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人骨髓瘤细胞中Pax-5基因的表达改变

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

作者信息

Mahmoud M S, Huang N, Nobuyoshi M, Lisukov I A, Tanaka H, Kawano M M

机构信息

Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Japan.

出版信息

Blood. 1996 May 15;87(10):4311-5.

PMID:8639790
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, 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.

摘要

近期对浆细胞的表型分析表明,正常浆细胞确实表达B细胞谱系特异性分子CD19,但其恶性对应物(骨髓瘤细胞)不表达CD19。为阐明骨髓瘤细胞上CD19抗原缺失的意义,我们首先比较了B细胞、正常浆细胞、骨髓瘤细胞系和原发性骨髓瘤细胞中CD19和Pax-5基因的表达情况,因为据报道Pax-5基因编码CD19基因表达所必需的转录因子——B细胞特异性激活蛋白(BSAP)。在那些原发性骨髓瘤细胞和细胞系中均未检测到CD19和Pax-5 mRNA,而正常浆细胞确实同时表达CD19和Pax-5 mRNA。此外,我们通过凝胶迁移试验证实,在CD19阴性的骨髓瘤细胞系(KMS-5)的核提取物中未检测到BSAP结合活性,但在CD19阳性的B细胞系(Raji)中检测到了该活性。我们进一步检测了E2A和Id基因的表达,因为E2A和Id分别被认为是Pax-5基因表达的正调控因子和负调控因子。然而,在骨髓瘤细胞和正常浆细胞之间未观察到这些E2A和Id-2基因表达的显著差异。因此,这些数据表明,是Pax-5表达的改变而非E2A或Id的改变导致了人类骨髓瘤细胞中CD19表达的缺失,尽管Pax-5基因表达改变的潜在机制仍有待阐明。

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