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{{Short description|Mammalian protein found in Homo sapiens}}
{{PBB|geneid=57007}}
{{Infobox_gene}}
'''C-X-C chemokine receptor type 7''' (CXCR-7) is a [[protein]] that in humans is encoded by the ''CXCR7'' [[gene]].<ref name="pmid16107333">{{cite journal | author = Balabanian K, Lagane B, Infantino S, Chow KY, Harriague J, Moepps B, Arenzana-Seisdedos F, Thelen M, Bachelerie F | title = The chemokine SDF-1/CXCL12 binds to and signals through the orphan receptor RDC1 in T lymphocytes | journal = J Biol Chem | volume = 280 | issue = 42 | pages = 35760–6 |date=Oct 2005 | pmid = 16107333 | pmc = | doi = 10.1074/jbc.M508234200 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: CXCR7 chemokine (C-X-C motif) receptor 7| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=57007| accessdate = }}</ref>
'''Atypical chemokine receptor 3''' also known as '''C-X-C chemokine receptor type 7''' (CXCR-7) and '''G-protein coupled receptor 159''' (GPR159) is a [[protein]] that in humans is encoded by the ''ACKR3'' [[gene]].<ref name="pmid16107333">{{cite journal | vauthors = Balabanian K, Lagane B, Infantino S, Chow KY, Harriague J, Moepps B, Arenzana-Seisdedos F, Thelen M, Bachelerie F | display-authors = 6 | title = The chemokine SDF-1/CXCL12 binds to and signals through the orphan receptor RDC1 in T lymphocytes | journal = The Journal of Biological Chemistry | volume = 280 | issue = 42 | pages = 35760–35766 | date = October 2005 | pmid = 16107333 | doi = 10.1074/jbc.M508234200 | doi-access = free }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: CXCR7 chemokine (C-X-C motif) receptor 7| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=57007}}</ref>


This gene encodes a member of the [[G protein-coupled receptor]] family. This protein was earlier thought to be a receptor for vasoactive intestinal peptide (VIP) and was considered to be an orphan receptor. It is now classified as a [[chemokine receptor]] able to bind the chemokines [[CXCL12]]/SDF-1 and [[CXCL11]]. The protein is also a coreceptor for human immunodeficiency viruses (HIV). Translocations involving this gene and HMGA2 on chromosome 12 have been observed in lipomas. Alternatively spliced transcript variants encoding the same protein isoform have been found for this gene. Whereas some reports claim that the receptor induces signaling following ligand binding, recent findings in zebrafish suggest that CXCR7 functions primarily by sequestering the chemokine CXCL12.<ref name="entrez"/>
This gene encodes a [[G protein-coupled receptor]] family member. It belongs to the [[chemokine receptor]] family of GPCRs. Within this family, ACKR3 is classified as a class A GPCR.<ref>{{cite journal | vauthors = Fumagalli A, Zarca A, Neves M, Caspar B, Hill SJ, Mayor F, Smit MJ, Marin P | display-authors = 6 | title = CXCR4/ACKR3 Phosphorylation and Recruitment of Interacting Proteins: Key Mechanisms Regulating Their Functional Status | journal = Molecular Pharmacology | volume = 96 | issue = 6 | pages = 794–808 | date = December 2019 | pmid = 30837297 | doi = 10.1124/mol.118.115360 | s2cid = 73513931 | doi-access = free | hdl = 10261/214032 | hdl-access = free }}</ref> This GPCR protein was earlier thought to be a receptor for vasoactive intestinal peptide (VIP) and was considered to be an orphan receptor. It is now classified as a [[chemokine receptor]] able to bind the chemokines [[CXCL12]]/SDF-1 and [[CXCL11]]. The protein is also a coreceptor for [[human immunodeficiency virus]]es (HIV). Translocations involving this gene and HMGA2 on chromosome 12 have been observed in lipomas. Alternatively spliced transcript variants encoding the same protein isoform have been found for this gene. Whereas some reports claim that the receptor induces signaling following ligand binding, recent findings in zebrafish suggest that CXCR7 functions primarily by sequestering the chemokine CXCL12.<ref name="entrez"/>


