Nucleolin as the earliest target molecule of autoantibodies produced in MRL/lpr lupus-prone mice

被引:21
作者
Hirata, D [1 ]
Iwamoto, M [1 ]
Yoshio, T [1 ]
Okazaki, H [1 ]
Masuyama, J [1 ]
Mimori, A [1 ]
Minota, S [1 ]
机构
[1] Jichi Med Sch, Div Clin Immunol & Rheumatol, Minami Kawachi, Tochigi 3290498, Japan
关键词
rodent; lupus; autoimmunity; autoantibodies; nucleolin;
D O I
10.1006/clim.2000.4916
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To elucidate the autoantigen against which autoantibodies are produced in the earliest phase of the disease:process of systemic lupus erythematosus (SLE), serum samples were collected individually and serially from 10 NZB/NZW F1 and 10 MRL/lpr mice. Using immunoblots with mouse thymoma cell (EL-4) lysates as substrates, all mice were found to generate autoantibody against an either 150-kDa, 110-kDa, 75-kDa, or 55 kDa molecule in as early as 4 weeks. Anti-DNA antibodies occurred almost at the same time or after those against these four molecules. The number of antigens reactive with autoantibodies in immunoblots increased gradually with age. Antibodies against histone molecules were produced after 8 weeks of age. Among the four antigens, the 110-kDa molecule was identified as nucleolin, which is an abundant nucleolar phosphoprotein. Nucleolin binds DNA, RNA, and nucleic acid-binding proteins such as histone H1. Nucleolin is a target of granzyme A of cytotoxic T cells, and autoantibodies against it are found in sera from patients with SLE as well as from those with various viral infections. These results indicate that nucleolin is one of the immunodominant molecules that break down self-tolerance and initiate autoantibody-spreading in a mouse model of SLE. (C) 2000 Academic Press.
引用
收藏
页码:50 / 58
页数:9
相关论文
共 41 条
[1]  
Behar S M, 1989, Int Rev Immunol, V5, P23, DOI 10.3109/08830188909086988
[2]   MAJOR NUCLEOLAR PROTEINS SHUTTLE BETWEEN NUCLEUS AND CYTOPLASM [J].
BORER, RA ;
LEHNER, CF ;
EPPENBERGER, HM ;
NIGG, EA .
CELL, 1989, 56 (03) :379-390
[3]  
BUGLER B, 1987, J BIOL CHEM, V262, P10922
[4]   AUTOANTIGENS TARGETED IN SYSTEMIC LUPUS-ERYTHEMATOSUS ARE CLUSTERED IN 2 POPULATIONS OF SURFACE-STRUCTURES ON APOPTOTIC KERATINOCYTES [J].
CASCIOLAROSEN, LA ;
ANHALT, G ;
ROSEN, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (04) :1317-1330
[5]   DNA-DEPENDENT PROTEIN-KINASE IS ONE OF A SUBSET OF AUTOANTIGENS SPECIFICALLY CLEAVED EARLY DURING APOPTOSIS [J].
CASCIOLAROSEN, LA ;
ANHALT, GJ ;
ROSEN, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (06) :1625-1634
[6]   Selective cleavage of nuclear autoantigens during CD95 (Fas/APO-1)-mediated T cell apoptosis [J].
Casiano, CA ;
Martin, SJ ;
Green, DR ;
Tan, EM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (02) :765-770
[7]   INDUCTION OF A CATIONIC SHIFT IN IGG ANTI-DNA AUTOANTIBODIES - ROLE OF T-HELPER CELLS WITH CLASSICAL AND NOVEL PHENOTYPES IN 3 MURINE MODELS OF LUPUS NEPHRITIS [J].
DATTA, SK ;
PATEL, H ;
BERRY, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 165 (05) :1252-1268
[8]   NUCLEOLIN IS A MATRIX ATTACHMENT REGION DNA-BINDING PROTEIN THAT SPECIFICALLY RECOGNIZES A REGION WITH HIGH BASE-UNPAIRING POTENTIAL [J].
DICKINSON, LA ;
KOHWISHIGEMATSU, T .
MOLECULAR AND CELLULAR BIOLOGY, 1995, 15 (01) :456-465
[9]   RESTRICTED SUB-POPULATIONS OF DNA ANTIBODIES IN KIDNEYS OF MICE WITH SYSTEMIC LUPUS - COMPARISON OF ANTIBODIES IN SERUM AND RENAL ELUATES [J].
EBLING, F ;
HAHN, BH .
ARTHRITIS AND RHEUMATISM, 1980, 23 (04) :392-403
[10]   STOCHASTIC-CONTROL OF ANTI-SM AUTOANTIBODIES IN MRL/MP-LPR/LPR MICE [J].
EISENBERG, RA ;
CRAVEN, SY ;
WARREN, RW ;
COHEN, PL .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 80 (03) :691-697