TNFRSF18
From Wikipedia, the free encyclopedia
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Tumor necrosis factor receptor superfamily, member 18
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| Identifiers | ||||||||||||||
| Symbol(s) | TNFRSF18; AITR; GITR; GITR-D | |||||||||||||
| External IDs | OMIM: 603905 MGI: 894675 HomoloGene: 48270 | |||||||||||||
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| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 8784 | 21936 | ||||||||||||
| Ensembl | ENSG00000186891 | ENSMUSG00000041954 | ||||||||||||
| Uniprot | Q9Y5U5 | Q540M6 | ||||||||||||
| Refseq | NM_004195 (mRNA) NP_004186 (protein) |
NM_009400 (mRNA) NP_033426 (protein) |
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| Location | Chr 1: 1.13 - 1.13 Mb | Chr 4: 154.87 - 154.87 Mb | ||||||||||||
| Pubmed search | [1] | [2] | ||||||||||||
Tumor necrosis factor receptor superfamily, member 18, also known as TNFRSF18, is a human gene.[1]
The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor has been shown to have increased expression upon T-cell activation, and it is thought to play a key role in dominant immunological self-tolerance maintained by CD25(+)CD4(+) regulatory T cells. Knockout studies in mice also suggest the role of this receptor is in the regulation of CD3-driven T-cell activation and programmed cell death. Three alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported.[1]
[edit] References
[edit] Further reading
- Nocentini G, Giunchi L, Ronchetti S, et al. (1997). "A new member of the tumor necrosis factor/nerve growth factor receptor family inhibits T cell receptor-induced apoptosis.". Proc. Natl. Acad. Sci. U.S.A. 94 (12): 6216–21. PMID 9177197.
- Kwon B, Yu KY, Ni J, et al. (1999). "Identification of a novel activation-inducible protein of the tumor necrosis factor receptor superfamily and its ligand.". J. Biol. Chem. 274 (10): 6056–61. PMID 10037686.
- Gurney AL, Marsters SA, Huang RM, et al. (1999). "Identification of a new member of the tumor necrosis factor family and its receptor, a human ortholog of mouse GITR.". Curr. Biol. 9 (4): 215–8. PMID 10074428.
- Nocentini G, Ronchetti S, Bartoli A, et al. (2000). "Identification of three novel mRNA splice variants of GITR.". Cell Death Differ. 7 (4): 408–10. doi:. PMID 10836847.
- Shimizu J, Yamazaki S, Takahashi T, et al. (2002). "Stimulation of CD25(+)CD4(+) regulatory T cells through GITR breaks immunological self-tolerance.". Nat. Immunol. 3 (2): 135–42. doi:. PMID 11812990.
- McHugh RS, Whitters MJ, Piccirillo CA, et al. (2002). "CD4(+)CD25(+) immunoregulatory T cells: gene expression analysis reveals a functional role for the glucocorticoid-induced TNF receptor.". Immunity 16 (2): 311–23. PMID 11869690.
- Ronchetti S, Nocentini G, Riccardi C, Pandolfi PP (2002). "Role of GITR in activation response of T lymphocytes.". Blood 100 (1): 350–2. doi:. PMID 12070049.
- Clark HF, Gurney AL, Abaya E, et al. (2003). "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment.". Genome Res. 13 (10): 2265–70. doi:. PMID 12975309.
- Zhang Z, Henzel WJ (2005). "Signal peptide prediction based on analysis of experimentally verified cleavage sites.". Protein Sci. 13 (10): 2819–24. doi:. PMID 15340161.
- Esparza EM, Arch RH (2005). "Glucocorticoid-induced TNF receptor, a costimulatory receptor on naive and activated T cells, uses TNF receptor-associated factor 2 in a novel fashion as an inhibitor of NF-kappa B activation.". J. Immunol. 174 (12): 7875–82. PMID 15944293.
- Baumgartner-Nielsen J, Vestergaard C, Thestrup-Pedersen K, et al. (2006). "Glucocorticoid-induced tumour necrosis factor receptor (GITR) and its ligand (GITRL) in atopic dermatitis.". Acta Derm. Venereol. 86 (5): 393–8. doi:. PMID 16955181.
- Baltz KM, Krusch M, Bringmann A, et al. (2007). "Cancer immunoediting by GITR (glucocorticoid-induced TNF-related protein) ligand in humans: NK cell/tumor cell interactions.". FASEB J. 21 (10): 2442–54. doi:. PMID 17360848.
- Lahey TP, Loisel SD, Wieland-Alter W (2007). "Glucocorticoid-induced tumor necrosis factor receptor family-related protein triggering enhances HIV-specific CD4+ T cell cytokine secretion and protects HIV-specific CD4+ T cells from apoptosis.". J. Infect. Dis. 196 (1): 43–9. doi:. PMID 17538882.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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