Shaulsky G, Goldfinger N, Peled A, Rotter V
Department of Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Proc Natl Acad Sci U S A. 1991 Oct 15;88(20):8982-6. doi: 10.1073/pnas.88.20.8982.
Wild-type p53 protein is a growth modulator whose inactivation has been found to be a key event in malignant transformation. Reconstitution of wild-type p53 in the p53-nonproducer, Abelson murine leukemia virus-transformed pre-B-cell line L12 gave rise to stably growing clones. Wild-type p53-producer derived cell lines exhibit an altered cell cycle, however. More cells with an extended G0/G1 phase were found than in the p53-nonproducer parental cell line. Furthermore, when injected into syngeneic mice, these cells induced a lower incidence of tumors and these tumors were less aggressive. Analysis of immunoglobulin expression revealed that wild-type p53 induced the expression of cytoplasmic immunoglobulin mu heavy chain. In addition, these derived cells lines exhibited increased levels of a B-cell-specific surface marker, B220. These results suggest that wild-type p53 may function as a cell differentiation factor that can induce development of pre-B cells into a more advanced stage in the pathway of B-cell maturation. In these pre-B cells, wild-type p53 may induce cell differentiation without terminal growth arrest of the cell population.
野生型p53蛋白是一种生长调节因子,其失活已被发现是恶性转化中的关键事件。在不产生p53的阿贝尔逊鼠白血病病毒转化的前B细胞系L12中重建野生型p53,产生了稳定生长的克隆。然而,野生型p53产生细胞系表现出细胞周期改变。与不产生p53的亲本细胞系相比,发现更多细胞的G0/G1期延长。此外,当将这些细胞注射到同基因小鼠中时,它们诱导的肿瘤发生率较低,并且这些肿瘤的侵袭性较小。免疫球蛋白表达分析表明,野生型p53诱导细胞质免疫球蛋白μ重链的表达。此外,这些衍生细胞系表现出B细胞特异性表面标志物B220水平的增加。这些结果表明,野生型p53可能作为一种细胞分化因子,可诱导前B细胞在B细胞成熟途径中发育到更高级阶段。在这些前B细胞中,野生型p53可能诱导细胞分化而不导致细胞群体的终末生长停滞。