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CD47

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CD47
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCD47, IAP, MER6, OA3, CD47 molecule
External IDsOMIM: 601028; MGI: 96617; HomoloGene: 1346; GeneCards: CD47; OMA:CD47 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

961

16423

Ensembl

ENSG00000196776

ENSMUSG00000055447

UniProt

Q08722

Q61735

RefSeq (mRNA)

NM_001025079
NM_001025080
NM_001777
NM_198793
NM_001382306

NM_010581
NM_001368415
NM_001368416
NM_001368417
NM_001368418

RefSeq (protein)

NP_001768
NP_942088
NP_001369235

NP_034711
NP_001355344
NP_001355345
NP_001355346
NP_001355347

Location (UCSC)Chr 3: 108.04 – 108.09 MbChr 16: 49.62 – 49.74 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

CD47 (Cluster of Differentiation 47) also known as integrin associated protein (IAP) is a transmembrane protein that in humans is encoded by the CD47 gene. CD47 belongs to the immunoglobulin superfamily[5] and partners with membrane integrins and also binds the ligands thrombospondin-1 (TSP-1) and signal-regulatory protein alpha (SIRPα).[6] CD-47 acts as a don't eat me signal to macrophages of the immune system which has made it a potential therapeutic target in some cancers, and more recently, for the treatment of pulmonary fibrosis.[7]

CD47 is involved in a range of cellular processes, including apoptosis, proliferation, adhesion, and migration. Furthermore, it plays a role in insulin secretion, as well as immune and angiogenic responses. CD47 is ubiquitously expressed in human cells and has been found to be overexpressed in many different tumor cells.[6][8] Expression in equine cutaneous tumors has been reported as well.[9]

Structure

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CD47 is a 50 kDa membrane receptor that has extracellular N-terminal IgV domain, five transmembrane domains, and a short C-terminal intracellular tail. There are four alternatively spliced isoforms of CD47 that differ only in the length of their cytoplasmic tail.[10]

Form 2 is the most widely expressed form that is found in all circulating and immune cells. The second most abundant isoform is form 4, which is predominantly expressed in the brain and in the peripheral nervous system. Only keratinocytes expressed significant amounts of form 1. Little is known about the functional significance of this alternative splicing. However, these isoforms are highly conserved between mouse and man, suggesting an important role for the cytoplasmic domains in CD47 function.[6][10][11]

Interactions

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Thrombospondin (TSP)

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CD47 is a high affinity receptor for thrombospondin-1 (TSP-1), a secreted glycoprotein that plays a role in vascular development and angiogenesis, and in this later capacity the TSP1-CD47 interaction inhibits nitric oxide signaling at multiple levels in vascular cells.[12] Binding of TSP-1 to CD47 influences several fundamental cellular functions including cell migration and adhesion, cell proliferation or apoptosis, and plays a role in the regulation of angiogenesis and inflammation.[6]

Signal-regulatory protein (SIRP)

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CD47 interacts with signal-regulatory protein alpha (SIRPα), an inhibitory transmembrane receptor present on myeloid cells. The CD47/SIRPα interaction leads to bidirectional signaling, resulting in different cell-to-cell responses including inhibition of phagocytosis, stimulation of cell-cell fusion, and T-cell activation.[6][13][14]

Integrins

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CD47 interacts with several membrane integrins, most commonly integrin αVβ3. These interactions result in CD47/integrin complexes that affect a range of cell functions including adhesion, spreading and migration.[6][14]

Function

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Tumor cells

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Due to the ubiquitous expression of CD47, signaling differs according to cell type. It is likely that intracellular and membrane-associated partners are crucial in determining the cellular response of CD47 signaling.

Cell proliferation

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The role of CD47 in promoting cell proliferation is heavily dependent on cell type as both activation and loss of CD47 can result in enhanced proliferation.

