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ETV6/CBFA2(TEL/AML1)的表达不足以在体外转化造血细胞系或在体内诱发血液疾病。

The expression of ETV6/CBFA2 (TEL/AML1) is not sufficient for the transformation of hematopoietic cell lines in vitro or the induction of hematologic disease in vivo.

作者信息

Andreasson P, Schwaller J, Anastasiadou E, Aster J, Gilliland D G

机构信息

Division of Hematology, Brigham and Women's Hospital, 4 Blackfan Circle, Boston, MA, USA.

出版信息

Cancer Genet Cytogenet. 2001 Oct 15;130(2):93-104. doi: 10.1016/s0165-4608(01)00518-0.

DOI:10.1016/s0165-4608(01)00518-0
PMID:11675129
Abstract

ETV6/CBFA2 (TEL/AML1) is the most frequent genetic abnormality associated with acute lymphoblastic leukemias in children, and is associated with a favorable prognosis. To investigate the influence of ETV6/CBFA2 on cellular transformation, the fusion gene was cloned into a murine ecotropic retroviral vector and transduced into IL-3-dependent Ba/F3 and 32Dcl.3 and IL-7-dependent IxN/2b murine hematopoietic cell lines. Different variants of ETV6/CBFA2, corresponding to CBFA2 alternatively spliced variants, and the reciprocal product CBFA2/ETV6, were stably expressed in each of these cell lines. However, although Western blot analysis demonstrated expression of each variant, none of the stable cell lines expressing CBFA2/ETV6 or the variants conferred factor-independent growth. We further investigated the effect of ETV6/CBFA2 expression in vivo by generating transgenic mice in which expression of the fusion was directed to lymphoid cells using the immunoglobulin heavy chain enhancer/promoter. Four founder mice were identified showing transmission and expression of the chimeric product. The mice were bred for five generations and followed for more than 24 months. The mice did not develop a malignant hematologic disorder, nor did they display histopathologic, morphologic, or immunophenotypic abnormalities, although ETV6/CBFA2 expression was confirmed in each line. We conclude that the expression of ETV6/CBFA2 alone is not sufficient for induction of growth factor independence in hematopoietic cell lines or hematologic disease in transgenic mice.

摘要

ETV6/CBFA2(TEL/AML1)是与儿童急性淋巴细胞白血病相关的最常见基因异常,且与预后良好相关。为了研究ETV6/CBFA2对细胞转化的影响,将该融合基因克隆到鼠嗜异性逆转录病毒载体中,并转导至依赖白细胞介素-3的Ba/F3和32Dcl.3以及依赖白细胞介素-7的IxN/2b鼠造血细胞系。ETV6/CBFA2的不同变体,对应于CBFA2的可变剪接变体,以及反向产物CBFA2/ETV6,在这些细胞系中均稳定表达。然而,尽管蛋白质免疫印迹分析证实了每个变体的表达,但表达CBFA2/ETV6或这些变体的稳定细胞系均未赋予细胞因子非依赖性生长特性。我们通过构建转基因小鼠进一步研究ETV6/CBFA2在体内的作用,在这些小鼠中利用免疫球蛋白重链增强子/启动子将融合基因的表达定向至淋巴细胞。鉴定出4只奠基小鼠,显示嵌合产物的传递和表达。这些小鼠繁殖了5代,并随访超过24个月。尽管在每个品系中均证实了ETV6/CBFA2的表达,但这些小鼠并未发生恶性血液系统疾病,也未表现出组织病理学、形态学或免疫表型异常。我们得出结论,单独的ETV6/CBFA2表达不足以诱导造血细胞系中生长因子非依赖性或转基因小鼠发生血液系统疾病。

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