HRF20/CD59 COMPLEMENT REGULATORY PROTEIN EXPRESSION IS PHENOTYPE-DEPENDENT AND INDUCIBLE BY THE HYPOMETHYLATING AGENT 5-AZACYTIDINE ON BURKITTS-LYMPHOMA CELL-LINES

被引:4
作者
KURAYA, M
MINAROVITS, J
OKADA, H
KLEIN, E
机构
[1] KAROLINSKA INST,DEPT TUMOR BIOL,BOX 60400,S-10401 STOCKHOLM 60,SWEDEN
[2] NATL INST HYG,MICROBIOL RES GRP,BUDAPEST,HUNGARY
[3] NAGOYA CITY UNIV,SCH MED,DEPT MOLEC BIOL,NAGOYA,AICHI 467,JAPAN
关键词
CD59/HRF20; EPSTEIN-BARR VIRUS; BURKITTS LYMPHOMA LINE; B-LYMPHOCYTE; DNA METHYLATION;
D O I
10.1016/0165-2478(93)90129-P
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We studied the expression of the 20-kDa homologous restriction factor (CD59/HRF20), a complement regulatory protein, on two subsets of blood derived B cells and on Burkitt's lymphoma lines. Both low-density (activated) and high-density (resting) B cell populations expressed high levels of CD59. CD59 was detectable, however, only on a minority of cells or not at all on three Epstein-Barr virus (EBV)-negative BL lines (BL41, BL28 and DG75) and on clones of an EBV-positive BL line (Mutu) that phenotypically resembled resting B lymphocytes. On the other hand, CD59 was detected at high or medium levels on Mutu cells which had a lymphoblastoid cell-like phenotype. Expression of CD59 was up-regulated by 5-azacytidine, a drug inhibiting cytosine methylation, on CD59-negative cell lines. Induction was accompanied by a partial hypomethylation in the 5' region of CD59 coding sequences.
引用
收藏
页码:35 / 39
页数:5
相关论文
共 16 条
[1]   THE ESSENTIALS OF DNA METHYLATION [J].
BIRD, A .
CELL, 1992, 70 (01) :5-8
[2]   CD59, AN LY-6-LIKE PROTEIN EXPRESSED IN HUMAN LYMPHOID-CELLS, REGULATES THE ACTION OF THE COMPLEMENT MEMBRANE ATTACK COMPLEX ON HOMOLOGOUS CELLS [J].
DAVIES, A ;
SIMMONS, DL ;
HALE, G ;
HARRISON, RA ;
TIGHE, H ;
LACHMANN, PJ ;
WALDMANN, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (03) :637-654
[3]   DISTINCTION BETWEEN BURKITT-LYMPHOMA SUBGROUPS BY MONOCLONAL-ANTIBODIES - RELATIONSHIPS BETWEEN ANTIGEN EXPRESSION AND TYPE OF CHROMOSOMAL TRANSLOCATION [J].
EHLINHENRIKSSON, B ;
KLEIN, G .
INTERNATIONAL JOURNAL OF CANCER, 1984, 33 (04) :459-463
[4]   DIFFERENT EPSTEIN-BARR VIRUS-B CELL-INTERACTIONS IN PHENOTYPICALLY DISTINCT CLONES OF A BURKITTS-LYMPHOMA CELL-LINE [J].
GREGORY, CD ;
ROWE, M ;
RICKINSON, AB .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :1481-1495
[5]   ISOLATION AND CHARACTERIZATION OF A MEMBRANE-PROTEIN FROM NORMAL HUMAN-ERYTHROCYTES THAT INHIBITS REACTIVE LYSIS OF THE ERYTHROCYTES OF PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA [J].
HOLGUIN, MH ;
FREDRICK, LR ;
BERNSHAW, NJ ;
WILCOX, LA ;
PARKER, CJ .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (01) :7-17
[6]   EXPRESSION OF THE COMPLEMENT REGULATORY PROTEINS CD21, CD55 AND CD59 ON BURKITT-LYMPHOMA LINES - THEIR ROLE IN SENSITIVITY TO HUMAN SERUM-MEDIATED LYSIS [J].
KURAYA, M ;
YEFENOF, E ;
KLEIN, G ;
KLEIN, E .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (07) :1871-1876
[7]  
Maniatis T., 1982, MOL CLONING
[8]  
MERI S, 1990, IMMUNOLOGY, V71, P1
[9]   HOST-CELL PHENOTYPE-DEPENDENT METHYLATION PATTERNS OF EPSTEIN-BARR-VIRUS DNA [J].
MINAROVITS, J ;
MINAROVITSKORMUTA, S ;
EHLINHENRIKSSON, B ;
FALK, K ;
KLEIN, G ;
ERNBERG, I .
JOURNAL OF GENERAL VIROLOGY, 1991, 72 :1591-1599
[10]   20KDA HOMOLOGOUS RESTRICTION FACTOR OF COMPLEMENT RESEMBLES T-CELL ACTIVATING PROTEIN [J].
OKADA, H ;
NAGAMI, Y ;
TAKAHASHI, K ;
OKADA, N ;
HIDESHIMA, T ;
TAKIZAWA, H ;
KONDO, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 162 (03) :1553-1559