Signaling lymphocytic activation molecule

Members of the family include:

• SLAMF1 (CD150)
• SLAMF2 (CD48, FimH){{cite journal | vauthors = Sintes J, Engel P | title = SLAM (CD150) is a multitasking immunoreceptor: from cosignalling to bacterial recognition | journal = Immunology and Cell Biology | volume = 89 | issue = 2 | pages = 161–3 | date = February 2011 | pmid = 21102539 | doi = 10.1038/icb.2010.145 | doi-access = | s2cid = 31409234 }}
• SLAMF3 (CD229, LY9)
• SLAMF4 (CD244, 2B4)
• SLAMF5 (CD84)
• SLAMF6 (CD352){{cite journal | vauthors = Chatterjee M, Kis-Toth K, Thai TH, Terhorst C, Tsokos GC | title = SLAMF6-driven co-stimulation of human peripheral T cells is defective in SLE T cells | journal = Autoimmunity | volume = 44 | issue = 3 | pages = 211–8 | date = May 2011 | pmid = 21231893 | pmc = 4465387 | doi = 10.3109/08916934.2010.530627 }}

• SLAMF7 (CD319, CRACC){{cite journal | vauthors = Kim JR, Horton NC, Mathew SO, Mathew PA | title = CS1 (SLAMF7) inhibits production of proinflammatory cytokines by activated monocytes | journal = Inflammation Research | volume = 62 | issue = 8 | pages = 765–72 | date = August 2013 | pmid = 23695528 | doi = 10.1007/s00011-013-0632-1 | s2cid = 11918450 }}
• SLAMF8 (CD353){{cite journal | vauthors = Wang G, Abadía-Molina AC, Berger SB, Romero X, O'Keeffe MS, Rojas-Barros DI, Aleman M, Liao G, Maganto-García E, Fresno M, Wang N, Detre C, Terhorst C | title = Cutting edge: Slamf8 is a negative regulator of Nox2 activity in macrophages | journal = Journal of Immunology | volume = 188 | issue = 12 | pages = 5829–32 | date = June 2012 | pmid = 22593622 | pmc = 3370125 | doi = 10.4049/jimmunol.1102620 }}
• SLAMF9{{cite journal | vauthors = Pott S, Kamrani NK, Bourque G, Pettersson S, Liu ET | title = PPARG binding landscapes in macrophages suggest a genome-wide contribution of PU.1 to divergent PPARG binding in human and mouse | journal = PLOS ONE | volume = 7 | issue = 10 | pages = e48102 | year = 2012 | pmid = 23118933 | pmc = 3485280 | doi = 10.1371/journal.pone.0048102 | bibcode = 2012PLoSO...748102P | editor1-last = Jothi | editor1-first = Raja | doi-access = free }}

SLAMFs are CD2-related surface receptors expressed by activated B and T cells, natural killer (NK) cells, dendritic cells, macrophages, eosinophils, neutrophils, and platelets, although different SLAMF receptors have varying expression patterns. SLAMF receptors are cell surface transmembrane molecules that can interact directly with microbes, which can cause phagocytic cells to migrate to the area.{{Cite journal|last1=van Driel|first1=Boaz Job|last2=Liao|first2=Gongxian|last3=Engel|first3=Pablo|last4=Terhorst|first4=Cox|date=2016-01-20|title=Responses to Microbial Challenges by SLAMF Receptors|journal=Frontiers in Immunology|volume=7|page=4|doi=10.3389/fimmu.2016.00004|issn=1664-3224|pmc=4718992|pmid=26834746|doi-access=free}} SLAMF1 and SLAMF6 are known to directly interact with outer membrane porins on gram negative bacteria. SLAMF1 is a known receptor for the measles virus and also serves as an opsonin for phagocytic cells, enhancing phagocytosis by localizing to phagosomes and inducing a signaling cascade resulting in enhanced fusion of phagosomes and lysosomes.{{Cite journal|last1=Detre|first1=Cynthia|last2=Keszei|first2=Marton|last3=Romero|first3=Xavier|last4=Tsokos|first4=George C.|last5=Terhorst|first5=Cox|date=2010-06-01|title=SLAM family receptors and the SLAM-associated protein (SAP) modulate T cell functions|journal=Seminars in Immunopathology|language=en|volume=32|issue=2|pages=157–171|doi=10.1007/s00281-009-0193-0|issn=1863-2300|pmc=2868096|pmid=20146065}} SLAMF2 is known bind gram negative bacteria and is internalized after binding, promoting phagocytosis. SLAMFs are also involved in immune cell communication; SLAMFs are co-stimulatory molecules for both T-cells and NK cells. SLAMs enhance T helper cell proliferation by increasing IFN-gamma and IL-4 production.

