CD155

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PVR
Poliovirus binding receptor 1DGI.png
Available structures
PDB Human UniProt search: PDBe RCSB
Identifiers
Aliases PVR, CD155, HVED, NECL5, Necl-5, PVS, TAGE4, poliovirus receptor
External IDs OMIM: 173850 HomoloGene: 9672 GeneCards: 5817
Genetically Related Diseases
Disease Name References
multiple sclerosis
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001135768
NM_001135769
NM_001135770
NM_006505

n/a

RefSeq (protein)

NP_001129240.1
NP_001129241.1
NP_001129242.2
NP_006496.4

n/a

Location (UCSC) Chr 19: 44.64 – 44.66 Mb n/a
PubMed search [2] n/a
Wikidata
View/Edit Human

CD155 (cluster of differentiation 155) also known as the poliovirus receptor is a protein that in humans is encoded by the PVR gene.[3][4]

Function[edit]

CD155 is a Type I transmembrane glycoprotein in the immunoglobulin superfamily.[5] Commonly known as Poliovirus Receptor (PVR) due to its involvement in the cellular poliovirus infection in primates, CD155's normal cellular function is in the establishment of intercellular adherens junctions between epithelial cells.[6] The role of CD155 in the immune system is unclear, though it may be involved in intestinal humoral immune responses.[6] Subsequent data has also suggested that CD155 may also be used to positively select MHC-independent T cells in the thymus.

The external domain mediates cell attachment to the extracellular matrix molecule vitronectin, while its intracellular domain interacts with the dynein light chain Tctex-1/DYNLT1. The gene is specific to the primate lineage, and serves as a cellular receptor for poliovirus in the first step of poliovirus replication.[3]

Structure[edit]

CD155 is a transmembrane protein with 3 extracellular immunoglobulin-like domains, D1-D3, where D1 is recognized by the virus.[7]

Low resolution structures of CD155 complexed with poliovirus have been obtained using electron microscopy[8] while a high resolution structures of the ectodomain D1 and D2 of CD155 were solved by x-ray crystallography.[7]

See also[edit]

  • Vincent Racaniello, Professor in the Department of Microbiology and Immunology at Columbia University’s College of Physicians and Surgeons responsible for initial identification of CD155 as the poliovirus receptor protein.

References[edit]

  1. ^ "chibi.ubc.ca/Gemma/phenotypes.html?phenotypeUrlId=DOID_2377&geneId=136714". 
  2. ^ "Human PubMed Reference:". 
  3. ^ a b "Entrez Gene: poliovirus receptor". 
  4. ^ Koike S, Horie H, Ise I, Okitsu A, Yoshida M, Iizuka N, Takeuchi K, Takegami T, Nomoto A (October 1990). "The poliovirus receptor protein is produced both as membrane-bound and secreted forms". EMBO J. 9 (10): 3217–24. PMC 552052free to read. PMID 2170108. 
  5. ^ Mendelsohn CL, Wimmer E, Racaniello VR (1989). "Cellular receptor for poliovirus: molecular cloning, nucleotide sequence, and expression of a new member of the immunoglobulin superfamily". Cell. 56 (5): 855–65. doi:10.1016/0092-8674(89)90690-9. PMID 2538245. 
  6. ^ a b Maier MK, Seth S, Czeloth N, et al. (2007). "The adhesion receptor CD155 determines the magnitude of humoral immune responses against orally ingested antigens". European Journal of Immunology. 37 (8): 2214–25. doi:10.1002/eji.200737072. PMID 17621371. 
  7. ^ a b PDB: 3epc​, 3epd​, 3epf​, 3eow​; Zhang P, Mueller S, Morais MC, Bator CM, Bowman VD, Hafenstein S, Wimmer E, Rossmann MG (November 2008). "Crystal structure of CD155 and electron microscopic studies of its complexes with polioviruses". Proc. Natl. Acad. Sci. U.S.A. 105 (47): 18284–9. doi:10.1073/pnas.0807848105. PMC 2587566free to read. PMID 19011098. 
  8. ^ PDB: 1DGI​; He Y, Bowman VD, Mueller S, Bator CM, Bella J, Peng X, Baker TS, Wimmer E, Kuhn RJ, Rossmann MG (January 2000). "Interaction of the poliovirus receptor with poliovirus". Proc. Natl. Acad. Sci. U.S.A. 97 (1): 79–84. doi:10.1073/pnas.97.1.79. PMC 26619free to read. PMID 10618374. 

Further reading[edit]

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