Klinken S P, Alexander W S, Adams J M
Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Parkville, Victoria, Australia.
Cell. 1988 Jun 17;53(6):857-67. doi: 10.1016/s0092-8674(88)90309-1.
Hemopoietic lineage commitment can be breached by concomitant expression of the c-myc and v-raf oncogenes. Switching to the myeloid lineage occurred frequently when B lineage cells, from either lymphomas or preleukemia bone marrow cells of Emu-myc transgenic mice, were infected with a retrovirus bearing v-raf. Cloned pre-B and B cell lines changed into either mature or immature macrophages as assessed by morphology, adherence, phagocytic activity, surface markers, and lysozyme production, but retained clonotypic immunoglobulin gene rearrangements. Although expression of the Emu-myc transgene was reduced or abolished in the more differentiated lines, the lines remained tumorigenic. The converted lines produced the myeloid growth factor GM-CSF, and most had karyotypic alterations. These results suggest that constitutive myc plus raf expression can provoke genetic reprogramming in lymphocytes.
c-myc和v-raf癌基因的同时表达可突破造血谱系的定向分化。当来自Emu-myc转基因小鼠淋巴瘤或白血病前期骨髓细胞的B谱系细胞感染携带v-raf的逆转录病毒时,向髓系谱系的转变频繁发生。通过形态学、贴壁能力、吞噬活性、表面标志物和溶菌酶产生评估,克隆的前B细胞和B细胞系转变为成熟或不成熟的巨噬细胞,但保留了克隆型免疫球蛋白基因重排。尽管在分化程度更高的细胞系中Emu-myc转基因的表达降低或消失,但这些细胞系仍具有致瘤性。转化后的细胞系产生髓系生长因子GM-CSF,且大多数具有核型改变。这些结果表明,持续的myc加raf表达可引发淋巴细胞的基因重编程。