Grimm S, Bauer M K, Baeuerle P A, Schulze-Osthoff K
Institute of Biochemistry and Molecular Biology, Albert-Ludwigs-University, Freiburg, Germany.
J Cell Biol. 1996 Jul;134(1):13-23. doi: 10.1083/jcb.134.1.13.
Among the many target genes of the transcription factor NF-kappaB are p53 and c-myc, both of which are involved in apoptosis. This prompted us to investigate the role of NF-kappaB in this process. We report that NF-kappaB is potently activated upon serum starvation, a condition leading to apoptosis in 293 cells. Similar to Bcl-2, a transdominant-negative mutant of the NF-kappaB p65 subunit partially inhibited apoptosis, indicating a direct involvement of the transcription factor in induction of cell death. As expected, the p65 mutant suppresses kappaB-dependent gene expression. Surprisingly, transiently or stably overexpressed Bcl-2 had the same effect. The transcription inhibitory activity of the two proteins correlated with their cell death protective potential. Like Bcl-2, the related protein Bcl-xL but not Bcl-xS was able to suppress kB-dependent transcription. Bcl-2 inhibited NF-kappaB activity by an unusual mechanism. It did not prevent the release of IkappaB in the cytoplasm but down-modulated the transactivating potential of nuclear p65. These data show that NF-kappaB can participate in apoptosis. We suggest that at least part of the anti-apoptotic potential of Bcl-2 may be explained from a hitherto undiscovered activity of Bcl-2 in controlling nuclear gene expression.
转录因子NF-κB的众多靶基因中包括p53和c-myc,二者均参与细胞凋亡过程。这促使我们研究NF-κB在此过程中的作用。我们报道,血清饥饿时NF-κB被强烈激活,血清饥饿会导致293细胞发生凋亡。与Bcl-2相似,NF-κB p65亚基的反式显性负性突变体部分抑制了细胞凋亡,这表明该转录因子直接参与细胞死亡的诱导。正如预期的那样,p65突变体抑制κB依赖性基因表达。令人惊讶的是,瞬时或稳定过表达的Bcl-2也有同样的效果。这两种蛋白的转录抑制活性与其细胞死亡保护潜能相关。与Bcl-2一样,相关蛋白Bcl-xL而非Bcl-xS能够抑制κB依赖性转录。Bcl-2通过一种不同寻常的机制抑制NF-κB活性。它并未阻止细胞质中IkappaB的释放,而是下调了核p65的反式激活潜能。这些数据表明NF-κB可参与细胞凋亡。我们认为,Bcl-2至少部分的抗凋亡潜能可能是由于其在控制核基因表达方面存在一种迄今未被发现的活性。