Lymphocyte antigen 96
From Wikipedia, the free encyclopedia
Lymphocyte antigen 96 is a protein that in humans is encoded by the LY96 gene.[1][2][3]
The protein encoded by this gene is involved in binding lipopolysaccharide with TLR 4. It is also known as "MD2".
The MD-2 protein appears to associate with toll-like receptor 4 on the cell surface and confers responsiveness to lipopolysaccaride (LPS), thus providing a link between the receptor and LPS signaling.[3]
Interactions
Lymphocyte antigen 96 has been shown to interact with TLR 4.[1][4]
References
- ↑ 1.0 1.1 Shimazu R, Akashi S, Ogata H, Nagai Y, Fukudome K, Miyake K, Kimoto M (Jul 1999). "MD-2, a Molecule that Confers Lipopolysaccharide Responsiveness on Toll-like Receptor 4". J Exp Med 189 (11): 1777–82. doi:10.1084/jem.189.11.1777. PMC 2193086. PMID 10359581.
- ↑ Abreu MT, Vora P, Faure E, Thomas LS, Arnold ET, Arditi M (Jul 2001). "Decreased expression of Toll-like receptor-4 and MD-2 correlates with intestinal epithelial cell protection against dysregulated proinflammatory gene expression in response to bacterial lipopolysaccharide". J Immunol 167 (3): 1609–16. PMID 11466383.
- ↑ 3.0 3.1 "Entrez Gene: LY96 lymphocyte antigen 96".
- ↑ Re, Fabio; Strominger Jack L (Jun 2002). "Monomeric recombinant MD-2 binds toll-like receptor 4 tightly and confers lipopolysaccharide responsiveness". J. Biol. Chem. (United States) 277 (26): 23427–32. doi:10.1074/jbc.M202554200. ISSN 0021-9258. PMID 11976338.
Further reading
- Kato K, Morrison AM, Nakano T et al. (2000). "ESOP-1, a secreted protein expressed in the hematopoietic, nervous, and reproductive systems of embryonic and adult mice". Blood 96 (1): 362–4. PMID 10891475.
- Dziarski R, Wang Q, Miyake K et al. (2001). "MD-2 enables Toll-like receptor 2 (TLR2)-mediated responses to lipopolysaccharide and enhances TLR2-mediated responses to Gram-positive and Gram-negative bacteria and their cell wall components". J. Immunol. 166 (3): 1938–44. PMID 11160242.
- Schromm AB, Lien E, Henneke P et al. (2001). "Molecular Genetic Analysis of an Endotoxin Nonresponder Mutant Cell Line: A Point Mutation in a Conserved Region of Md-2 Abolishes Endotoxin-Induced Signaling". J. Exp. Med. 194 (1): 79–88. doi:10.1084/jem.194.1.79. PMC 2193443. PMID 11435474.
- Visintin A, Mazzoni A, Spitzer JA, Segal DM (2001). "Secreted MD-2 is a large polymeric protein that efficiently confers lipopolysaccharide sensitivity to Toll-like receptor 4". Proc. Natl. Acad. Sci. U.S.A. 98 (21): 12156–61. doi:10.1073/pnas.211445098. PMC 59784. PMID 11593030.
- Akashi S, Nagai Y, Ogata H et al. (2002). "Human MD-2 confers on mouse Toll-like receptor 4 species-specific lipopolysaccharide recognition". Int. Immunol. 13 (12): 1595–9. doi:10.1093/intimm/13.12.1595. PMID 11717200.
- Abreu MT, Arnold ET, Thomas LS et al. (2002). "TLR4 and MD-2 expression is regulated by immune-mediated signals in human intestinal epithelial cells". J. Biol. Chem. 277 (23): 20431–7. doi:10.1074/jbc.M110333200. PMID 11923281.
- Re F, Strominger JL (2002). "Monomeric recombinant MD-2 binds toll-like receptor 4 tightly and confers lipopolysaccharide responsiveness". J. Biol. Chem. 277 (26): 23427–32. doi:10.1074/jbc.M202554200. PMID 11976338.
- Latz E, Visintin A, Lien E et al. (2003). "Lipopolysaccharide rapidly traffics to and from the Golgi apparatus with the toll-like receptor 4-MD-2-CD14 complex in a process that is distinct from the initiation of signal transduction". J. Biol. Chem. 277 (49): 47834–43. doi:10.1074/jbc.M207873200. PMID 12324469.
- Strausberg RL, Feingold EA, Grouse LH et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Schröder NW, Morath S, Alexander C et al. (2003). "Lipoteichoic acid (LTA) of Streptococcus pneumoniae and Staphylococcus aureus activates immune cells via Toll-like receptor (TLR)-2, lipopolysaccharide-binding protein (LBP), and CD14, whereas TLR-4 and MD-2 are not involved". J. Biol. Chem. 278 (18): 15587–94. doi:10.1074/jbc.M212829200. PMID 12594207.
- Mullen GE, Kennedy MN, Visintin A et al. (2003). "The role of disulfide bonds in the assembly and function of MD-2". Proc. Natl. Acad. Sci. U.S.A. 100 (7): 3919–24. doi:10.1073/pnas.0630495100. PMC 153023. PMID 12642668.
- Ohnishi T, Muroi M, Tanamoto K (2004). "MD-2 Is Necessary for the Toll-Like Receptor 4 Protein To Undergo Glycosylation Essential for Its Translocation to the Cell Surface". Clin. Diagn. Lab. Immunol. 10 (3): 405–10. PMC 154975. PMID 12738639.
- Thompson PA, Tobias PS, Viriyakosol S et al. (2003). "Lipopolysaccharide (LPS)-binding protein inhibits responses to cell-bound LPS". J. Biol. Chem. 278 (31): 28367–71. doi:10.1074/jbc.M302921200. PMID 12754215.
- Visintin A, Latz E, Monks BG et al. (2004). "Lysines 128 and 132 enable lipopolysaccharide binding to MD-2, leading to Toll-like receptor-4 aggregation and signal transduction". J. Biol. Chem. 278 (48): 48313–20. doi:10.1074/jbc.M306802200. PMID 12960171.
- Re F, Strominger JL (2004). "Separate functional domains of human MD-2 mediate Toll-like receptor 4-binding and lipopolysaccharide responsiveness". J. Immunol. 171 (10): 5272–6. PMID 14607928.
- Hamann L, Kumpf O, Müller M et al. (2005). "A coding mutation within the first exon of the human MD-2 gene results in decreased lipopolysaccharide-induced signaling". Genes Immun. 5 (4): 283–8. doi:10.1038/sj.gene.6364068. PMID 15057266.
- Gruber A, Mancek M, Wagner H et al. (2004). "Structural model of MD-2 and functional role of its basic amino acid clusters involved in cellular lipopolysaccharide recognition". J. Biol. Chem. 279 (27): 28475–82. doi:10.1074/jbc.M400993200. PMID 15111623.
- Jia HP, Kline JN, Penisten A et al. (2004). "Endotoxin responsiveness of human airway epithelia is limited by low expression of MD-2". Am. J. Physiol. Lung Cell Mol. Physiol. 287 (2): L428–37. doi:10.1152/ajplung.00377.2003. PMID 15121639.
External links
- lymphocyte antigen 96, human at the US National Library of Medicine Medical Subject Headings (MeSH)
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