However, another recent study has provided evidence that ligand binding to CXCR7 activates MAP kinases through Beta-arrestins, and thus has functions beyond ligand sequestration.<ref name="pmid20018651">*{{cite journal | doi=10.1073/pnas.0912852107 | author=Rajagopal, Sudarshan. ''et al.'' |title=B-arrestin-but not G protein-mediated signaling by the "decoy" receptor CXCR7. |journal=PNAS |volume=107 |issue=2 |pages= 628–632 |year= 2009 |pmid=20018651 | pmc=2818968}}</ref>
Another study has provided evidence that ligand binding to CXCR7 activates MAP kinases through Beta-arrestins, and thus has functions beyond ligand sequestration.<ref name="pmid20018651">* {{cite journal | vauthors = Rajagopal S, Kim J, Ahn S, Craig S, Lam CM, Gerard NP, Gerard C, Lefkowitz RJ | display-authors = 6 | title = Beta-arrestin- but not G protein-mediated signaling by the "decoy" receptor CXCR7 | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 107 | issue = 2 | pages = 628–632 | date = January 2010 | pmid = 20018651 | pmc = 2818968 | doi = 10.1073/pnas.0912852107 | doi-access = free | bibcode = 2010PNAS..107..628R }}</ref>


ACKR3 has also been shown to sequester [[endogenous]] [[opioid peptide]]s and is thought to modulate their activity.<ref name="Meyrath_2-2-" />
⚫
==References==

== Nomenclature ==
In 2013, the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology subcommittee for chemokine receptors reevaluated C-X-C chemokine receptor type 7 (CXCR7) and classified it as an atypical chemokine receptor, leading to its renaming as atypical chemokine receptor 3 (ACKR3). Additional names that have been mentioned in the literature, albeit less frequently, include GPR159 and Orphan receptor RDC1, the latter being a term primarily found in older literature.<ref>{{cite journal | vauthors = Bachelerie F, Graham GJ, Locati M, Mantovani A, Murphy PM, Nibbs R, Rot A, Sozzani S, Thelen M | display-authors = 6 | title = New nomenclature for atypical chemokine receptors | journal = Nature Immunology | volume = 15 | issue = 3 | pages = 207–208 | date = March 2014 | pmid = 24549061 | doi = 10.1038/ni.2812 | s2cid = 205367583 }}</ref>

== Function ==
ACKR3 stands out as an atypical receptor due to its β-arrestin-biased signaling nature. In the case of a β-arrestin-biased receptor like ACKR3, when it is treated with an unbiased ligand, it triggers signaling pathways solely mediated by β-arrestin. What sets ACKR3 apart is its absence of G-protein involvement, which distinguishes it from typical GPCRs.<ref>{{cite journal | vauthors = Rajagopal S, Kim J, Ahn S, Craig S, Lam CM, Gerard NP, Gerard C, Lefkowitz RJ | display-authors = 6 | title = Beta-arrestin- but not G protein-mediated signaling by the "decoy" receptor CXCR7 | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 107 | issue = 2 | pages = 628–632 | date = January 2010 | pmid = 20018651 | pmc = 2818968 | doi = 10.1073/pnas.0912852107 | bibcode = 2010PNAS..107..628R | doi-access = free }}</ref>

Despite being considered atypical, the functions of ACKR3 do not imply that it acts as a completely inactive receptor for CXCL12. On the contrary, extensive literature supports the notion of ACKR3 engaging in active signaling, which is believed to rely on arrestin-mediated mechanisms. Nevertheless, its role as a decoy receptor for CXCL12/SDF1 is well-established. This is evident by the significantly higher affinity of CXCL12 binding to ACKR3/CXCR7 compared to CXCR4, along with its constant internalization facilitated by the recruitment of β-arrestin, without known downstream signaling events.<ref name=":0">{{cite journal | vauthors = Koch C, Engele J | title = Functions of the CXCL12 Receptor ACKR3/CXCR7-What Has Been Perceived and What Has Been Overlooked | journal = Molecular Pharmacology | volume = 98 | issue = 5 | pages = 577–585 | date = November 2020 | pmid = 32883765 | doi = 10.1124/molpharm.120.000056 | s2cid = 221498026 | doi-access = free }}</ref><ref>{{cite journal | vauthors = Pance K, Gramespacher JA, Byrnes JR, Salangsang F, Serrano JC, Cotton AD, Steri V, Wells JA | display-authors = 6 | title = Modular cytokine receptor-targeting chimeras for targeted degradation of cell surface and extracellular proteins | journal = Nature Biotechnology | volume = 41 | issue = 2 | pages = 273–281 | date = February 2023 | pmid = 36138170 | doi = 10.1038/s41587-022-01456-2 | pmc = 9931583 }}</ref>