Activation of CD47 with TSP-1 increases proliferation of human U-87 MG and U373 astrocytoma cells but not normal astrocytes. Additionally, CD47 blocking antibodies inhibit proliferation of unstimulated astrocytoma cells but not normal astrocytes. Though the exact mechanism is unclear, it is likely that CD47 promotes proliferation via the PI3K/Akt pathway in cancerous cells but not normal cells.[15]

Loss of CD47 allows sustained proliferation of primary murine endothelial cells and enables these cells to spontaneously reprogram to form multipotent embryoid body-like clusters. Expression of several stem cell markers, including c-Myc, is elevated in CD47-null endothelial cells and a human T cell line lacking CD47. Activation of CD47 with TSP-1 in wild-type cells inhibits proliferation and reduces expression of stem cell transcription factors.[16]

Cell death

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CD47 ligation leads to cell death in many normal and tumor cell lines via apoptosis or autophagy. The activation of CD47 induces rapid apoptosis of T cells. Jurkat cells and peripheral blood mononuclear cells (PBMC) incubated with the monoclonal antibody Ad22 results in apoptosis within 3 hours. However, apoptosis was not observed following culture with other anti-CD47 antibodies. The apoptosis inducing function of CD47 appears to be dependent on activation of specific epitopes on the extracellular domain.[17]

Similarly, CD47 ligation rapidly induces apoptosis in B-cell chronic lymphocytic leukemia (CLL) cells. Treatment with a disulfide-linked antibody dimer induces apoptosis of CD47-positive primary B-CLL and leukemic cells (MOLT-4 and JOK-1). In addition, administration of the antibody prolonged survival of SCID mice implanted with JOK-1 cells. Apoptosis induction appears to be regulated by the hypoxia inducible factor 1α (HIF-1α) pathway.[18]

The RAS-transformed cell lines MDFB6 and B6ras show near complete loss of TSP-1 expression. Activation of CD47 with TSP-1 results in loss of viability in these RAS-expressing cells. Affected cells do not exhibit hallmarks of apoptosis but rather autophagy as seen by staining with acridine orange and immunoreactivity for LC3.[19]

Migration

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Cell migration appears to be universally stimulated by CD47 ligation and activation. The role of CD47 in cell migration was first demonstrated for neutrophils, where CD47 blocking antibodies inhibited transmigration of neutrophils and monocytes through the endothelium. These effects were shown to be dependent on avb3 integrins, which interact with and are activated by CD47 at the plasma membrane.[6][14]

Originally discovered by Irving Weissman’s group at Stanford University, blocking CD47 function has been shown to inhibit migration and metastasis in a variety of tumor models. Blockade of CD47 by neutralizing antibodies reduced migration and chemotaxis in response to collagen IV in melanoma, prostate cancer and ovarian cancer-derived cells.[20] In a mouse model of multiple myeloma, tumor metastasis to bone was decreased in CD47-deficient mice compared with wild type controls.[21] In work led by Mark Chao and Ash Alizadeh, at Stanford, mice were xenografted with human non-Hodgkin lymphoma (NHL) cells; blocking CD47 function with shRNA or antibodies led to a dramatic reduction in metastasis to major organs.[22]

Stromal cells

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Angiogenesis

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Loss of CD47 promotes proliferation and increases asymmetric division of primary murine endothelial cells.[16] Additionally, activation of CD47 with TSP-1 in wild-type primary mouse cerebral endothelial cells induces cytotoxicity, which is significantly decreased in cerebral endothelial cells derived from CD47 knockout mice.[23]

CD47 signaling may suppress angiogenesis as TSP-1 activation significantly inhibited endothelial cell migration and tube formation in vitro.[23] In vivo, injections of TSP-1 in mice after hindlimb ischemia induces a significant decrease of blood flow recovery.[24] The mechanism of the anti-angiogenic activity of CD47 is not fully understood, but introduction of CD47 antibodies and TSP-1 have been shown to inhibit nitric oxide (NO)-stimulated responses in both endothelial and vascular smooth muscle cells.[12] CD47 signaling influences the SDF-1 chemokine pathway, which plays a role in angiogenesis.[24]

Inflammatory response

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Interactions between endothelial cell CD47 and leukocyte SIRPγ regulate T cell transendothelial migration (TEM) at sites of inflammation. CD47 knockout mice show reduced recruitment of blood T cells as well as neutrophils and monocytes in areas of inflammation.[25] CD47 also functions as a marker of self on murine red blood cells which allows RBC to avoid phagocytosis. Red blood cells that lack CD47 are rapidly cleared from the bloodstream by macrophages, a process that is mediated by interaction with SIRPα.[26] Mouse hematopoietic stem cells (HSCs) and progenitors transiently upregulate CD47 during their migratory phase, which reduces macrophage engulfment in vivo.[27]

