Complement component 3

C3
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 4ONT, 1C3D, 1GHQ, 1W2S, 2A73, 2A74, 2GOX, 2I07, 2ICE, 2ICF, 2NOJ, 2QKI, 2WII, 2WIN, 2WY7, 2WY8, 2XQW, 2XWB, 2XWJ, 3D5R, 3D5S, 3G6J, 3L3O, 3L5N, 3NMS, 3OED, 3OHX, 3OXU, 3RJ3, 3T4A, 4HW5, 4HWJ, 4I6O, 4M76, 4ZH1, 5FOB, 5FO9, 5FO7, 5FO8, 5FOA
Identifiers
Aliases	C3, AHUS5, ARMD9, ASP, C3a, C3b, CPAMD1, HEL-S-62p, complement component 3, complement C3
External IDs	OMIM: 120700 MGI: 88227 HomoloGene: 68031 GeneCards: C3
Gene location (Human) Chr. Chromosome 19 (human)[1] Band 19p13.3 Start 6,677,704 bp[1] End 6,730,562 bp[1]
Gene location (Mouse) Chr. Chromosome 17 (mouse)[2] Band 17 D|17 29.72 cM Start 57,203,970 bp[2] End 57,228,136 bp[2]
Gene ontology Molecular function • C5L2 anaphylatoxin chemotactic receptor binding • protein binding • endopeptidase inhibitor activity • receptor binding • serine-type endopeptidase activity Cellular component • blood microparticle • plasma membrane • extracellular fluid • extracellular region • extracellular exosome Biological process • G-protein coupled receptor signaling pathway • positive regulation of phagocytosis • positive regulation of protein phosphorylation • Alternative complement pathway • Lipid metabolism • immune system process • complement activation • positive regulation of lipid storage • positive regulation of type IIa hypersensitivity • fatty acid metabolic process • positive regulation of angiogenesis • positive regulation of G-protein coupled receptor protein signaling pathway • positive regulation of apoptotic cell clearance • immune response • Classical complement pathway • regulation of immune response • positive regulation of activation of membrane attack complex • positive regulation of vascular endothelial growth factor production • inflammatory response • positive regulation of glucose transport • regulation of complement activation • signal transduction • negative regulation of endopeptidase activity • regulation of triglyceride biosynthetic process • proteolysis • innate immune response Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	718	12266
Ensembl	ENSG00000125730	ENSMUSG00000024164
UniProt	P01024	P01027
RefSeq (mRNA)	NM_000064	NM_009778
RefSeq (protein)	NP_000055	NP_033908
Location (UCSC)	Chr 19: 6.68 – 6.73 Mb	Chr 17: 57.2 – 57.23 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

Complement component 3, often simply called C3, is a protein of the immune system. It plays a central role in the complement system and contributes to innate immunity. In humans it is encoded on chromosome 19 by a gene called C3.^[5][6]

Contents

• 
  1 Function
  


• 
  2 Structure
  


• 
  3 Biochemistry
  
  
  
  • 
    3.1 Biosynthesis
    
  
  
  
  


• 
  4 Clinical use
  


• 
  5 Interactions
  


• 
  6 Pathology
  


• 
  7 References
  


• 
  8 Further reading
  


• 
  9 External links
  

Function

C3 plays a central role in the activation of complement system.^[7] Its activation is required for both classical and alternative complement activation pathways. People with C3 deficiency are susceptible to bacterial infection.^[8][9]

One form of C3-convertase, also known as C4b2b, is formed by a heterodimer of activated forms of C4 and C2. It catalyzes the proteolytic cleavage of C3 into C3a and C3b, generated during activation through the classical pathway as well as the lectin pathway. C3a is an anaphylotoxin and the precursor of some cytokines such as ASP, and C3b serves as an opsonizing agent. Factor I can cleave C3b into C3c and C3d, the latter of which plays a role in enhancing B cell responses. In the alternative complement pathway, C3 is cleaved by C3bBb, another form of C3-convertase composed of activated forms of C3 (C3b) and factor B (Bb). Once C3 is activated to C3b, it exposes a reactive thioester that allows the peptide to covalently attach to any surface that can provide a nucleophile such as a primary amine or a hydroxyl group. Activated C3 can then interact with factor B. Factor B is then activated by factor D, to form Bb. The resultant complex, C3bBb, is called the alternative pathway (AP) C3 convertase.