==Ligands==
In addition to CXCL12, ACKR3 engages with multiple ligands, encompassing [[CXCL11]], [[macrophage migration inhibitory factor|macrophage inhibitory factor]] (MIF), [[adrenomedullin]] (ADM), opioid peptides such as [[nociceptin]], [[dynorphin]], and [[enkephalin]], as well as the viral chemokine vCCL2/viral macrophage inflammatory protein-II. <ref name=":0" /><ref>{{cite journal | vauthors = Meyrath M, Szpakowska M, Zeiner J, Massotte L, Merz MP, Benkel T, Simon K, Ohnmacht J, Turner JD, Krüger R, Seutin V, Ollert M, Kostenis E, Chevigné A | display-authors = 6 | title = The atypical chemokine receptor ACKR3/CXCR7 is a broad-spectrum scavenger for opioid peptides | journal = Nature Communications | volume = 11 | issue = 1 | pages = 3033 | date = June 2020 | pmid = 32561830 | doi = 10.1038/s41467-020-16664-0 | pmc = 7305236 | bibcode = 2020NatCo..11.3033M }}</ref>

Inhibition of ACKR3 by [[ligand (biochemistry)|ligand]]s such as the peptide [[LIH383]] (FGGFMRRK-NH<sub>2</sub>) and the [[small molecule]]s [[conolidine]], [[RTI-5152-12]], and [[VUF15485]] increases opioid peptide activity and produces [[analgesic]] and [[antidepressant]] effects in [[animal model|animal studies]].<ref name="Meyrath_2-2-">{{cite journal | vauthors = Meyrath M, Szpakowska M, Zeiner J, Massotte L, Merz MP, Benkel T, Simon K, Ohnmacht J, Turner JD, Krüger R, Seutin V, Ollert M, Kostenis E, Chevigné A | display-authors = 6 | title = The atypical chemokine receptor ACKR3/CXCR7 is a broad-spectrum scavenger for opioid peptides | journal = Nature Communications | volume = 11 | issue = 1 | pages = 3033 | date = June 2020 | pmid = 32561830 | pmc = 7305236 | doi = 10.1038/s41467-020-16664-0 | doi-access = free | bibcode = 2020NatCo..11.3033M }}</ref><ref name="SzpakowskaDeckerMeyrath2021">{{cite journal | vauthors = Szpakowska M, Decker AM, Meyrath M, Palmer CB, Blough BE, Namjoshi OA, Chevigné A | title = The natural analgesic conolidine targets the newly identified opioid scavenger ACKR3/CXCR7 | journal = Signal Transduct Target Ther | volume = 6 | issue = 1 | pages = 209 | date = June 2021 | pmid = 34075018 | pmc = 8169647 | doi = 10.1038/s41392-021-00548-w | url = }}</ref><ref name="ZarcaAdlereViciano2024">{{cite journal | vauthors = Zarca AM, Adlere I, Viciano CP, Arimont-Segura M, Meyrath M, Simon IA, Bebelman JP, Laan D, Custers HG, Janssen E, Versteegh KL, Buzink MC, Nesheva DN, Bosma R, de Esch IJ, Vischer HF, Wijtmans M, Szpakowska M, Chevigné A, Hoffmann C, de Graaf C, Zarzycka BA, Windhorst AD, Smit MJ, Leurs R | title = Pharmacological Characterization and Radiolabeling of VUF15485, a High-Affinity Small-Molecule Agonist for the Atypical Chemokine Receptor ACKR3 | journal = Mol Pharmacol | volume = 105 | issue = 4 | pages = 301–312 | date = March 2024 | pmid = 38346795 | doi = 10.1124/molpharm.123.000835 | url =https://www.biorxiv.org/content/biorxiv/early/2023/07/12/2023.07.12.548622.full.pdf }}</ref>

== Interactions ==
ACKR3 and CXCR4 have been shown to interact, different possibilities regarding the involvement of ACKR3 and CXCR4 in CXCL12 signaling:<ref name=":0" />

A) ACKR3 can attenuate CXCR4 signaling by forming heterodimers with CXCR4. While this interaction was initially observed in cells with CXCR7 overexpression, it has rarely been observed with endogenous CXCR7.

