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Complement receptor

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Protein family
Complement receptor
Identifiers
SymbolComplement receptor
Membranome116

Acomplement receptor is a membrane-boundreceptor belonging to thecomplement system, which is part of theinnate immune system. Complement receptors bindeffectorprotein fragments that are produced in response to antigen-antibody complexes or damage-associated molecules.[1] Complement receptor activation contributes to the regulation ofinflammation,leukocyte extravasation, andphagocytosis; it also contributes to theadaptive immune response.[2][3] Different complement receptors can participate in either theclassical complement pathway, thealternative complement pathway, or both.[4]

Expression and function

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White blood cells, particularlymonocytes andmacrophages,express complement receptors on their surface. All four complement receptors can bind to fragments ofcomplement component 3 orcomplement component 4 coated on pathogen surface, but the receptors trigger different downstream activities.[1] Complement receptor (CR) 1, 3, and 4 function asopsonins which stimulatephagocytosis, whereas CR2 is expressed only onB cells as aco-receptor.

Red blood cells (RBCs) also express CR1, which enables RBCs to carry complement-boundantigen-antibody complexes to theliver andspleen for degradation.[5]

CR #NameMolecular weight (Da, approx.)[1]Ligand[4]CDMajor cell types[4]aMajor activities[1]
CR1Complement receptor 1190,000–250,000C3b, C4b, iC3bCD35B, E, FDC, Mac, M0, PMNImmune complex transport (E); phagocytosis (PMN, Mac); immune adhesion (E); cofactor and decay-acceleration; secondary Epstein-Barr virus receptor
CR2Complement receptor 2145,000C3d, iC3b, C3dg, Epstein-Barr virusCD21B, FDCB cell coactivator, primary Epstein-Barr virus receptor, CD23 receptor
CR3Macrophage-1 antigen or "integrin αMβ2"170,000 α chain + common 95,000 β chainiC3bCD11b+CD18FDC, Mac, M0, PMNLeukocyte adherence, phagocytosis of iC3b-bound particles
CR4Integrin alphaXbeta2 or "p150,95"150,000 α chain + common 95,000 β chainiC3bCD11c+CD18D, Mac, M0, PMNLeukocyte adhesion
C3AR1C3a receptor75,000C3aEndo, MC, PhaCell activation
C5AR1C5a receptor50,000C5aCD88Endo, MC, PhaCell activation, immune polarization, chemotaxis
C5AR2C5a receptor 236,000C5aChemotaxis
a.^ B:B cell. E:erythrocyte. Endo:endothelial cell. D:dendritic cell. FDC:follicular dendritic cell. Mac:macrophage. MC:mast cell. M0:monocyte. Pha:phagocyte. PMN:polymorphonuclear leukocyte.

Clinical significance

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Main articles:Complement system § Role in disease,Classical complement pathway § Clinical significance, andAlternative complement pathway § Role in disease

Deficits in complement receptor expression can cause disease.[6] Mutations in complement receptors which alter receptor function can also increase risk of certain diseases.[1]

See also

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References

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  1. ^abcdeHolers VM (29 January 2014)."Complement and its receptors: new insights into human disease".Annual Review of Immunology.32:433–59.doi:10.1146/annurev-immunol-032713-120154.PMID 24499275.
  2. ^Verschoor A, Kemper C, Köhl J (15 September 2017). "Complement Receptors".Encyclopedia of Life Sciences. pp. 1–17.doi:10.1002/9780470015902.a0000512.pub3.ISBN 9780470015902.
  3. ^Carroll MC (December 2008)."Complement and humoral immunity".Vaccine.26 (Suppl 8): I28-33.doi:10.1016/j.vaccine.2008.11.022.PMC 4018718.PMID 19388161.
  4. ^abcJaneway Jr CA, Travers P, Walport M, Shlomchik MJ (2001). "The complement system and innate immunity".Immunobiology: The Immune System in Health and Disease (5th ed.). New York: Garland Science. Retrieved17 June 2020.
  5. ^Parham P (2005).The Immune System (2nd ed.). Garland Science.ISBN 9780815340935.
  6. ^Schwartz RA, Thomas I."Complement Receptor Deficiency: eMedicine Dermatology".Medscape. Retrieved7 December 2010.

External links

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Pathways
Activators/enzymes
Early
Middle
Late
Inhibitors
Complement receptors
Function
Membrane-bound
Cytoplasmic
Secreted
Other/ungrouped
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