C3bBb is deactivated in steps. First, the proteolytic component of the convertase, Bb, is removed by complement regulatory proteins having decay-accelerating factor (DAF) activity. Next, C3b is broken down progressively to first iC3b, then C3c + C3dg, and then finally C3d. Factor I is the protease that performs these cuts but it requires the help of another protein (Factor H, CR1, MCP or C4BP) to supply cofactor activity.

Structure

Several crystallographic structures of C3 have been determined^[10] and reveal that this protein contains 13 domains.^{[11][12][13][14]}

Biochemistry

Biosynthesis

In humans, C3 is predominantly synthesised by liver hepatocytes^[5] and to some degree by epidermis keratinocytes.^[15]

Clinical use

Complement tests

C4 (C)	FB (A)	C3	CH50	Conditions
·	↓	↓	↓	PSG, C3 NeF AA
↓	·	↓	·	HAE, C4D
·	·	·	↓	TCPD
↓	· /↓	↓	↓	SLE
↑	↑	↑	↑	inflammation

Levels of C3 in the blood may be measured to support or refute a particular medical diagnosis. For example, low C3 levels are associated with Systemic Lupus Erythematosus (SLE)^[16]
and some types of kidney disease such as post-infectious glomerulonephritis, membranoproliferative glomerulonephritis, and shunt nephritis.

.

Interactions

Complement component 3 has been shown to interact with Factor H.^[17][18]

Pathology

Deficiencies in C3 lead to genetic infections, usually fatal to the newborn.^[19]

References

1. 
   ^ ^abc GRCh38: Ensembl release 89: ENSG00000125730 - Ensembl, May 2017
   


2. 
   ^ ^abc GRCm38: Ensembl release 89: ENSMUSG00000024164 - Ensembl, May 2017
   


3. 
   ^ "Human PubMed Reference:"..mw-parser-output cite.citation{font-style:inherit}.mw-parser-output q{quotes:"""""""'""'"}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-limited a,.mw-parser-output .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}
   


4. 
   ^ "Mouse PubMed Reference:".
   


5. 
   ^ ^ab de Bruijn MH, Fey GH (Feb 1985). "Human complement component C3: cDNA coding sequence and derived primary structure". Proceedings of the National Academy of Sciences of the United States of America. 82 (3): 708–12. doi:10.1073/pnas.82.3.708. PMC 397115. PMID 2579379.
   


6. 
   ^ "Entrez Gene: C3 complement component 3".
   


7. 
   ^ Sahu A, Lambris JD (Apr 2001). "Structure and biology of complement protein C3, a connecting link between innate and acquired immunity". Immunological Reviews. 180: 35–48. doi:10.1034/j.1600-065X.2001.1800103.x. PMID 11414361.
   


8. 
   ^ Lachmann P (Dec 1975). "Genetics of the complement system". Journal of Medical Genetics. 12 (4): 372–7. doi:10.1136/jmg.12.4.372. PMC 1013316. PMID 768477.
   


9. 
   ^ Matsuyama W, Nakagawa M, Takashima H, Muranaga F, Sano Y, Osame M (Dec 2001). "Molecular analysis of hereditary deficiency of the third component of complement (C3) in two sisters". Internal Medicine. 40 (12): 1254–8. doi:10.2169/internalmedicine.40.1254. PMID 11813855.
   


10. 
    ^ "Advanced search results for UniProt accession P01024". Protein Data Bank in Europe (PDBe). European Bioinformatics Institute. Retrieved 2010-12-27.
    


11. 
    ^ Janssen BJ, Huizinga EG, Raaijmakers HC, Roos A, Daha MR, Nilsson-Ekdahl K, Nilsson B, Gros P (Sep 2005). "Structures of complement component C3 provide insights into the function and evolution of immunity". Nature. 437 (7058): 505–11. doi:10.1038/nature04005. PMID 16177781.
    


12. 
    ^ Janssen BJ, Christodoulidou A, McCarthy A, Lambris JD, Gros P (Nov 2006). "Structure of C3b reveals conformational changes that underlie complement activity". Nature. 444 (7116): 213–6. doi:10.1038/nature05172. PMID 17051160.
    