B) Multiple cell types demonstrate that either ACKR3 or CXCR4 controls specific cell functions (e.g., migration, proliferation). The distinct regulation of these functions occurs through one of the receptors.

C) Synergistic effects between CXCR4 and ACKR3 have been observed in many cases, suggesting that cellular responses to CXCL12 require the presence of both receptors. Whether receptor heterodimerization is responsible for these synergistic effects remains uncertain.

D) In addition to synergistic effects, a few studies have shown additive effects of ACKR3 and CXCR4 on specific cell functions. However, it has not been experimentally tested whether receptor heterodimerization is necessary for these additive effects.
E) Within specific cell types, CXCR4, ACKR3, and CXCR4/ACKR3 heterodimers control distinct cell functions. This pattern appears to be a common arrangement of the CXCL12 system in various types of stem and progenitor cells.
{{clear}}

⚫
== References ==
{{reflist}}
{{reflist}}


== External links ==
⚫
==Further reading==
* {{UCSC gene info|ACKR3}}
⚫
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Nagata S, Ishihara T, Robberecht P, ''et al.'' |title=RDC1 may not be VIP receptor. |journal=Trends Pharmacol. Sci. |volume=13 |issue= 3 |pages= 102–3 |year= 1992 |pmid= 1315461 |doi=10.1016/0165-6147(92)90037-7 }}
*{{cite journal | author=Libert F, Passage E, Parmentier M, ''et al.'' |title=Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptor. |journal=Genomics |volume=11 |issue= 1 |pages= 225–7 |year= 1992 |pmid= 1662665 |doi=10.1016/0888-7543(91)90125-X }}


