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Altered expression of Pax-5 gene in human myeloma cells.

Research Authors
Maged S Mahmoud, Naihui Huang, Masahara Nobuyoshi, Igor a. Lisukov, Hideo Tanaka, and Michio M Kawano.
Research Date
Research Journal
Blood
Research Member
Research Publisher
The American Society of Hematology.
Research Vol
87 (10)
Research Year
1996
Research_Pages
4311-4315
Research Abstract

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, 6-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 gene, 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 the 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.