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CD40 (protein): Wikis

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CD40 molecule, TNF receptor superfamily member 5
Identifiers
Symbols CD40; Bp50; CDW40; MGC9013; TNFRSF5; p50
External IDs OMIM109535 MGI88336 HomoloGene954 GeneCards: CD40 Gene
RNA expression pattern
PBB GE CD40 35150 at tn.png
PBB GE CD40 205153 s at tn.png
PBB GE CD40 215346 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 958 21939
Ensembl ENSG00000101017 ENSMUSG00000017652
UniProt P25942 Q3TS33
RefSeq (mRNA) NM_001250 NM_011611
RefSeq (protein) NP_001241 NP_035741
Location (UCSC) Chr 20:
44.18 - 44.37 Mb
Chr 2:
164.75 - 164.76 Mb
PubMed search [1] [2]

CD40 is a costimulatory protein found on antigen presenting cells and is required for their activation. The binding of CD154 (CD40L) on TH cells to CD40 activates antigen presenting cells and induces a variety of downstream effects.

The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor has been found to be essential in mediating a broad variety of immune and inflammatory responses including T cell-dependent immunoglobulin class switching, memory B cell development, and germinal center formation. AT-hook transcription factor AKNA is reported to coordinately regulate the expression of this receptor and its ligand, which may be important for homotypic cell interactions. Adaptor protein TNFR2 interacts with this receptor and serves as a mediator of the signal transduction. The interaction of this receptor and its ligand is found to be necessary for amyloid-beta-induced microglial activation, and thus is thought to be an early event in Alzheimer disease pathogenesis. Two alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported.[1]

Contents

Specific effects on cells

In the macrophage, the primary signal for activation is IFN-γ from Th1 type CD4 T cells. The secondary signal is CD40L on the T cell which binds CD40 on the macrophage cell surface. As a result, the macrophage expresses more CD40 and TNF receptors on its surface which helps increase the level of activation. The increase in activation results in the induction of potent microbicidal substances in the macrophage, including reactive oxygen species and nitric oxide, leading to the destruction of ingested microbe.

The B cell can present antigens to helper T cells. If the T cell recognizes the peptide presented by the B cell, the T cell synthesizes CD40L. The CD40L binds to the B cell's CD40 receptor which causes resting B cell activation. The T cell also produces IL-4 which directly binds to B cell receptors. As a result of this interaction, the B cell can undergo division, antibody isotype switching, and differentiation to plasma cells. The end result is a B cell which is able to mass produce specific antibodies against an antigenic target.

Interactions

CD40 (protein) has been shown to interact with TRAF2,[2][3][4] TRAF3,[3][5][6][7] TRAF6,[3][7] TRAF5[3][8] and TTRAP.[9]

References

  1. ^ "Entrez Gene: CD40 CD40 molecule, TNF receptor superfamily member 5". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=958.  
  2. ^ McWhirter, S M; Pullen S S, Holton J M, Crute J J, Kehry M R, Alber T (Jul. 1999). "Crystallographic analysis of CD40 recognition and signaling by human TRAF2". Proc. Natl. Acad. Sci. U.S.A. (UNITED STATES) 96 (15): 8408–13. ISSN 0027-8424. PMID 10411888.  
  3. ^ a b c d Tsukamoto, N; Kobayashi N, Azuma S, Yamamoto T, Inoue J (Feb. 1999). "Two differently regulated nuclear factor kappaB activation pathways triggered by the cytoplasmic tail of CD40". Proc. Natl. Acad. Sci. U.S.A. (UNITED STATES) 96 (4): 1234–9. ISSN 0027-8424. PMID 9990007.  
  4. ^ Malinin, N L; Boldin M P, Kovalenko A V, Wallach D (Feb. 1997). "MAP3K-related kinase involved in NF-kappaB induction by TNF, CD95 and IL-1". Nature (ENGLAND) 385 (6616): 540–4. doi:10.1038/385540a0. ISSN 0028-0836. PMID 9020361.  
  5. ^ Hu, H M; O'Rourke K, Boguski M S, Dixit V M (Dec. 1994). "A novel RING finger protein interacts with the cytoplasmic domain of CD40". J. Biol. Chem. (UNITED STATES) 269 (48): 30069–72. ISSN 0021-9258. PMID 7527023.  
  6. ^ Ni, C Z; Welsh K, Leo E, Chiou C K, Wu H, Reed J C, Ely K R (Sep. 2000). "Molecular basis for CD40 signaling mediated by TRAF3". Proc. Natl. Acad. Sci. U.S.A. (UNITED STATES) 97 (19): 10395–9. ISSN 0027-8424. PMID 10984535.  
  7. ^ a b Roy, N; Deveraux Q L, Takahashi R, Salvesen G S, Reed J C (Dec. 1997). "The c-IAP-1 and c-IAP-2 proteins are direct inhibitors of specific caspases". EMBO J. (ENGLAND) 16 (23): 6914–25. doi:10.1093/emboj/16.23.6914. ISSN 0261-4189. PMID 9384571.  
  8. ^ Ishida, T K; Tojo T, Aoki T, Kobayashi N, Ohishi T, Watanabe T, Yamamoto T, Inoue J (Sep. 1996). "TRAF5, a novel tumor necrosis factor receptor-associated factor family protein, mediates CD40 signaling". Proc. Natl. Acad. Sci. U.S.A. (UNITED STATES) 93 (18): 9437–42. ISSN 0027-8424. PMID 8790348.  
  9. ^ Pype, S; Declercq W, Ibrahimi A, Michiels C, Van Rietschoten J G, Dewulf N, de Boer M, Vandenabeele P, Huylebroeck D, Remacle J E (Jun. 2000). "TTRAP, a novel protein that associates with CD40, tumor necrosis factor (TNF) receptor-75 and TNF receptor-associated factors (TRAFs), and that inhibits nuclear factor-kappa B activation". J. Biol. Chem. (UNITED STATES) 275 (24): 18586–93. doi:10.1074/jbc.M000531200. ISSN 0021-9258. PMID 10764746.  