⚫
== Further reading ==
*{{cite journal | author=Sreedharan SP, Robichon A, Peterson KE, Goetzl EJ |title=Cloning and expression of the human vasoactive intestinal peptide receptor. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=88 |issue= 11 |pages= 4986–90 |year= 1991 |pmid= 1675791 |doi=10.1073/pnas.88.11.4986 | pmc=51792 }}
⚫
{{refbegin | 2}}
*{{cite journal | author=Law NM, Rosenzweig SA |title=Characterization of the G-protein linked orphan receptor GPRN1/RDC1. |journal=Biochem. Biophys. Res. Commun. |volume=201 |issue= 1 |pages= 458–65 |year= 1994 |pmid= 8198609 |doi= 10.1006/bbrc.1994.1723 }}
*{{cite journal | author=Shimizu N, Soda Y, Kanbe K, ''et al.'' |title=A putative G protein-coupled receptor, RDC1, is a novel coreceptor for human and simian immunodeficiency viruses. |journal=J. Virol. |volume=74 |issue= 2 |pages= 619–26 |year= 2000 |pmid= 10623723 |doi=10.1128/JVI.74.2.619-626.2000 | pmc=111581 }}
* {{cite journal | vauthors = Nagata S, Ishihara T, Robberecht P, Libert F, Parmentier M, Christophe J, Vassart G | title = RDC1 may not be VIP receptor | journal = Trends in Pharmacological Sciences | volume = 13 | issue = 3 | pages = 102–103 | date = March 1992 | pmid = 1315461 | doi = 10.1016/0165-6147(92)90037-7 }}
*{{cite journal | author=Broberg K, Zhang M, Strömbeck B, ''et al.'' |title=Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15. |journal=Int. J. Oncol. |volume=21 |issue= 2 |pages= 321–6 |year= 2003 |pmid= 12118328 |doi= }}
* {{cite journal | vauthors = Libert F, Passage E, Parmentier M, Simons MJ, Vassart G, Mattei MG | title = Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptor | journal = Genomics | volume = 11 | issue = 1 | pages = 225–227 | date = September 1991 | pmid = 1662665 | doi = 10.1016/0888-7543(91)90125-X }}
*{{cite journal | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 }}
* {{cite journal | vauthors = Sreedharan SP, Robichon A, Peterson KE, Goetzl EJ | title = Cloning and expression of the human vasoactive intestinal peptide receptor | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 88 | issue = 11 | pages = 4986–4990 | date = June 1991 | pmid = 1675791 | pmc = 51792 | doi = 10.1073/pnas.88.11.4986 | doi-access = free | bibcode = 1991PNAS...88.4986S }}
*{{cite journal | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 }}
* {{cite journal | vauthors = Law NM, Rosenzweig SA | title = Characterization of the G-protein linked orphan receptor GPRN1/RDC1 | journal = Biochemical and Biophysical Research Communications | volume = 201 | issue = 1 | pages = 458–465 | date = May 1994 | pmid = 8198609 | doi = 10.1006/bbrc.1994.1723 }}
*{{cite journal | author=Hillier LW, Graves TA, Fulton RS, ''et al.'' |title=Generation and annotation of the DNA sequences of human chromosomes 2 and 4. |journal=Nature |volume=434 |issue= 7034 |pages= 724–31 |year= 2005 |pmid= 15815621 |doi= 10.1038/nature03466 }}
* {{cite journal | vauthors = Shimizu N, Soda Y, Kanbe K, Liu HY, Mukai R, Kitamura T, Hoshino H | title = A putative G protein-coupled receptor, RDC1, is a novel coreceptor for human and simian immunodeficiency viruses | journal = Journal of Virology | volume = 74 | issue = 2 | pages = 619–626 | date = January 2000 | pmid = 10623723 | pmc = 111581 | doi = 10.1128/JVI.74.2.619-626.2000 }}
*{{cite journal | author=Infantino S, Moepps B, Thelen M |title=Expression and regulation of the orphan receptor RDC1 and its putative ligand in human dendritic and B cells. |journal=J. Immunol. |volume=176 |issue= 4 |pages= 2197–207 |year= 2006 |pmid= 16455976 |doi= }}
* {{cite journal | vauthors = Broberg K, Zhang M, Strömbeck B, Isaksson M, Nilsson M, Mertens F, Mandahl N, Panagopoulos I | display-authors = 6 | title = Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15 | journal = International Journal of Oncology | volume = 21 | issue = 2 | pages = 321–326 | date = August 2002 | pmid = 12118328 | doi = 10.3892/ijo.21.2.321 }}
*{{cite journal | author=Burns JM, Summers BC, Wang Y, ''et al.'' |title=A novel chemokine receptor for SDF-1 and I-TAC involved in cell survival, cell adhesion, and tumor development. |journal=J. Exp. Med. |volume=203 |issue= 9 |pages= 2201–13 |year= 2006 |pmid= 16940167 |doi= 10.1084/jem.20052144 | pmc=2118398 }}
* {{cite journal | vauthors = Infantino S, Moepps B, Thelen M | title = Expression and regulation of the orphan receptor RDC1 and its putative ligand in human dendritic and B cells | journal = Journal of Immunology | volume = 176 | issue = 4 | pages = 2197–2207 | date = February 2006 | pmid = 16455976 | doi = 10.4049/jimmunol.176.4.2197 | doi-access = free }}
*{{cite journal | author=Proost P, Mortier A, Loos T, ''et al.'' |title=Proteolytic processing of CXCL11 by CD13/aminopeptidase N impairs CXCR3 and CXCR7 binding and signaling and reduces lymphocyte and endothelial cell migration. |journal=Blood |volume=110 |issue= 1 |pages= 37–44 |year= 2007 |pmid= 17363734 |doi= 10.1182/blood-2006-10-049072 }}
* {{cite journal | vauthors = Burns JM, Summers BC, Wang Y, Melikian A, Berahovich R, Miao Z, Penfold ME, Sunshine MJ, Littman DR, Kuo CJ, Wei K, McMaster BE, Wright K, Howard MC, Schall TJ | display-authors = 6 | title = A novel chemokine receptor for SDF-1 and I-TAC involved in cell survival, cell adhesion, and tumor development | journal = The Journal of Experimental Medicine | volume = 203 | issue = 9 | pages = 2201–2213 | date = September 2006 | pmid = 16940167 | pmc = 2118398 | doi = 10.1084/jem.20052144 }}
* {{cite journal | vauthors = Proost P, Mortier A, Loos T, Vandercappellen J, Gouwy M, Ronsse I, Schutyser E, Put W, Parmentier M, Struyf S, Van Damme J | display-authors = 6 | title = Proteolytic processing of CXCL11 by CD13/aminopeptidase N impairs CXCR3 and CXCR7 binding and signaling and reduces lymphocyte and endothelial cell migration | journal = Blood | volume = 110 | issue = 1 | pages = 37–44 | date = July 2007 | pmid = 17363734 | doi = 10.1182/blood-2006-10-049072 | doi-access = free }}
}}
*{{cite journal | author=Miao Z, Luker KE, "et al." |title=CXCR7 (RDC1) promotes breast and lung tumor growth in vivo and is expressed on tumor-associated vasculature. |journal=PNAS | volume=104 |pages= 15735–15740 |year=2007 |doi=10.1073/pnas.0610444104 | pmid=17898181 | issue=40 | pmc=1994579}}
* {{cite journal | vauthors = Miao Z, Luker KE, Summers BC, Berahovich R, Bhojani MS, Rehemtulla A, Kleer CG, Essner JJ, Nasevicius A, Luker GD, Howard MC, Schall TJ | display-authors = 6 | title = CXCR7 (RDC1) promotes breast and lung tumor growth in vivo and is expressed on tumor-associated vasculature | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 104 | issue = 40 | pages = 15735–15740 | date = October 2007 | pmid = 17898181 | pmc = 1994579 | doi = 10.1073/pnas.0610444104 | doi-access = free | bibcode = 2007PNAS..10415735M }}
* {{cite journal | vauthors = Boldajipour B, Mahabaleshwar H, Kardash E, Reichman-Fried M, Blaser H, Minina S, Wilson D, Xu Q, Raz E | display-authors = 6 | title = Control of chemokine-guided cell migration by ligand sequestration | journal = Cell | volume = 132 | issue = 3 | pages = 463–473 | date = February 2008 | pmid = 18267076 | doi = 10.1016/j.cell.2007.12.034 | doi-access = free | hdl = 11858/00-001M-0000-0012-DDE5-7 | hdl-access = free }}
*{{cite journal|author=Wang J, Shiozawa Y, Wang J "et al." |title=The role of CXCR7/RDC1 as a chemokine receptor for CXCL12/SDF-1 in prostate cancer. |journal=J Biol Chem |volume=283 |year= 2008 |pages=4283–4294 |doi=10.1074/jbc.M707465200|pmid=18057003|issue=7 }}
*{{cite journal|author=Boldajipour B, Mahabaleshwar H, Kardash E ''et al.'' |title=Control of Chemokine-Guided Cell Migration by Ligand Sequestration. |journal=Cell |volume=132 |year= 2008 |pages=463–473 | pmid=18267076 |doi=10.1016/j.cell.2007.12.034|issue=3}}
* {{cite journal | vauthors = Takaya K, Asou T, Kishi K | title = Selective Elimination of Senescent Fibroblasts by Targeting the Cell Surface Protein ACKR3 | journal = International Journal of Molecular Sciences | volume = 23 | issue = 12 | pages = 6531 | date = June 2022 | pmid = 35742971 | pmc = 9223754 | doi = 10.3390/ijms23126531 | doi-access = free }}
{{refend}}
{{refend}}