Tumor cells can also evade macrophage phagocytosis through the expression of CD47.[8] CD47 is highly expressed in bladder tumor initiating cells (T-ICs) compared with the rest of the tumor. Blockade of CD47 with a monoclonal antibody results in macrophage engulfment of bladder cancer cells in vitro.[28] CD47 is also upregulated in mouse and human myeloid leukemias, and overexpression of CD47 on a myeloid leukemia line allows these cells to evade phagocytosis.[27]

Insulin secretion

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CD47 receptor signaling inhibits insulin release from human as well as mouse pancreatic β cells and that it can be pharmacologically blocked to boost insulin secretion in both models.[29]

Clinical significance

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CD47 was first identified as a tumor antigen on human ovarian cancer in the 1980s. Since then, CD47 has been found to be expressed on multiple human tumor types including acute myeloid leukemia (AML), chronic myeloid leukemia, acute lymphoblastic leukemia (ALL), non-Hodgkin's lymphoma (NHL), multiple myeloma (MM), bladder cancer, and other solid tumors.[8] CD47 is also highly expressed on pediatric and adult brain tumors.[30]

High levels of CD47 allows cancer cells to avoid phagocytosis despite having a higher level of calreticulin - the dominant pro-phagocytic signal.[31] This is due to engagement of the SIRP-α of macrophage by CD47. Engagement of SIRP-α leads to inhibition of phagocytosis. Thus blocking CD47 with antibody turns off “don’t eat me” signal and favors phagocytosis.

As a potential drug target

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Anti-CD47 antibody–mediated phagocytosis of cancer fosters the activation of cancer-specific lymphocytes: cancer cells display mutant proteins to which the immune system can now react.[32][33] Based on significant activity in preclinical models and in synergistic combinations with other antibodies,[34] Humanized anti-CD47 antibody is being evaluated for the treatment of various cancers, e.g. diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL)[35] , Primary Effusion Lymphoma[36] and acute myeloid leukemia (AML).[37]

