EPSTEIN-BARR-VIRUS COMPLEMENT C3D RECEPTOR IS AN INTERFERON-ALPHA RECEPTOR

被引:111
作者
DELCAYRE, AX
SALAS, F
MATHUR, S
KOVATS, K
LOTZ, M
LERNHARDT, W
机构
[1] CALIF INST BIOL RES, 11099 N TORREY PINES RD, LA JOLLA, CA 92037 USA
[2] UNIV CALIF SAN DIEGO, DEPT MED, LA JOLLA, CA 92093 USA
关键词
LYMPHOCYTES; EBV; C3D RECEPTOR; INTERFERON-ALPHA RECEPTOR; RECEPTOR BINDING MOTIF;
D O I
10.1002/j.1460-2075.1991.tb08025.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interferon-alpha contains a sequence motif similar to the complement receptor type two (CR2/CD21) binding site on complement fragment C3d. Antibodies against a peptide with the CR2 binding sequence on C3d react with a peptide carrying the IFN-alpha CR2 binding motif (residues 92-99) and with recombinant IFN-alpha. The IFN-alpha-derived peptide, as well as recombinant IFN-alpha, inhibits C3bi/C3d interaction with CR2 on the Burkitt lymphoma Raji. The direct interaction of IFN-alpha and CR2 is inhibited by polyclonal anti-IFN-alpha, anti-CR2 and anti-C3d peptide antibodies as well as by C3bi/C3d, EBV coat protein gp350/220 and IFN but not by IFN-gamma. [I-125]IFN-alpha binding to Raji cells is inhibited by polyclonal anti-IFN-alpha and anti-CR2 antibodies, by peptides with the CR2 binding motif and partially by C3bi/C3d. Monoclonal anti-CR2 antibody HB5, but not OKB-7, blocks IFN-alpha binding to Raji cells. CR2 or CR2-like molecules may therefore be the major IFN-alpha receptors on B lymphocytes.
引用
收藏
页码:919 / 926
页数:8
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