{{NLM content}}
{{NLM content}}

{{Chemokine receptors}}
{{Chemokine receptors}}
{{Chemokine receptor modulators}}

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[[Category:Chemokine receptors]]
[[Category:Chemokine receptors]]


{{transmembranereceptor-stub}}

Latest revision as of 03:22, 13 August 2024

ACKR3
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesACKR3, CMKOR1, CXC-R7, CXCR-7, CXCR7, GPR159, RDC-1, RDC1, atypical chemokine receptor 3
External IDsOMIM: 610376; MGI: 109562; HomoloGene: 22419; GeneCards: ACKR3; OMA:ACKR3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

57007

12778

Ensembl

ENSG00000144476

ENSMUSG00000044337

UniProt

P25106

P56485

RefSeq (mRNA)

NM_001047841
NM_020311

NM_001271607
NM_007722

RefSeq (protein)

NP_064707

NP_001258536
NP_031748

Location (UCSC)Chr 2: 236.57 – 236.58 MbChr 1: 90.13 – 90.14 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Atypical chemokine receptor 3 also known as C-X-C chemokine receptor type 7 (CXCR-7) and G-protein coupled receptor 159 (GPR159) is a protein that in humans is encoded by the ACKR3 gene.[5][6]

This gene encodes a G protein-coupled receptor family member. It belongs to the chemokine receptor family of GPCRs. Within this family, ACKR3 is classified as a class A GPCR.[7] This GPCR protein was earlier thought to be a receptor for vasoactive intestinal peptide (VIP) and was considered to be an orphan receptor. It is now classified as a chemokine receptor able to bind the chemokines CXCL12/SDF-1 and CXCL11. The protein is also a coreceptor for human immunodeficiency viruses (HIV). Translocations involving this gene and HMGA2 on chromosome 12 have been observed in lipomas. Alternatively spliced transcript variants encoding the same protein isoform have been found for this gene. Whereas some reports claim that the receptor induces signaling following ligand binding, recent findings in zebrafish suggest that CXCR7 functions primarily by sequestering the chemokine CXCL12.[6]

