Altered expression of Pax-5 gene in human myeloma cells

被引:42
作者
Mahmoud, MS [1 ]
Huang, NH [1 ]
Nobuyoshi, M [1 ]
Lisukov, IA [1 ]
Tanaka, H [1 ]
Kawano, MM [1 ]
机构
[1] HIROSHIMA UNIV, RES INST RADIAT BIOL & MED,DEPT HEMATOL & ONCOL, MYELOMA STUDY GRP,MINAMI KU, HIROSHIMA 734, JAPAN
关键词
D O I
10.1182/blood.V87.10.4311.bloodjournal87104311
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recent phenotypic analysis of plasma cells showed that normal plasma cells do express the B-cell lineage-specific molecule CD19, but their malignant counterpart (myeloma cells) are CD19(-). To clarify the meaning of loss of CD19 antigen on myeloma cells, we first compared the expression of CD19 and Pax-5 genes among B cells, normal plasma cells, myeloma cell lines, and primary myeloma cells, because the Pax-5 gene was reported to encode the transcriptional factor, B-cell-specific activating protein (BSAP), necessary for CD19 gene expression. Neither CD19 nor Pax-5 mRNA could be detected in those primary myeloma cells and cell lines, whereas normal plasma cells did express both CD19 and Pax-5 mRNA. Furthermore, we could confirm that BSAP-binding activity was not detected in the nuclear extract from CD19(-) myeloma cell line (KMS-5) but was detected in CD19(+) B-cell line (Raji) by gel-shift assay. We further examined the expression of E2A and Id genes, because E2A and Id are considered to be positive and negative regulators in the expression of Pax-5 gene, respectively. However, no significant differences in the expression of these E2A and Id-2 genes could be observed between myeloma cells and normal plasma cells. Therefore, these data suggest that the altered expression of Pax-5, but not E2A or Id, is responsible for the loss of CD19 expression in human myeloma cells, although the underlying mechanism of the altered Pax-5 gene expression remains to be clarified. (C) 1996 by The American Society of Hematology.
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页码:4311 / 4315
页数:5
相关论文
共 20 条
[11]  
KAWANO MM, 1995, BLOOD, V85, P487
[12]  
KAWANO MM, 1993, BLOOD, V82, P564
[13]   MOLECULAR MECHANISMS REGULATING CD19, CD20 AND CD22 GENE-EXPRESSION [J].
KEHRL, JH ;
RIVA, A ;
WILSON, GL ;
THEVENIN, C .
IMMUNOLOGY TODAY, 1994, 15 (09) :432-436
[14]   THE PROMOTER OF THE CD19 GENE IS A TARGET FOR THE B-CELL-SPECIFIC TRANSCRIPTION FACTOR BSAP [J].
KOZMIK, Z ;
WANG, S ;
DORFLER, P ;
ADAMS, B ;
BUSSLINGER, M .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (06) :2662-2672
[15]  
NADLER LM, 1983, J IMMUNOL, V131, P244
[16]   RAPID DETECTION OF OCTAMER BINDING-PROTEINS WITH MINI-EXTRACTS, PREPARED FROM A SMALL NUMBER OF CELLS [J].
SCHREIBER, E ;
MATTHIAS, P ;
MULLER, MM ;
SCHAFFNER, W .
NUCLEIC ACIDS RESEARCH, 1989, 17 (15) :6419-6419
[17]   CONSTITUTIVE EXPRESSION OF THE ID1 GENE IMPAIRS MOUSE B-CELL DEVELOPMENT [J].
SUN, XH .
CELL, 1994, 79 (05) :893-900
[18]   ID PROTEINS ID1 AND ID2 SELECTIVELY INHIBIT DNA-BINDING BY ONE CLASS OF HELIX-LOOP-HELIX PROTEINS [J].
SUN, XH ;
COPELAND, NG ;
JENKINS, NA ;
BALTIMORE, D .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (11) :5603-5611
[19]   COMPLETE BLOCK OF EARLY B-CELL DIFFERENTIATION AND ALTERED PATTERNING OF THE POSTERIOR MIDBRAIN IN MICE LACKING PAX5/BSAP [J].
URBANEK, P ;
WANG, ZQ ;
FETKA, I ;
WAGNER, EF ;
BUSSLINGER, M .
CELL, 1994, 79 (05) :901-912
[20]   THE HELIX-LOOP-HELIX GENE E2A IS REQUIRED FOR B-CELL FORMATION [J].
ZHUANG, Y ;
SORIANO, P ;
WEINTRAUB, H .
CELL, 1994, 79 (05) :875-884