CYTOPLASMIC ACCUMULATION OF THE 52 KDA RO/SS-A NUCLEAR AUTOANTIGEN IN TRANSFECTED CELL-LINES

被引:24
作者
KEECH, CL [1 ]
GORDON, TP [1 ]
MCCLUSKEY, J [1 ]
机构
[1] FLINDERS MED CTR, DEPT CLIN IMMUNOL, CTR TRANSFUS MED & IMMUNOL, BEDFORD PK, SA 5042, AUSTRALIA
关键词
D O I
10.1006/jaut.1995.0052
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The 60 kDa Ro/SS-A (Ro60) autoantigen is thought to reside predominantly in the nucleus; however, the intracellular localization of 52 kDa Ro/SS-A (Ro52) in normal cells is controversial, probably due to its low abundance. Therefore, we studied the intracellular expression and localization of the human Ro52 following transfection of a human Ro52 cDNA into cultured cell lines. Immunofluorescence staining of human (HEp-2) and mouse (LTA-5) cell transfectants with affinity-purified anti-Ro52 antibodies revealed that Ro52 antigen was most abundant in the cytoplasm and present to a lesser extent in the nucleus. This relative localization was supported by a preponderance of the Ro52 antigen in the cytoplasmic rather than nuclear fraction of enucleated cell lines detected by immunoblotting. In contrast to the Ro52 autoantigen, Ro60 and La autoantigens were mainly expressed in the nucleus of transfected cells under similar circumstances, indicating distinct localization of the intracellular pools of these autoantigens. The findings indicate that the Ro52 autoantigen lacks intrinsic signals required for nuclear localization and suggest that a significant pool of this autoantigen resides in the cytoplasm. Ro52 may therefore rely upon an association with other molecules for any specific nuclear transport. (C) Academic Press Limited
引用
收藏
页码:699 / 712
页数:14
相关论文
共 33 条
[1]   THE LA ANTIGEN SHUTTLES BETWEEN THE NUCLEUS AND THE CYTOPLASM IN CV-1 CELLS [J].
BACHMANN, M ;
PFEIFER, K ;
SCHRODER, HC ;
MULLER, WEG .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1989, 85 (02) :103-114
[2]   A 52-KD PROTEIN IS A NOVEL COMPONENT OF THE SS-A/RO ANTIGENIC PARTICLE [J].
BENCHETRIT, E ;
CHAN, EKL ;
SULLIVAN, KF ;
TAN, EM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 167 (05) :1560-1571
[3]   HUMAN RO RIBONUCLEOPROTEIN-PARTICLES - CHARACTERIZATION OF NATIVE STRUCTURE AND STABLE ASSOCIATION WITH THE LA POLYPEPTIDE [J].
BOIRE, G ;
CRAFT, J .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (04) :1182-1190
[4]  
BOZIC B, 1993, CLIN EXP IMMUNOL, V94, P227
[5]  
BUYON JP, 1994, J IMMUNOL, V152, P3675
[6]   TRANSCRIPTION-DEPENDENT COLOCALIZATION OF THE U1, U2, U4/U6, AND U5 SNRNPS IN COILED BODIES [J].
CARMOFONSECA, M ;
PEPPERKOK, R ;
CARVALHO, MT ;
LAMOND, AI .
JOURNAL OF CELL BIOLOGY, 1992, 117 (01) :1-14
[7]   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
[8]   HUMAN AUTOANTIBODY-REACTIVE EPITOPES OF SS-B/LA ARE HIGHLY CONSERVED IN COMPARISON WITH EPITOPES RECOGNIZED BY MURINE MONOCLONAL-ANTIBODIES [J].
CHAN, EKL ;
TAN, EM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 166 (06) :1627-1640
[9]   MOLECULAR DEFINITION AND SEQUENCE MOTIFS OF THE 52-KD COMPONENT OF HUMAN SS-A/RO AUTOANTIGEN [J].
CHAN, EKL ;
HAMEL, JC ;
BUYON, JP ;
TAN, EM .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (01) :68-76
[10]  
Coligan J., 1991, CURRENT PROTOCOLS IM