Further reading

  • Parham, Peter (2004). The Immune System (2nd ed.). Garland Science. pp. 169–173. ISBN 0-8153-4093-1.  
  • Coico R, Sunshine G, and Benjamin E (2003). Immunology: A Short Course. p. 97.  
  • Clark EA (1991). "CD40: a cytokine receptor in search of a ligand.". Tissue Antigens 36 (1): 33–6. doi:10.1111/j.1399-0039.1990.tb01795.x. PMID 1701063.  
  • Banchereau J, Bazan F, Blanchard D, et al. (1994). "The CD40 antigen and its ligand.". Annu. Rev. Immunol. 12: 881–922. doi:10.1146/annurev.iy.12.040194.004313. PMID 7516669.  
  • van Kooten C, Banchereau J (2000). "CD40-CD40 ligand.". J. Leukoc. Biol. 67 (1): 2–17. PMID 10647992.  
  • Schattner EJ (2003). "CD40 ligand in CLL pathogenesis and therapy.". Leuk. Lymphoma 37 (5-6): 461–72. PMID 11042507.  
  • Bhushan A, Covey LR (2002). "CD40:CD40L interactions in X-linked and non-X-linked hyper-IgM syndromes.". Immunol. Res. 24 (3): 311–24. doi:10.1385/IR:24:3:311. PMID 11817328.  
  • Cheng G, Schoenberger SP (2002). "CD40 signaling and autoimmunity.". Curr. Dir. Autoimmun. 5: 51–61. doi:10.1159/000060547. PMID 11826760.  
  • Dallman C, Johnson PW, Packham G (2003). "Differential regulation of cell survival by CD40.". Apoptosis 8 (1): 45–53. doi:10.1023/A:1021696902187. PMID 12510151.  
  • O'Sullivan B, Thomas R (2004). "Recent advances on the role of CD40 and dendritic cells in immunity and tolerance.". Curr. Opin. Hematol. 10 (4): 272–8. doi:10.1097/00062752-200307000-00004. PMID 12799532.  
  • Benveniste EN, Nguyen VT, Wesemann DR (2004). "Molecular regulation of CD40 gene expression in macrophages and microglia.". Brain Behav. Immun. 18 (1): 7–12. doi:10.1016/j.bbi.2003.09.001. PMID 14651941.  
  • Xu Y, Song G (2005). "The role of CD40-CD154 interaction in cell immunoregulation.". J. Biomed. Sci. 11 (4): 426–38. doi:10.1159/000077892. PMID 15153777.  
  • Contin C, Couzi L, Moreau JF, et al. (2004). "[Immune dysfuntion of uremic patients: potential role for the soluble form of CD40]". Néphrologie 25 (4): 119–26. PMID 15291139.  
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