...
首页> 外文期刊>Oncogene >Expression of a constitutively active mutant of M-Ras in normal bone marrow is sufficient for induction of a malignant mastocytosis|[sol]|mast cell leukemia, distinct from the histiocytosis|[sol]|monocytic leukemia induced by expression of activated H-Ras
【24h】

Expression of a constitutively active mutant of M-Ras in normal bone marrow is sufficient for induction of a malignant mastocytosis|[sol]|mast cell leukemia, distinct from the histiocytosis|[sol]|monocytic leukemia induced by expression of activated H-Ras

机译:在正常骨髓中的组成型活性突变体的表达足以诱导恶性乳细胞症|溶性细胞白血病,不同于通过表达活化的H-Ras诱导的单核细胞症|单核细胞症的单核细胞

获取原文
           

摘要

Expression of constitutively activated M-Ras in normal murine bone-marrow cells was sufficient to induce the factor-independent, in vitro growth and differentiation of colonies of macrophages and neutrophils, and the generation of immortal lines of factor-independent mast cells, and, upon in vivo injection of the transduced cells, a fatal mastocytosis/mast-cell leukemia. In contrast, expression of constitutively activated H-Ras in bone-marrow cells resulted in the in vitro growth, in the absence of exogenous factors, of colonies that contained only macrophages and of lines of cells resembling dendritic cells, and, upon in vivo injection of the transduced cells, a fatal histiocytosis/monocytic leukemia. Macrophages generated by bone-marrow cells expressing activated M-Ras or activated H-Ras differed morphologically, the latter appearing more activated, a difference abrogated by an inhibitor of Erk activation. Inhibition of either Erk or PI3 kinase blocked the capacity of both activated M-Ras and activated H-Ras to support proliferation and viability. However, inhibition of p38 MAPK activity suppressed proliferation of bone-marrow cells expressing activated H-Ras, but enhanced that of bone-marrow cells expressing activated M-Ras. Thus, expression of either activated M-Ras or H-Ras in normal hematopoietic cells was sufficient for transformation but each resulted in the generation of distinct lineages of cells.
机译:在普通鼠骨髓细胞中组成型活化的M-Ras的表达足以诱导巨噬细胞和中性粒细胞菌落的因子无关,体外生长和分化,以及因子无关的肥大细胞的不朽系列的产生,在体内注射转导细胞,致命乳细胞症/肥大细胞白血病。相比之下,在骨髓细胞中表达在骨髓细胞中的表达导致体外生长,在没有外源性因子的情况下含有巨噬细胞和类似树突细胞的细胞的细胞的菌落,以及在体内注射转导细胞,致命组织菌/单核细胞症/单核细胞白血病。表达活化的M-RA或活化H-RAS的骨髓细胞产生的巨噬细胞形态学上不同,后者出现更活化,ERK激活抑制剂抑制差异。 ERK或PI3激酶对ERK或PI3激酶的抑制阻断了活化的M-RA和活化的H-RA的能力,以支持增殖和活力。然而,抑制P38 MAPK活性的抑制骨髓细胞的增殖,表达活化的H-RAS,但增强了表达活化的M-RA的骨髓细胞。因此,正常造血细胞中活化的M-Ras或H-Ras的表达足以进行转化,但各自导致产生不同谱系的细胞谱系。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号