13. 
    ^ Wiesmann C, Katschke KJ, Yin J, Helmy KY, Steffek M, Fairbrother WJ, McCallum SA, Embuscado L, DeForge L, Hass PE, van Lookeren Campagne M (Nov 2006). "Structure of C3b in complex with CRIg gives insights into regulation of complement activation". Nature. 444 (7116): 217–20. doi:10.1038/nature05263. PMID 17051150.
    


14. 
    ^ Fredslund F, Jenner L, Husted LB, Nyborg J, Andersen GR, Sottrup-Jensen L (Aug 2006). "The structure of bovine complement component 3 reveals the basis for thioester function". Journal of Molecular Biology. 361 (1): 115–27. doi:10.1016/j.jmb.2006.06.009. PMID 16831446.
    


15. 
    ^ Pasch, Marcel C.; van den Bosch, Norbert H.A.; Bos, Jan D.; Asghar, Syed S.; Daha, Mohamed R. (January 2000). "Synthesis of Complement Components C3 and Factor B in Human Keratinocytes is Differentially Regulated by Cytokines". Journal of Investigative Dermatology. 114 (1): 78-82. doi:10.1046/j.1523-1747.2000.00841.x. Retrieved 28 August 2017.
    


16. 
    ^ https://www.urmc.rochester.edu/encyclopedia/content.aspx?contenttypeid=167&contentid=complement_c3_blood
    


17. 
    ^ Soames CJ, Sim RB (Sep 1997). "Interactions between human complement components factor H, factor I and C3b". The Biochemical Journal. 326 (2): 553–61. doi:10.1042/bj3260553. PMC 1218704. PMID 9291131.
    


18. 
    ^ Jokiranta TS, Westin J, Nilsson UR, Nilsson B, Hellwage J, Löfås S, Gordon DL, Ekdahl KN, Meri S (Mar 2001). "Complement C3b interactions studied with surface plasmon resonance technique". International Immunopharmacology. 1 (3): 495–506. doi:10.1016/S1567-5769(00)00042-4. PMID 11367533.
    


19. 
    ^ Abbas, Abul K.; Lichtman, Andrew H.; Pillai, Shiv (2012). "Chapter 8: Effector Mechanisms of Humoral Immunity". Basic Immunology: Functions and Disorders of the Immune System (Fourth ed.). Philadelphia, PA: Elsevier Saunders. p. 162. ISBN 978-1-4557-0707-2.
    

Further reading

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• 
  Bradley DT, Zipfel PF, Hughes AE (Jun 2011). "Complement in age-related macular degeneration: a focus on function". Eye. 25 (6): 683–93. doi:10.1038/eye.2011.37. PMC 3178140. PMID 21394116.
  

External links

• GeneReviews/NCBI/NIH/UW entry on Atypical Hemolytic-Uremic Syndrome


• OMIM entries on Atypical Hemolytic-Uremic Syndrome


• GeneReviews/NCBI/NIH/UW entry on Dense Deposit Disease/Membranoproliferative Glomerulonephritis Type II


• 
  Complement+C3 at the US National Library of Medicine Medical Subject Headings (MeSH)

v t e complement system
Pathways	C L A
Activators/enzymes	Early C: C1 C1q C1r C1s C4 C4a C4b C2 L: MASP1/MASP2 MBL A: Factor B Factor D Factor P/Properdin Middle C3 C3a C3b/iC3b C5 C5a C5b C3-convertase C5-convertase Late MAC C5b C6 C7 C8 C9
Inhibitors	CLA: C1-inhibitor Decay-accelerating factor/CD59 Factor I CL: C4BP A: Factor H
Complement receptors	CR1 CR2 CR3 CR4 CD11b/CD11c/CD18 Anaphylatoxin C3a C5a
Function	Cytotoxicity(by MAC) immune adherence Inducing inflammation Opsonization

v t e Acute-phase proteins
Amyloid	SAP SAA
Other positive	Alpha 1-antichymotrypsin Alpha 1-antitrypsin Alpha 2-macroglobulin C-reactive protein Ceruloplasmin C3 Ferritin Fibrin Haptoglobin Hemopexin Orosomucoid
Negative	Serum albumin Transferrin

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

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