Another study has provided evidence that ligand binding to CXCR7 activates MAP kinases through Beta-arrestins, and thus has functions beyond ligand sequestration.[8]

ACKR3 has also been shown to sequester endogenous opioid peptides and is thought to modulate their activity.[9]

Nomenclature

[edit]

In 2013, the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology subcommittee for chemokine receptors reevaluated C-X-C chemokine receptor type 7 (CXCR7) and classified it as an atypical chemokine receptor, leading to its renaming as atypical chemokine receptor 3 (ACKR3). Additional names that have been mentioned in the literature, albeit less frequently, include GPR159 and Orphan receptor RDC1, the latter being a term primarily found in older literature.[10]

Function

[edit]

ACKR3 stands out as an atypical receptor due to its β-arrestin-biased signaling nature. In the case of a β-arrestin-biased receptor like ACKR3, when it is treated with an unbiased ligand, it triggers signaling pathways solely mediated by β-arrestin. What sets ACKR3 apart is its absence of G-protein involvement, which distinguishes it from typical GPCRs.[11]

Despite being considered atypical, the functions of ACKR3 do not imply that it acts as a completely inactive receptor for CXCL12. On the contrary, extensive literature supports the notion of ACKR3 engaging in active signaling, which is believed to rely on arrestin-mediated mechanisms. Nevertheless, its role as a decoy receptor for CXCL12/SDF1 is well-established. This is evident by the significantly higher affinity of CXCL12 binding to ACKR3/CXCR7 compared to CXCR4, along with its constant internalization facilitated by the recruitment of β-arrestin, without known downstream signaling events.[12][13]

Ligands

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In addition to CXCL12, ACKR3 engages with multiple ligands, encompassing CXCL11, macrophage inhibitory factor (MIF), adrenomedullin (ADM), opioid peptides such as nociceptin, dynorphin, and enkephalin, as well as the viral chemokine vCCL2/viral macrophage inflammatory protein-II. [12][14]

Inhibition of ACKR3 by ligands such as the peptide LIH383 (FGGFMRRK-NH2) and the small molecules conolidine, RTI-5152-12, and VUF15485 increases opioid peptide activity and produces analgesic and antidepressant effects in animal studies.[9][15][16]

Interactions

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ACKR3 and CXCR4 have been shown to interact, different possibilities regarding the involvement of ACKR3 and CXCR4 in CXCL12 signaling:[12]

A) ACKR3 can attenuate CXCR4 signaling by forming heterodimers with CXCR4. While this interaction was initially observed in cells with CXCR7 overexpression, it has rarely been observed with endogenous CXCR7.

B) Multiple cell types demonstrate that either ACKR3 or CXCR4 controls specific cell functions (e.g., migration, proliferation). The distinct regulation of these functions occurs through one of the receptors.

C) Synergistic effects between CXCR4 and ACKR3 have been observed in many cases, suggesting that cellular responses to CXCL12 require the presence of both receptors. Whether receptor heterodimerization is responsible for these synergistic effects remains uncertain.

D) In addition to synergistic effects, a few studies have shown additive effects of ACKR3 and CXCR4 on specific cell functions. However, it has not been experimentally tested whether receptor heterodimerization is necessary for these additive effects. E) Within specific cell types, CXCR4, ACKR3, and CXCR4/ACKR3 heterodimers control distinct cell functions. This pattern appears to be a common arrangement of the CXCL12 system in various types of stem and progenitor cells.

