Human P-selectin glycoprotein ligand-1 is a functional receptor for enterovirus 71

Nature Medicine

Volumn 15, Issue 7, 2009, Pages 794-797

  Nishimura, Yorihiro ^a   Shimojima, Masayuki ^b   Tano, Yoshio ^a,c   Miyamura, Tatsuo ^a   Wakita, Takaji ^a   Shimizu, Hiroyuki ^a  

^a NATIONAL INSTITUTE OF INFECTIOUS DISEASES   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

^c Japan Poliomyelitis Research Institute   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; P SELECTIN GLYCOPROTEIN LIGAND 1; VIRUS RECEPTOR;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; CHILD; CONTROLLED STUDY; CYTOPATHOGENIC EFFECT; ENTEROVIRUS 71; HAND FOOT AND MOUTH DISEASE; HUMAN; HUMAN CELL; LEUKEMIA CELL LINE; LEUKOCYTE; MOUSE; NONHUMAN; PATHOGENESIS; PLANT GROWTH; PRIORITY JOURNAL; PROTEIN EXPRESSION; T LYMPHOCYTE; VIRUS ENTRY; VIRUS REPLICATION; VIRUS STRAIN;

ANIMALS; CELL LINE; ENTEROVIRUS A, HUMAN; HUMANS; JURKAT CELLS; MEMBRANE GLYCOPROTEINS; MICE; RECEPTORS, VIRUS; VIRUS REPLICATION;

ENTEROVIRUS; HUMAN ENTEROVIRUS 71;

EID: 67650491431     PISSN: 10788956     EISSN: 1546170X     Source Type: Journal    
DOI: 10.1038/nm.1961     Document Type: Article

References (29)

1. Rossmann, M.G., He, Y. & Kuhn, R.J. Picornavirus-receptor interactions. Trends Microbiol. 10, 324-331 (2002).
2. Laszik, Z. et al. P-selectin glycoprotein ligand-1 is broadly expressed in cells of myeloid, lymphoid, and dendritic lineage and in some nonhematopoietic cells. Blood 88, 3010-3021 (1996).
3. Sako, D. et al. Expression cloning of a functional glycoprotein ligand for P-selectin. Cell 75, 1179-1186 (1993).
4. x and PSGL-1. Cell 103, 467-479 (2000).
5. Shimojima, M. et al. Usage of myeloma and panning in retrovirus-mediated expression cloning. Anal. Biochem. 315, 138-140 (2003).
6. Oberste, M.S., Maher, K., Kilpatrick, D.R. & Pallansch, M.A. Molecular evolution of the human enteroviruses: correlation of serotype with VP1 sequence and application to picornavirus classification. J. Virol. 73, 1941-1948 (1999).
7. Chan, L.G. et al. Deaths of children during an outbreak of hand, foot and mouth disease in Sarawak, Malaysia: clinical and pathological characteristics of the disease. Clin. Infect. Dis. 31, 678-683 (2000).
8. Ho, M. et al. An epidemic of enterovirus 71 infection in Taiwan. N. Engl. J. Med. 341, 929-935 (1999).
9. McMinn, P.C. An overview of the evolution of enterovirus 71 and its clinical and public health significance. FEMS Microbiol. Rev. 26, 91-107 (2002).
10. Lin, T.Y., Hsia, S.H., Huang, Y.C., Wu, C.T. & Chang, L.Y Proinflammatory cytokine reactions in enterovirus 71 infections of the central nervous system. Clin. Infect. Dis. 36, 269-274 (2003).
11. Wang, S.M. et al. Pathogenesis of enterovirus 71 brainstem encephalitis in pediatric patients: roles of cytokines and cellular immune activation in patients with pulmonary edema. J. Infect. Dis. 188, 564-570 (2003).
12. Chen, L.C. et al. Enterovirus 71 infection induces Fas ligand expression and apoptosis of Jurkat cells. J. Med. Virol. 78, 780-786 (2006).
13. Snapp, K.R. et al. A novel P-selectin glycoprotein ligand-1 monoclonal antibody recognizes an epitope within the tyrosine sulfate motif of human PSGL-1 and blocks recognition of both P- and L-selectin. Blood 91, 154-164 (1998).
14. Thatte, A. et al. Binding of function-blocking mAbs to mouse and human P-selectin glycoprotein ligand-1 peptides with and without tyrosine sulfation. J. Leukoc. Biol. 72, 470-477 (2002).
15. Li, F. et al. Visualization of P-selectin glycoprotein ligand-1 as a highly extended molecule and mapping of protein epitopes for monoclonal antibodies. J. Biol. Chem. 271, 6342-6348 (1996).
16. Brown, B.A., Oberste, M.S., Alexander, J.P. Jr., Kennett, M.L. & Pallansch, M.A. Molecular epidemiology and evolution of enterovirus 71 strains isolated from 1970 to 1998. J. Virol. 73, 9969-9975 (1999).
17. Arita, M., Ami, Y., Wakita, T. & Shimizu, H. Cooperative effect of the attenuation determinants derived from poliovirus Sabin 1 strain is essential for attenuation of enterovirus 71 in the NOD/SClD mouse infection model. J. Virol. 82, 1787-1797 (2008).
18. Chua, B.H., Phuektes, P., Sanders, S.A., Nicholls, P.K. & McMinn, PC. The molecular basis of mouse adaptation by human enterovirus 71. J. Gen. Virol. 89, 1622-1632 (2008).
19. Kung, CM. et al. Differences in replication capacity between enterovirus 71 isolates obtained from patients with encephalitis and those obtained from patients with herpangina in Taiwan. J. Med. Virol. 79, 60-68 (2007).
20. Kuo, R.L., Kung, S.H., Hsu, YY & Liu, W.T. Infection with enterovirus 71 or expression of its 2A protease induces apoptotic cell death. J. Gen. Virol. 83, 1367-1376 (2002).
21. Hsueh, C. et al. Acute encephalomyelitis during an outbreak of enterovirus type 71 infection in Taiwan: report of an autopsy case with pathologic, immunofluorescence and molecular studies. Mod. Pathol. 13, 1200-1205 (2000).
22. Wong, K.T. et al. The distribution of inflammation and virus in human enterovirus 71 encephalomyelitis suggests possible viral spread by neural pathways. J. Neuropathol. Exp. Neurol. 67, 162-169 (2008).
23. Nagata, N. et al. Pyramidal and extrapyramidal involvement in experimental infection of cynomolgus monkeys with enterovirus 71. J. Med. Virol. 67, 207-216 (2002).
24. Nagata, N. et al. Differential localization of neurons susceptible to enterovirus 71 and poliovirus type 1 in the central nervous system of cynomolgus monkeys after intravenous inoculation. J. Gen. Virol. 85, 2981-2989 (2004).
25. Ong, K.C. et al. Pathologic characterization of a murine model of human enterovirus 71 encephalomyelitis. J. Neuropathol. Exp. Neurol. 67, 532-542 (2008).
26. Chang, S.C., Lin, J.Y., Lo, L.Y.C., Li, M.L. & Shih, S.R. Diverse apoptotic pathways in enterovirus 71-infected cells. J. Neurovirol. 10, 338-349 (2004).
27. Chen, C.S. et al. Retrograde axonal transport: a major transmission route of enterovirus 71 in mice. J. Virol. 81, 8996-9003 (2007).
28. World Health Organization. Outbreak news. Enterovirus, China. Wkly. Epidemiol. Rec. 83, 169-170 (2008).
29. Kitamura, T. & Morikawa, Y. Isolation of T-cell antigens by retrovirus-mediated expression cloning. Methods Mol. Biol. 134, 143-152 (2000).