See also

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References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000196776 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000055447 – 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. ^ "Entrez Gene: CD47 CD47 molecule".
  6. ^ a b c d e f g Sick E, Jeanne A, Schneider C, Dedieu S, Takeda K, Martiny L (December 2012). "CD47 update: a multifaceted actor in the tumour microenvironment of potential therapeutic interest". British Journal of Pharmacology. 167 (7): 1415–1430. doi:10.1111/j.1476-5381.2012.02099.x. PMC 3514757. PMID 22774848.
  7. ^ "Fibrosis reversed when 'don't eat me' signal blocked, study finds". medicalxpress.com.
  8. ^ a b c Chao MP, Weissman IL, Majeti R (April 2012). "The CD47-SIRPα pathway in cancer immune evasion and potential therapeutic implications". Current Opinion in Immunology. 24 (2): 225–232. doi:10.1016/j.coi.2012.01.010. PMC 3319521. PMID 22310103.
  9. ^ Caston SS, Cooper EE, Chandramani-Shivalingappa P, Sponseller BA, Hostetter JM, Sun Y (July 2016). "CD47 expression in cryopreserved equine cutaneous masses and normal skin". Journal of Veterinary Diagnostic Investigation. 28 (4): 408–413. doi:10.1177/1040638716643352. PMID 27154320.
  10. ^ a b Reinhold MI, Lindberg FP, Plas D, Reynolds S, Peters MG, Brown EJ (November 1995). "In vivo expression of alternatively spliced forms of integrin-associated protein (CD47)". Journal of Cell Science. 108 ( Pt 11) (Pt 11): 3419–3425. doi:10.1242/jcs.108.11.3419. PMID 8586654.
  11. ^ Frazier WA, Isenberg JS, Kaur S, Roberts DD (February 2010). "CD47". UCSD Nature Molecule Pages. doi:10.1038/mp.a002870.01 (inactive 2024-11-02).{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)
  12. ^ a b Isenberg JS, Ridnour LA, Dimitry J, Frazier WA, Wink DA, Roberts DD (September 2006). "CD47 is necessary for inhibition of nitric oxide-stimulated vascular cell responses by thrombospondin-1". The Journal of Biological Chemistry. 281 (36): 26069–26080. doi:10.1074/jbc.M605040200. PMID 16835222.
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  16. ^ a b Kaur S, Soto-Pantoja DR, Stein EV, Liu C, Elkahloun AG, Pendrak ML, et al. (April 2013). "Thrombospondin-1 signaling through CD47 inhibits self-renewal by regulating c-Myc and other stem cell transcription factors". Scientific Reports. 3: 1673. Bibcode:2013NatSR...3.1673K. doi:10.1038/srep01673. PMC 3628113. PMID 23591719.
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  18. ^ Sagawa M, Shimizu T, Fukushima N, Kinoshita Y, Ohizumi I, Uno S, et al. (June 2011). "A new disulfide-linked dimer of a single-chain antibody fragment against human CD47 induces apoptosis in lymphoid malignant cells via the hypoxia inducible factor-1α pathway". Cancer Science. 102 (6): 1208–1215. doi:10.1111/j.1349-7006.2011.01925.x. PMID 21401803. S2CID 205236897.
  19. ^ Kalas W, Swiderek E, Switalska M, Wietrzyk J, Rak J, Strzadala L (April 2013). "Thrombospondin-1 receptor mediates autophagy of RAS-expressing cancer cells and triggers tumour growth inhibition". Anticancer Research. 33 (4): 1429–1438. PMID 23564783.
  20. ^ Shahan TA, Fawzi A, Bellon G, Monboisse JC, Kefalides NA (February 2000). "Regulation of tumor cell chemotaxis by type IV collagen is mediated by a Ca(2+)-dependent mechanism requiring CD47 and the integrin alpha(V)beta(3)". The Journal of Biological Chemistry. 275 (7): 4796–4802. doi:10.1074/jbc.275.7.4796. PMID 10671513.
  21. ^ Uluçkan O, Becker SN, Deng H, Zou W, Prior JL, Piwnica-Worms D, et al. (April 2009). "CD47 regulates bone mass and tumor metastasis to bone". Cancer Research. 69 (7): 3196–3204. doi:10.1158/0008-5472.CAN-08-3358. PMC 2763641. PMID 19276363.
  22. ^ Chao MP, Tang C, Pachynski RK, Chin R, Majeti R, Weissman IL (November 2011). "Extranodal dissemination of non-Hodgkin lymphoma requires CD47 and is inhibited by anti-CD47 antibody therapy". Blood. 118 (18): 4890–4901. doi:10.1182/blood-2011-02-338020. PMC 3208297. PMID 21828138.
  23. ^ a b Xing C, Lee S, Kim WJ, Wang H, Yang YG, Ning M, et al. (August 2009). "Neurovascular effects of CD47 signaling: promotion of cell death, inflammation, and suppression of angiogenesis in brain endothelial cells in vitro". Journal of Neuroscience Research. 87 (11): 2571–2577. doi:10.1002/jnr.22076. PMC 3712846. PMID 19360900.
