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Spi-1/PU.1转基因小鼠会发生多步骤的红白血病。

Spi-1/PU.1 transgenic mice develop multistep erythroleukemias.

作者信息

Moreau-Gachelin F, Wendling F, Molina T, Denis N, Titeux M, Grimber G, Briand P, Vainchenker W, Tavitian A

机构信息

INSERM U248, Institut Curie, Paris, France.

出版信息

Mol Cell Biol. 1996 May;16(5):2453-63. doi: 10.1128/MCB.16.5.2453.

Abstract

Insertional mutagenesis of the spi-1 gene is associated with the emergence of malignant proerythroblasts during Friend virus-induced acute erythroleukemia. To determine the role of spi-1/PU.1 in the genesis of leukemia, we generated spi-1 transgenic mice. In one founder line the transgene was overexpressed as an unexpected-size transcript in various mouse tissues. Homozygous transgenic animals gave rise to live-born offspring, but 50% of the animals developed a multistep erythroleukemia within 1.5 to 6 months of birth whereas the remainder survived without evidence of disease. At the onset of the disease, mice became severely anemic. Their hematopoietic tissues were massively invaded with nontumorigenic proerythroblasts that express a high level of Spi-1 protein. These transgenic proerythroblasts are partially blocked in differentiation and strictly dependent on erythropoietin for their proliferation both in vivo and in vitro. A complete but transient regression of the disease was observed after erythrocyte transfusion, suggesting that the constitutive expression of spi-1 is related to the block of the differentiation of erythroid precursors. At relapse, erythropoietin-independent malignant proerythroblasts arose. Growth factor autonomy could be partially explained by the autocrine secretion of erythropoietin; however, other genetic events appear to be necessary to confer the full malignant phenotype. These results reveal that overexpression of spi-1 is essential for malignant erythropoiesis and does not alter other hematopoietic lineages.

摘要

在弗氏病毒诱导的急性红白血病中,spi-1基因的插入诱变与恶性成红细胞的出现有关。为了确定spi-1/PU.1在白血病发生中的作用,我们培育了spi-1转基因小鼠。在一个奠基者品系中,转基因作为一种意外大小的转录本在各种小鼠组织中过表达。纯合转基因动物能产生存活的后代,但50%的动物在出生后1.5至6个月内发展为多步骤红白血病,而其余动物存活且无疾病迹象。在疾病发作时,小鼠出现严重贫血。它们的造血组织被大量表达高水平Spi-1蛋白的非致瘤性成红细胞侵入。这些转基因成红细胞在分化过程中部分受阻,并且在体内和体外增殖都严格依赖于促红细胞生成素。红细胞输血后观察到疾病完全但短暂的消退,这表明spi-1的组成型表达与红系前体细胞分化受阻有关。复发时,出现了不依赖促红细胞生成素的恶性成红细胞。生长因子自主性部分可由促红细胞生成素的自分泌分泌来解释;然而,似乎还需要其他遗传事件来赋予完全的恶性表型。这些结果表明,spi-1的过表达对恶性红细胞生成至关重要,且不会改变其他造血谱系。

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