Daley G Q, Baltimore D
Whitehead Institute for Biomedical Research, Cambridge Center, MA 02142.
Proc Natl Acad Sci U S A. 1988 Dec;85(23):9312-6. doi: 10.1073/pnas.85.23.9312.
The P210bcr/abl protein is associated with virtually every case of human chronic myelogenous leukemia. Unlike the related P160gag/v-abl oncogene product of Abelson murine leukemia virus, P210bcr/abl does not transform NIH 3T3 fibroblasts. To assess whether P210bcr/abl might transform hematopoietic cell types, retroviral constructs encoding P210bcr/abl were used to infect the bone marrow-derived interleukin 3-dependent Ba/F3 cell line. As for P160gag/v-abl, cell lines expressing P210bcr/abl were growth factor independent and tumorigenic in nude mice. No evidence for autocrine production of interleukin 3 by factor-independent cell lines was found. These experiments establish that P210bcr/abl can transform hematopoietic cell types to tumorigenicity.
P210bcr/abl蛋白几乎与每一例人类慢性粒细胞白血病相关。与艾贝尔森鼠白血病病毒的相关P160gag/v-abl癌基因产物不同,P210bcr/abl不能转化NIH 3T3成纤维细胞。为了评估P210bcr/abl是否可能转化造血细胞类型,编码P210bcr/abl的逆转录病毒构建体被用于感染源自骨髓的白细胞介素3依赖型Ba/F3细胞系。与P160gag/v-abl一样,表达P210bcr/abl的细胞系在无生长因子的情况下生长,并且在裸鼠中具有致瘤性。未发现非依赖因子的细胞系自分泌白细胞介素3的证据。这些实验证实P210bcr/abl可将造血细胞类型转化为致瘤性。