Chylicki K, Ehinger M, Svedberg H, Gullberg U
Department of Hematology, Lund University, Sweden.
Cell Growth Differ. 2000 Nov;11(11):561-71.
The p53 tumor suppressor protein can induce both apoptosis and cell cycle arrest. Moreover, we and others have shown previously that p53 is a potent mediator of differentiation. For example, expression of ptsp53, a temperature-inducible form of p53, induces differentiation of leukemic monoblastic U-937 cells. The functions of p53 have for long been believed to be dependent on the transactivating capacity of p53. However, recent data show that both p53-induced cell cycle arrest and apoptosis can be induced independently of p53-mediated transcriptional activation, indicating alternative pathways for p53-induced apoptosis and cell cycle arrest. The bcl-2 proto-oncogene contributes to the development of certain malignancies, probably by inhibition of apoptosis. Interestingly, Bcl-2 has been shown to inhibit p53-mediated apoptosis as well as p53-mediated transcriptional activation. Asking whether Bcl-2 would interfere with the p53-mediated differentiation of U-937 cells, we stably transfected bcl-2 to U-937 cells inducibly expressing p53. Although the established Bcl-2-expressing clones were resistant to p53-mediated apoptosis, we did not observe any interference of Bcl-2 with the p53-mediated differentiation, suggesting separable pathways for p53 in mediating apoptosis and differentiation of U-937 cells. Neither did expression of Bcl-2 interfere with p53-induced expression of endogenous p21, suggesting that p53-induced differentiation might be dependent on the transcriptional activity of p53. To further investigate whether the p53-mediated differentiation of U-937 cells depends on the transcriptional activity of p53, we overexpressed transactivation-deficient p53, a transcriptionally inactive p53 mutant in these cells. However, in contrast to the effects of wild-type p53, expression of trans-activation-deficient p53 did neither induce signs of apoptosis nor of differentiation in U-937 cells. Our results indicate that the transcriptional activity of p53 is essential both for p53-mediated apoptosis and differentiation of U-937 cells.
p53肿瘤抑制蛋白既能诱导细胞凋亡,也能使细胞周期停滞。此外,我们和其他人之前已经表明,p53是分化的有效调节因子。例如,ptsp53(一种温度诱导型p53)的表达可诱导白血病单核细胞U - 937细胞分化。长期以来,人们一直认为p53的功能依赖于其反式激活能力。然而,最近的数据表明,p53诱导的细胞周期停滞和细胞凋亡都可以独立于p53介导的转录激活而被诱导,这表明p53诱导细胞凋亡和细胞周期停滞存在替代途径。bcl - 2原癌基因可能通过抑制细胞凋亡促进某些恶性肿瘤的发展。有趣的是,Bcl - 2已被证明能抑制p53介导的细胞凋亡以及p53介导的转录激活。为了探究Bcl - 2是否会干扰p53介导的U - 937细胞分化,我们将bcl - 2稳定转染到可诱导表达p53的U - 937细胞中。尽管已建立的表达Bcl - 2的克隆对p53介导的细胞凋亡具有抗性,但我们未观察到Bcl - 2对p53介导的分化有任何干扰,这表明p53在介导U - 937细胞凋亡和分化方面存在可分离的途径。Bcl - 2的表达也未干扰p53诱导的内源性p21的表达,这表明p53诱导的分化可能依赖于p53的转录活性。为了进一步研究p53介导的U - 937细胞分化是否依赖于p53的转录活性,我们在这些细胞中过表达了反式激活缺陷型p53(一种转录无活性的p53突变体)。然而,与野生型p53的作用相反,反式激活缺陷型p53的表达在U - 937细胞中既未诱导细胞凋亡迹象,也未诱导分化迹象。我们的结果表明,p53的转录活性对于p53介导的U - 937细胞凋亡和分化至关重要。