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000144476 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000044337 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Balabanian K, Lagane B, Infantino S, Chow KY, Harriague J, Moepps B, et al. (October 2005). "The chemokine SDF-1/CXCL12 binds to and signals through the orphan receptor RDC1 in T lymphocytes". The Journal of Biological Chemistry. 280 (42): 35760–35766. doi:10.1074/jbc.M508234200. PMID 16107333.
  6. ^ a b "Entrez Gene: CXCR7 chemokine (C-X-C motif) receptor 7".
  7. ^ Fumagalli A, Zarca A, Neves M, Caspar B, Hill SJ, Mayor F, et al. (December 2019). "CXCR4/ACKR3 Phosphorylation and Recruitment of Interacting Proteins: Key Mechanisms Regulating Their Functional Status". Molecular Pharmacology. 96 (6): 794–808. doi:10.1124/mol.118.115360. hdl:10261/214032. PMID 30837297. S2CID 73513931.
  8. ^ * Rajagopal S, Kim J, Ahn S, Craig S, Lam CM, Gerard NP, et al. (January 2010). "Beta-arrestin- but not G protein-mediated signaling by the "decoy" receptor CXCR7". Proceedings of the National Academy of Sciences of the United States of America. 107 (2): 628–632. Bibcode:2010PNAS..107..628R. doi:10.1073/pnas.0912852107. PMC 2818968. PMID 20018651.
  9. ^ a b Meyrath M, Szpakowska M, Zeiner J, Massotte L, Merz MP, Benkel T, et al. (June 2020). "The atypical chemokine receptor ACKR3/CXCR7 is a broad-spectrum scavenger for opioid peptides". Nature Communications. 11 (1): 3033. Bibcode:2020NatCo..11.3033M. doi:10.1038/s41467-020-16664-0. PMC 7305236. PMID 32561830.
  10. ^ Bachelerie F, Graham GJ, Locati M, Mantovani A, Murphy PM, Nibbs R, et al. (March 2014). "New nomenclature for atypical chemokine receptors". Nature Immunology. 15 (3): 207–208. doi:10.1038/ni.2812. PMID 24549061. S2CID 205367583.
  11. ^ Rajagopal S, Kim J, Ahn S, Craig S, Lam CM, Gerard NP, et al. (January 2010). "Beta-arrestin- but not G protein-mediated signaling by the "decoy" receptor CXCR7". Proceedings of the National Academy of Sciences of the United States of America. 107 (2): 628–632. Bibcode:2010PNAS..107..628R. doi:10.1073/pnas.0912852107. PMC 2818968. PMID 20018651.
  12. ^ a b c Koch C, Engele J (November 2020). "Functions of the CXCL12 Receptor ACKR3/CXCR7-What Has Been Perceived and What Has Been Overlooked". Molecular Pharmacology. 98 (5): 577–585. doi:10.1124/molpharm.120.000056. PMID 32883765. S2CID 221498026.
  13. ^ Pance K, Gramespacher JA, Byrnes JR, Salangsang F, Serrano JC, Cotton AD, et al. (February 2023). "Modular cytokine receptor-targeting chimeras for targeted degradation of cell surface and extracellular proteins". Nature Biotechnology. 41 (2): 273–281. doi:10.1038/s41587-022-01456-2. PMC 9931583. PMID 36138170.
  14. ^ Meyrath M, Szpakowska M, Zeiner J, Massotte L, Merz MP, Benkel T, et al. (June 2020). "The atypical chemokine receptor ACKR3/CXCR7 is a broad-spectrum scavenger for opioid peptides". Nature Communications. 11 (1): 3033. Bibcode:2020NatCo..11.3033M. doi:10.1038/s41467-020-16664-0. PMC 7305236. PMID 32561830.
  15. ^ Szpakowska M, Decker AM, Meyrath M, Palmer CB, Blough BE, Namjoshi OA, Chevigné A (June 2021). "The natural analgesic conolidine targets the newly identified opioid scavenger ACKR3/CXCR7". Signal Transduct Target Ther. 6 (1): 209. doi:10.1038/s41392-021-00548-w. PMC 8169647. PMID 34075018.
  16. ^ Zarca AM, Adlere I, Viciano CP, Arimont-Segura M, Meyrath M, Simon IA, Bebelman JP, Laan D, Custers HG, Janssen E, Versteegh KL, Buzink MC, Nesheva DN, Bosma R, de Esch IJ, Vischer HF, Wijtmans M, Szpakowska M, Chevigné A, Hoffmann C, de Graaf C, Zarzycka BA, Windhorst AD, Smit MJ, Leurs R (March 2024). "Pharmacological Characterization and Radiolabeling of VUF15485, a High-Affinity Small-Molecule Agonist for the Atypical Chemokine Receptor ACKR3" (PDF). Mol Pharmacol. 105 (4): 301–312. doi:10.1124/molpharm.123.000835. PMID 38346795.
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Further reading

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This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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