  24. ^ a b Smadja DM, d'Audigier C, Bièche I, Evrard S, Mauge L, Dias JV, et al. (March 2011). "Thrombospondin-1 is a plasmatic marker of peripheral arterial disease that modulates endothelial progenitor cell angiogenic properties". Arteriosclerosis, Thrombosis, and Vascular Biology. 31 (3): 551–559. doi:10.1161/ATVBAHA.110.220624. PMID 21148423.
  25. ^ Azcutia V, Stefanidakis M, Tsuboi N, Mayadas T, Croce KJ, Fukuda D, et al. (September 2012). "Endothelial CD47 promotes vascular endothelial-cadherin tyrosine phosphorylation and participates in T cell recruitment at sites of inflammation in vivo". Journal of Immunology. 189 (5): 2553–2562. doi:10.4049/jimmunol.1103606. PMC 3424398. PMID 22815286.
  26. ^ Oldenborg PA, Zheleznyak A, Fang YF, Lagenaur CF, Gresham HD, Lindberg FP (June 2000). "Role of CD47 as a marker of self on red blood cells". Science. 288 (5473): 2051–2054. Bibcode:2000Sci...288.2051O. doi:10.1126/science.288.5473.2051. PMID 10856220.
  27. ^ a b Jaiswal S, Jamieson CH, Pang WW, Park CY, Chao MP, Majeti R, et al. (July 2009). "CD47 is upregulated on circulating hematopoietic stem cells and leukemia cells to avoid phagocytosis". Cell. 138 (2): 271–285. doi:10.1016/j.cell.2009.05.046. PMC 2775564. PMID 19632178.
  28. ^ Chan KS, Espinosa I, Chao M, Wong D, Ailles L, Diehn M, et al. (August 2009). "Identification, molecular characterization, clinical prognosis, and therapeutic targeting of human bladder tumor-initiating cells". Proceedings of the National Academy of Sciences of the United States of America. 106 (33): 14016–14021. Bibcode:2009PNAS..10614016C. doi:10.1073/pnas.0906549106. PMC 2720852. PMID 19666525.
  29. ^ Ghimire K, Kale A, Li J, Julovi SM, O'Connell P, Grey ST, et al. (October 2023). "A metabolic role for CD47 in pancreatic β cell insulin secretion and islet transplant outcomes". Science Translational Medicine. 15 (717): eadd2387. doi:10.1126/scitranslmed.add2387. PMID 37820008. S2CID 263832103.
  30. ^ Gholamin S, Mitra SS, Feroze AH, Liu J, Kahn SA, Zhang M, et al. (March 2017). "Disrupting the CD47-SIRPα anti-phagocytic axis by a humanized anti-CD47 antibody is an efficacious treatment for malignant pediatric brain tumors". Science Translational Medicine. 9 (381): eaaf2968. doi:10.1126/scitranslmed.aaf2968. PMID 28298418. S2CID 13766254.
  31. ^ Chao MP, Jaiswal S, Weissman-Tsukamoto R, Alizadeh AA, Gentles AJ, Volkmer J, et al. (December 2010). "Calreticulin is the dominant pro-phagocytic signal on multiple human cancers and is counterbalanced by CD47". Science Translational Medicine. 2 (63): 63ra94. doi:10.1126/scitranslmed.3001375. PMC 4126904. PMID 21178137.
  32. ^ Tseng D, Volkmer JP, Willingham SB, Contreras-Trujillo H, Fathman JW, Fernhoff NB, et al. (July 2013). "Anti-CD47 antibody-mediated phagocytosis of cancer by macrophages primes an effective antitumor T-cell response". Proceedings of the National Academy of Sciences of the United States of America. 110 (27): 11103–11108. Bibcode:2013PNAS..11011103T. doi:10.1073/pnas.1305569110. PMC 3703977. PMID 23690610.
  33. ^ Unanue ER (July 2013). "Perspectives on anti-CD47 antibody treatment for experimental cancer". Proceedings of the National Academy of Sciences of the United States of America. 110 (27): 10886–10887. Bibcode:2013PNAS..11010886U. doi:10.1073/pnas.1308463110. PMC 3704033. PMID 23784781.
  34. ^ Chao MP, Alizadeh AA, Tang C, Myklebust JH, Varghese B, Gill S, et al. (September 2010). "Anti-CD47 antibody synergizes with rituximab to promote phagocytosis and eradicate non-Hodgkin lymphoma". Cell. 142 (5): 699–713. doi:10.1016/j.cell.2010.07.044. PMC 2943345. PMID 20813259.
  35. ^ Furlow B (December 2018). "Researchers Report Early Clinical Promise for Macrophage Checkpoint Blockade". Cancer Therapy Advisor. Haymarket Media, Inc.
  36. ^ Goto H, Kojima Y, Matsuda K, Kariya R, Taura M, Kuwahara K, et al. (July 2014). "Efficacy of anti-CD47 antibody-mediated phagocytosis with macrophages against primary effusion lymphoma". European Journal of Cancer. 50 (10): 1836–1846. doi:10.1016/j.ejca.2014.03.004. ISSN 0959-8049. PMID 24726056.
  37. ^ Molica M, Perrone S, Andriola C, Rossi M (October 2023). "Immunotherapy with Monoclonal Antibodies for Acute Myeloid Leukemia: A Work in Progress". Cancers. 15 (20): 5060. doi:10.3390/cancers15205060. PMC 10605302. PMID 37894427.

Further reading

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