Ku80 autoantigen as a cellular coreceptor for human parvovirus B19 infection

Yasuhiko Munakata, Takako Saito-Ito, Keiko Kumura-Ishii, Jie Huang, Takao Kodera, Tomonori Ishii, Yasuhiko Hirabayashi, Yoshio Koyanagi, Takeshi Sasaki

Research output: Contribution to journalArticlepeer-review

133 Citations (Scopus)

Abstract

Human parvovirus B19 (B19) infects human erythroid cells expressing P antigen. However, some cell lines that were positive for P antigen failed to bind B19, whereas some cell lines had an ability to bind B19 despite undetectable expression of P antigen. We here demonstrate that B19 specifically binds with Ku80 autoantigen on the cell surface. Furthermore, transfection of HeLa cells with the gene of Ku80 enabled the binding of B19 and allowed its entry into cells. Moreover, reduction of cell-surface expression of Ku80 in KU812Ep6 cells, which was a high-sensitive cell line for B19 infection, by short interfering RNA for Ku80 resulted in the marked inhibition of B19 binding in KU812Ep6 cells. Although Ku80 originally has been described as a nuclear protein, human bone marrow erythroid cells with glycophorin A or CD36, B cells with CD20, or T cells with CD3 were all positive for cell-surface expression of Ku80. B19 infection of KU812Ep6 cells and bone marrow cells was inhibited in the presence of anti-Ku80 antibody. Our data suggest that Ku80 functions as a novel coreceptor for B19 infection, and this finding may provide an explanation for the pathologic immunity associated with B19 infection.

Original languageEnglish
Pages (from-to)3449-3456
Number of pages8
JournalBlood
Volume106
Issue number10
DOIs
Publication statusPublished - 2005 Nov 15

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

Fingerprint Dive into the research topics of 'Ku80 autoantigen as a cellular coreceptor for human parvovirus B19 infection'. Together they form a unique fingerprint.

Cite this