ME, Bickett DM, Burkhart W, Carter HL, Chen WJ, Clay WC, Didsbury JR, Hassler D, Hoffman CR, Kost TA, Lambert MH, Leesnitzer MA, McCauley P, McGeehan G, Mitchell J, Moyer M, Pahel G, Rocque W, Overton LK, Schoenen F, Seaton T, Su JL, Becherer JD | title = Cloning of a disintegrin metalloproteinase that processes precursor tumour-necrosis factor-alpha | journal = Nature | volume = 385 | issue = 6618 | pages = 733–6 | date = February 1997 | pmid = 9034191 | doi = 10.1038/385733a0 | bibcode = 1997Natur.385..733M | s2cid = 4335616 }}</ref>

== Function ==

ADAM17 is understood to be involved in the processing of tumor necrosis factor alpha (TNF-α) at the surface of the [[Biology:Cell|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 '[[Biology:Sheddase|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, [[Biology:Receptor (biochemistry)|receptors]], ligands, and enzymes.

Cloning of the TNF-α [[Biology:Gene|gene]] revealed it to encode a 26&nbsp;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 [[Biology:Protease|proteolytic cleavage]] at its Ala76-Val77 amide bond, which releases a soluble 17kDa extracellular domain ([[Biology:Ectodomain|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.

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.<ref name="pmid27076628">{{cite journal | vauthors = Sharma A, Bender S, Zimmermann M, Riesterer O, Broggini-Tenzer A, Pruschy MN | title = Secretome Signature Identifies ADAM17 as Novel Target for Radiosensitization of Non-Small Cell Lung Cancer | journal = Clinical Cancer Research | volume = 22 | issue = 17 | pages = 4428–39 | date = September 2016 | pmid = 27076628 | doi = 10.1158/1078-0432.CCR-15-2449 | doi-access = free }}</ref>

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.<ref name="pmid16079154">{{cite journal | vauthors = Sternlicht MD, Sunnarborg SW, Kouros-Mehr H, Yu Y, Lee DC, Werb Z | title = Mammary ductal morphogenesis requires paracrine activation of stromal EGFR via ADAM17-dependent shedding of epithelial amphiregulin | journal = Development | volume = 132 | issue = 17 | pages = 3923–33 | date = September 2005 | pmid = 16079154 | pmc = 2771180 | doi = 10.1242/dev.01966 }}</ref> ADAM17 also has a role in the shedding of L-selectin, a [[Biology:Cell adhesion molecule|cellular adhesion molecule]].<ref name="pmid16735599">{{cite journal | vauthors = Li Y, Brazzell J, Herrera A, Walcheck B | title = ADAM17 deficiency by mature neutrophils has differential effects on L-selectin shedding | journal = Blood | volume = 108 | issue = 7 | pages = 2275–9 | date = October 2006 | pmid = 16735599 | pmc = 1895557 | doi = 10.1182/blood-2006-02-005827 }}</ref>

== Interactions ==

ADAM17 has been shown to interact with:
* [[Biology:DLG1|DLG1]]<ref name = pmid12668732>{{cite journal | vauthors = Peiretti F, Deprez-Beauclair P, Bonardo B, Aubert H, Juhan-Vague I, Nalbone G | title = Identification of SAP97 as an intracellular binding partner of TACE | journal = Journal of Cell Science | volume = 116 | issue = Pt 10 | pages = 1949–57 | date = May 2003 | pmid = 12668732 | doi = 10.1242/jcs.00415 | doi-access = free }}</ref> 
* MAD2L1,<ref name = pmid10527948>{{cite journal | vauthors = Nelson KK, Schlöndorff J, Blobel CP | title = 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 | journal = The Biochemical Journal | volume = 343 Pt 3 | issue = 3 | pages = 673–80 | date = November 1999 | pmid = 10527948 | pmc = 1220601 | doi = 10.1042/0264-6021:3430673 }}</ref><ref name = pmid11741929>{{cite journal | vauthors = Poghosyan Z, Robbins SM, Houslay MD, Webster A, Murphy G, Edwards DR | title = Phosphorylation-dependent interactions between ADAM15 cytoplasmic domain and Src family protein-tyrosine kinases | journal = The Journal of Biological Chemistry | volume = 277 | issue = 7 | pages = 4999–5007 | date = February 2002 | pmid = 11741929 | doi = 10.1074/jbc.M107430200 | doi-access = free }}</ref> and
* [[Biology:MAPK1|MAPK1]].<ref name = pmid12058067>{{cite journal | vauthors = Díaz-Rodríguez E, Montero JC, Esparís-Ogando A, Yuste L, Pandiella A | title = Extracellular signal-regulated kinase phosphorylates tumor necrosis factor alpha-converting enzyme at threonine 735: a potential role in regulated shedding | journal = Molecular Biology of the Cell | volume = 13 | issue = 6 | pages = 2031–44 | date = June 2002 | pmid = 12058067 | pmc = 117622 | doi = 10.1091/mbc.01-11-0561 }}</ref>

