Shishodia Shishir, Aggarwal Bharat B
Cytokine Research Section, Department of Bioimmunotherapy, The University of Texas M. D. Anderson Cancer Center, Box 143, 1515 Holcombe Boulevard, Houston, Texas 77030, USA.
J Biochem Mol Biol. 2002 Jan 31;35(1):28-40. doi: 10.5483/bmbrep.2002.35.1.028.
Apoptosis is a mode of cell death that plays an important role in both pathological and physiological processes. Research during the last decade has delineated the entire machinery needed for cell death, and its constituents were found to pre-exist in cells. The apoptotic cascade is triggered when cells are exposed to an apoptotic stimulus. It has been known for several years that inhibitors of protein synthesis can potentiate apoptosis that is induced by cytokines and other inducers. Until 1996, it was not understood why protein synthesis inhibitors potentiate apoptosis. Then three reports appeared that suggested the role of the transcription factor NF-kappaB activation in protecting the cells from TNF-induced apoptosis. Since then several proteins have been identified that are regulated by NF-kappaB and are involved in cell survival, proliferation, and protection from apoptosis. It now seems that when a cell is attacked by an apoptotic stimulus, the cell responds first by activating anti-apoptotic mechanisms, which may or may not be followed by apoptosis. Whether or not a cell undergoes proliferation, the survival, or apoptosis, appears to involve a balance between the two mechanisms. Inhibitors of protein synthesis seem to suppress the appearance of protein that are involved in anti-apoptosis. The present review discusses how NF-kappaB controls apoptosis.
细胞凋亡是一种细胞死亡方式,在病理和生理过程中均发挥重要作用。过去十年间的研究已阐明细胞死亡所需的整个机制,且发现其组成成分在细胞中预先存在。当细胞暴露于凋亡刺激时,凋亡级联反应被触发。多年来已知蛋白质合成抑制剂可增强由细胞因子和其他诱导剂诱导的细胞凋亡。直到1996年,人们才明白蛋白质合成抑制剂为何会增强细胞凋亡。随后出现的三篇报道表明转录因子NF-κB激活在保护细胞免受肿瘤坏死因子诱导的细胞凋亡中所起的作用。从那时起,已鉴定出几种受NF-κB调控且参与细胞存活、增殖及抗凋亡保护的蛋白质。现在看来,当细胞受到凋亡刺激攻击时,细胞首先通过激活抗凋亡机制做出反应,随后可能发生或不发生细胞凋亡。细胞是否进行增殖、存活或凋亡,似乎涉及这两种机制之间的平衡。蛋白质合成抑制剂似乎会抑制参与抗凋亡的蛋白质的出现。本综述讨论了NF-κB如何控制细胞凋亡。