Just U, Kan O, Fennelly J, Dexter T M, Spooncer E
Department of Experimental Haematology, Paterson Institute for Cancer Research, Manchester, UK.
Growth Factors. 1995;12(3):173-7. doi: 10.3109/08977199509036877.
The establishment of IL-3-dependent multipotent progenitor cell lines from Hox-2.4-expressing bone marrow cells suggests that homeobox genes may contribute to immortalization of early myeloid cells. A survey of 20 independently derived multipotent IL-3-dependent cell lines established from either src-virus-infected long-term bone marrow cultures (FDCP-mix) or Multi-CSF-virus (M3MuV)-infected bone marrow revealed that Hox-2.4 was not expressed in any of these cell lines. In addition DNA rearrangements were not observed. We conclude that activation of Hox-2.4 is not an obligatory event in the immortalization of early myeloid cells.
从表达Hox-2.4的骨髓细胞中建立白细胞介素-3依赖的多能祖细胞系表明,同源异型盒基因可能有助于早期髓样细胞的永生化。对从src病毒感染的长期骨髓培养物(FDCP-mix)或多集落刺激因子病毒(M3MuV)感染的骨髓中建立的20个独立衍生的多能白细胞介素-3依赖细胞系进行的调查显示,这些细胞系中均未检测到Hox-2.4的表达。此外,未观察到DNA重排。我们得出结论,Hox-2.4的激活并非早期髓样细胞永生化过程中的必然事件。