== 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. <ref>{{cite journal |last1=Tellier |first1=Edwige |last2=Canault |first2=Matthias |last3=Rebsomen |first3=Laure |last4=Bonardo |first4=Bernadette |last5=Juhan-Vague |first5=Irène |last6=Nalbone |first6=Gilles |last7=Peiretti |first7=Franck |title=The shedding activity of ADAM17 is sequestered in lipid rafts |journal=Experimental Cell Research |date=10 December 2006 |volume=312 |issue=20 |pages=3969–3980 |doi=10.1016/j.yexcr.2006.08.027 |pmid=17010968 }}</ref> The overall process is called [[Biology:Substrate presentation|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 [[Medicine:Ulcerative colitis|ulcerative colitis]], a main form of [[Medicine:Inflammatory bowel disease|inflammatory bowel disease]]. Other experiments have also suggested that expression of ADAM17 may be inhibited by [[Chemistry:Ethanol|ethanol]].<ref name="pmid12488495">{{cite journal | vauthors = Taïeb J, Delarche C, Ethuin F, Selloum S, Poynard T, Gougerot-Pocidalo MA, Chollet-Martin S | title = Ethanol-induced inhibition of cytokine release and protein degranulation in human neutrophils | journal = Journal of Leukocyte Biology | volume = 72 | issue = 6 | pages = 1142–7 | date = December 2002 | doi = 10.1189/jlb.72.6.1142 | pmid = 12488495 | s2cid = 9712196 }}</ref>

== Clinical significance ==
Adam17 may facilitate entry of the [[Biology:Severe acute respiratory syndrome coronavirus 2|SARS‑CoV‑2]] virus, possibly by enabling fusion of virus particles with the cytoplasmic membrane.<ref name="pmid33117379">{{cite journal | vauthors = Zipeto D, Argañaraz GA, Argañaraz ER | title = ACE2/ADAM17/TMPRSS2 Interplay May Be the Main Risk Factor for COVID-19 | journal = Frontiers in Immunology | volume = 11  | pages = 576745 | date = 2020 | doi = 10.3389/fimmu.2020.576745 | pmc = 7575774 | pmid = 33117379| doi-access = free }}</ref> Adam17 has similar [[Biology:Angiotensin-converting enzyme 2|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.<ref name="pmid33117379" /> 

Adam17 sheddase activity may contribute to COVID-19 inflammation by cleavage of [[Biology:Tumor necrosis factor|TNF-α]] and [[Biology:Interleukin-6 receptor|Interleukin-6 receptor]].<ref name="pmid33117379" />