File:SLAM_signaling.png

All members of the SLAMF family are classified as type I glycoproteins and share an amino-terminal IgV variable domain and a membrane-adjacent IgC2 constant domain, along with immunoreceptor tyrosine-based switch motifs (ITSMs).{{Cite journal|last1=Cannons|first1=Jennifer L.|last2=Tangye|first2=Stuart G.|last3=Schwartzberg|first3=Pamela L.|date=2011-04-23|title=SLAM Family Receptors and SAP Adaptors in Immunity|journal=Annual Review of Immunology|language=en|volume=29|issue=1|pages=665–705|doi=10.1146/annurev-immunol-030409-101302|pmid=21219180|issn=0732-0582}} The IgV and IgC2 domains are located on the extracellular portion of the receptor, while the ITSMs are used for signaling within the cell. SLAMFs can undergo alternative splicing, which can generate different isoforms of the SLAMF molecules that have different numbers of ITSMs and tyrosines, potentially with different functions. Proteins with SH2 domains are able to bind these ITSMs to initiate signaling cascades within the cell. SLAMF2 and SLAMF4 interact with one another, but all other SLAMF receptors are self-ligands, meaning that they interact with the corresponding receptor on other cells in a homophilic way.

SLAMFs are potential targets for immunotherapy. For example, elotuzumab is an anti-SLAMF7 humanized monoclonal antibody used to treat multiple myeloma. SLAMF7 is a self-ligand over-expressed in plasma cells of multiple myeloma patients. Elotuzumab stimulates NK cells to release granzyme through blocking SLAMF7, through triggering antibody-dependent cellular cytotoxicity (ADCC), and through NK cell activation via Ewing’s sarcoma-associated transcript 2 (EAT-2).{{Cite journal|last1=Ritchie|first1=David|last2=Colonna|first2=Marco|date=May 2018|title=Mechanisms of Action and Clinical Development of Elotuzumab: Development of Elotuzumab in Myeloma|journal=Clinical and Translational Science|language=en|volume=11|issue=3|pages=261–266|doi=10.1111/cts.12532|pmc=5944582|pmid=29272564}} EAT-2 is known to bind to phosphorylated tyrosines on ITSMs and alter cytokine production. Elotuzumab also blocks multiple myeloma cells from interacting with one another via the SLAMF7 ligand.{{Cite journal|last=Sell|first=Stewart|date=June 2017|title=Cancer immunotherapy: Breakthrough or "deja vu, all over again"?|journal=Tumor Biology|language=en|volume=39|issue=6|pages=101042831770776|doi=10.1177/1010428317707764|pmid=28639883|issn=1010-4283|doi-access=free}}

The X-linked SLAM-associated protein (SAP), encoded by the SH2D1A gene, consists primarily of an SH2 domain which can interact with ITSMs present on most SLAMF receptors. Unlike most SH2 binding proteins, SAP does not require tyrosines on the ITSMs to be phosphorylated prior to binding. SAP is expressed in lymphocytes (specifically NK cells and T cells, but not usually B cells), eosinophils, and platelets. A defective SLAM associated protein (SAP) causes X-linked lymphoproliferative syndrome (XLP), a frequently lethal mononucleosis characterized by inability to respond to infection with Epstein-Barr virus (EBV), leading to a failure to clear B-cells infected with the virus, which can be fatal.

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Category:Genes on human chromosome 1

Category:Single-pass transmembrane proteins