Zong W X, Farrell M, Bash J, Gélinas C
Center for Advanced Biotechnology and Medicine, University of Medicine and Dentistry of New Jersey, Piscataway 08854-5638, USA.
Oncogene. 1997 Aug 18;15(8):971-80. doi: 10.1038/sj.onc.1201266.
The v-Rel oncoprotein belongs to the Rel/NF-kappaB family of transcription factors. It transforms chicken lymphoid cells in vitro and induces fatal lymphomas in vivo. In this study, we used a tetracycline-regulated system to characterize the role of v-Rel in cell transformation. We show that the continued expression of v-Rel is necessary to maintain the viability of transformed lymphoid cells and enables primary spleen cells to escape apoptosis in vitro culture. In agreement with a possible role for v-Rel in the inhibition of programmed cell death, its inducible expression in HeLa cells prevented TNFalpha-induced apoptosis. While the repression of v-Rel was accompanied by the rapid degradation of IkappaBalpha, changes in the steady-state levels of the apoptosis inhibitors Bcl-2 and Bcl-X(L) were only observed following the onset of cell death in transformed lymphoid cells. This suggests that the anti-apoptotic activity of v-Rel may affect other apoptosis inhibitors or other factors in the death pathway. Together, these findings demonstrate that v-Rel blocks apoptosis and suggest that this activity may be an important component of its transforming function.
v-Rel癌蛋白属于Rel/NF-κB转录因子家族。它在体外可转化鸡淋巴细胞,并在体内诱导致命性淋巴瘤。在本研究中,我们使用四环素调控系统来阐明v-Rel在细胞转化中的作用。我们发现,持续表达v-Rel对于维持转化淋巴细胞的活力是必需的,并且能使原代脾细胞在体外培养中逃避凋亡。与v-Rel在抑制程序性细胞死亡中可能发挥的作用一致,其在HeLa细胞中的可诱导表达可防止TNFα诱导的凋亡。虽然v-Rel的抑制伴随着IκBα的快速降解,但仅在转化淋巴细胞发生细胞死亡后才观察到凋亡抑制剂Bcl-2和Bcl-X(L)稳态水平的变化。这表明v-Rel的抗凋亡活性可能影响死亡途径中的其他凋亡抑制剂或其他因子。总之,这些发现表明v-Rel可阻断凋亡,并提示该活性可能是其转化功能的重要组成部分。