== References ==
{{Reflist|35em}}

== Further reading ==
{{ref begin|35em}}
* {{cite journal | vauthors = Black RA | title = Tumor necrosis factor-alpha converting enzyme | journal = The International Journal of Biochemistry & Cell Biology | volume = 34 | issue = 1 | pages = 1–5 | date = January 2002 | pmid = 11733179 | doi = 10.1016/S1357-2725(01)00097-8 }}
* {{cite journal | vauthors = Bonaldo MF, Lennon G, Soares MB | title = Normalization and subtraction: two approaches to facilitate gene discovery | journal = Genome Research | volume = 6 | issue = 9 | pages = 791–806 | date = September 1996 | pmid = 8889548 | doi = 10.1101/gr.6.9.791 | doi-access = free }}
* {{cite journal | vauthors = Black RA, Rauch CT, Kozlosky CJ, Peschon JJ, Slack JL, Wolfson MF, Castner BJ, Stocking KL, Reddy P, Srinivasan S, Nelson N, Boiani N, Schooley KA, Gerhart M, Davis R, Fitzner JN, Johnson RS, Paxton RJ, March CJ, Cerretti DP | title = A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells | journal = Nature | volume = 385 | issue = 6618 | pages = 729–33 | date = February 1997 | pmid = 9034190 | doi = 10.1038/385729a0 | bibcode = 1997Natur.385..729B | s2cid = 4251053 }}
* {{cite journal | vauthors = Moss ML, Jin SL, Milla ME, Bickett DM, Burkhart W, Carter HL, Chen WJ, Clay WC, Didsbury JR, Hassler D, Hoffman CR, Kost TA, Lambert MH, Leesnitzer MA, McCauley P, McGeehan G, Mitchell J, Moyer M, Pahel G, Rocque W, Overton LK, Schoenen F, Seaton T, Su JL, Becherer JD | title = Cloning of a disintegrin metalloproteinase that processes precursor tumour-necrosis factor-alpha | journal = Nature | volume = 385 | issue = 6618 | pages = 733–6 | date = February 1997 | pmid = 9034191 | doi = 10.1038/385733a0 | bibcode = 1997Natur.385..733M | s2cid = 4335616 }}
* {{cite journal | vauthors = Maskos K, Fernandez-Catalan C, Huber R, Bourenkov GP, Bartunik H, Ellestad GA, Reddy P, Wolfson MF, Rauch CT, Castner BJ, Davis R, Clarke HR, Petersen M, Fitzner JN, Cerretti DP, March CJ, Paxton RJ, Black RA, Bode W | title = Crystal structure of the catalytic domain of human tumor necrosis factor-alpha-converting enzyme | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 95 | issue = 7 | pages = 3408–12 | date = March 1998 | pmid = 9520379 | pmc = 19849 | doi = 10.1073/pnas.95.7.3408 | bibcode = 1998PNAS...95.3408M | doi-access = free }}
* {{cite journal | vauthors = Patel IR, Attur MG, Patel RN, Stuchin SA, Abagyan RA, Abramson SB, Amin AR | title = TNF-alpha convertase enzyme from human arthritis-affected cartilage: isolation of cDNA by differential display, expression of the active enzyme, and regulation of TNF-alpha | journal = Journal of Immunology | volume = 160 | issue = 9 | pages = 4570–9 | date = May 1998 | doi = 10.4049/jimmunol.160.9.4570 | pmid = 9574564 | s2cid = 54023449 | doi-access = free }}
* {{cite journal | vauthors = Schroeter EH, Kisslinger JA, Kopan R | title = Notch-1 signalling requires ligand-induced proteolytic release of intracellular domain | journal = Nature | volume = 393 | issue = 6683 | pages = 382–6 | date = May 1998 | pmid = 9620803 | doi = 10.1038/30756 | bibcode = 1998Natur.393..382S | s2cid = 4431882 }}
* {{cite journal | vauthors = Hirohata S, Seldin MF, Apte SS | title = Chromosomal assignment of two ADAM genes, TACE (ADAM17) and MLTNB (ADAM19), to human chromosomes 2 and 5, respectively, and of Mltnb to mouse chromosome 11 | journal = Genomics | volume = 54 | issue = 1 | pages = 178–9 | date = November 1998 | pmid = 9806848 | doi = 10.1006/geno.1998.5544 }}
* {{cite journal | vauthors = Lum L, Wong BR, Josien R, Becherer JD, Erdjument-Bromage H, Schlöndorff J, Tempst P, Choi Y, Blobel CP | title = Evidence for a role of a tumor necrosis factor-alpha (TNF-alpha)-converting enzyme-like protease in shedding of TRANCE, a TNF family member involved in osteoclastogenesis and dendritic cell survival | journal = The Journal of Biological Chemistry | volume = 274 | issue = 19 | pages = 13613–8 | date = May 1999 | pmid = 10224132 | doi = 10.1074/jbc.274.19.13613 | doi-access = free }}
