Fadeel B, Zhivotovsky B, Orrenius S
Institute of Environmental Medicine, Division of Toxicology, Karolinska Institutet, 171 77 Stockholm, Sweden.
FASEB J. 1999 Oct;13(13):1647-57. doi: 10.1096/fasebj.13.13.1647.
Members of the expanding family of Bcl-2-like proteins have emerged as important regulators of programmed cell death, and recent studies have unearthed numerous mechanisms for regulating the function of these death agonists and antagonists. In addition to the transcriptional control of gene expression, these mechanisms include posttranslational events such as phosphorylation, proteolysis, and the induction of conformational changes, which may either activate or inactivate these molecules. Interaction with homologous and nonhomologous proteins and specific subcellular targeting of Bcl-2-like proteins are other means of fine-tuning the cellular response to noxious stimuli. Recently, considerable attention has turned to the regulation of so-called BH3-only molecules, which appear to act as stress sensors that relay signals to other pro- or antiapoptotic family members. We discuss how the regulation of these apoptosis regulators may control the ultimate fate of the cell.
不断扩大的Bcl-2样蛋白家族成员已成为程序性细胞死亡的重要调节因子,最近的研究揭示了许多调节这些死亡激动剂和拮抗剂功能的机制。除了基因表达的转录控制外,这些机制还包括翻译后事件,如磷酸化、蛋白水解和构象变化的诱导,这些变化可能激活或失活这些分子。与同源和非同源蛋白的相互作用以及Bcl-2样蛋白的特定亚细胞定位是微调细胞对有害刺激反应的其他方式。最近,人们相当关注所谓的仅含BH3结构域分子的调节,这些分子似乎充当应激传感器,将信号传递给其他促凋亡或抗凋亡家族成员。我们讨论了这些凋亡调节因子的调节如何控制细胞的最终命运。