* {{cite journal | vauthors = Cerretti DP, Poindexter K, Castner BJ, Means G, Copeland NG, Gilbert DJ, Jenkins NA, Black RA, Nelson N | title = Characterization of the cDNA and gene for mouse tumour necrosis factor alpha converting enzyme (TACE/ADAM17) and its location to mouse chromosome 12 and human chromosome 2p25 | journal = Cytokine | volume = 11 | issue = 8 | pages = 541–51 | date = August 1999 | pmid = 10433800 | doi = 10.1006/cyto.1998.0466 }}
* {{cite journal | vauthors = Nelson KK, Schlöndorff J, Blobel CP | title = 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 | journal = The Biochemical Journal | volume = 343 Pt 3 | issue = Pt 3 | pages = 673–80 | date = November 1999 | pmid = 10527948 | pmc = 1220601 | doi = 10.1042/0264-6021:3430673 }}
* {{cite journal | vauthors = Kärkkäinen I, Rybnikova E, Pelto-Huikko M, Huovila AP | title = Metalloprotease-disintegrin (ADAM) genes are widely and differentially expressed in the adult CNS | journal = Molecular and Cellular Neurosciences | volume = 15 | issue = 6 | pages = 547–60 | date = June 2000 | pmid = 10860581 | doi = 10.1006/mcne.2000.0848 | s2cid = 36643322 }}
* {{cite journal | vauthors = Brou C, Logeat F, Gupta N, Bessia C, LeBail O, Doedens JR, Cumano A, Roux P, Black RA, Israël A | title = A novel proteolytic cleavage involved in Notch signaling: the role of the disintegrin-metalloprotease TACE | journal = Molecular Cell | volume = 5 | issue = 2 | pages = 207–16 | date = February 2000 | pmid = 10882063 | doi = 10.1016/S1097-2765(00)80417-7 | doi-access = free }}
* {{cite journal | vauthors = Lee MH, Verma V, Maskos K, Nath D, Knäuper V, Dodds P, Amour A, Murphy G | title = Engineering N-terminal domain of tissue inhibitor of metalloproteinase (TIMP)-3 to be a better inhibitor against tumour necrosis factor-alpha-converting enzyme | journal = The Biochemical Journal | volume = 364 | issue = Pt 1 | pages = 227–34 | date = May 2002 | pmid = 11988096 | pmc = 1222565 | doi =  10.1042/bj3640227}}
* {{cite journal | vauthors = Lee MH, Verma V, Maskos K, Becherer JD, Knäuper V, Dodds P, Amour A, Murphy G | title = The C-terminal domains of TACE weaken the inhibitory action of N-TIMP-3 | journal = FEBS Letters | volume = 520 | issue = 1–3 | pages = 102–6 | date = June 2002 | pmid = 12044879 | doi = 10.1016/S0014-5793(02)02776-X | s2cid = 1433047 }}
* {{cite journal | vauthors = Díaz-Rodríguez E, Montero JC, Esparís-Ogando A, Yuste L, Pandiella A | title = Extracellular signal-regulated kinase phosphorylates tumor necrosis factor alpha-converting enzyme at threonine 735: a potential role in regulated shedding | journal = Molecular Biology of the Cell | volume = 13 | issue = 6 | pages = 2031–44 | date = June 2002 | pmid = 12058067 | pmc = 117622 | doi = 10.1091/mbc.01-11-0561 }}
* {{cite journal | vauthors = Mohan MJ, Seaton T, Mitchell J, Howe A, Blackburn K, Burkhart W, Moyer M, Patel I, Waitt GM, Becherer JD, Moss ML, Milla ME | title = The tumor necrosis factor-alpha converting enzyme (TACE): a unique metalloproteinase with highly defined substrate selectivity | journal = Biochemistry | volume = 41 | issue = 30 | pages = 9462–9 | date = July 2002 | pmid = 12135369 | doi = 10.1021/bi0260132 }}
* {{cite journal | vauthors = Gómez-Gaviro MV, González-Alvaro I, Domínguez-Jiménez C, Peschon J, Black RA, Sánchez-Madrid F, Díaz-González F | title = Structure-function relationship and role of tumor necrosis factor-alpha-converting enzyme in the down-regulation of L-selectin by non-steroidal anti-inflammatory drugs | journal = The Journal of Biological Chemistry | volume = 277 | issue = 41 | pages = 38212–21 | date = October 2002 | pmid = 12147693 | doi = 10.1074/jbc.M205142200 | doi-access = free }}
* {{cite journal | vauthors = Zheng Y, Schlondorff J, Blobel CP | title = Evidence for regulation of the tumor necrosis factor alpha-convertase (TACE) by protein-tyrosine phosphatase PTPH1 | journal = The Journal of Biological Chemistry | volume = 277 | issue = 45 | pages = 42463–70 | date = November 2002 | pmid = 12207026 | doi = 10.1074/jbc.M207459200 | doi-access = free }}
{{refend}}

== External links ==
* {{MeshName|CD156b+Antigen}}
* {{UCSC gene info|ADAM17}}
* {{UCSC gene info|ADAM18}}

{{PDB Gallery|geneid=6868}}
{{Clusters of differentiation}}
{{Metalloendopeptidases}}
{{Enzymes}}

{{DEFAULTSORT:Adam17}}
[[Category:Clusters of differentiation]]
[[Category:EC 3.4.24]]
[[Category:Signal transduction]]
[[Category:Human proteins]]

{{Sourceattribution|ADAM17}}