Signaling Systems Laboratory, Department of Chemistry and Biochemistry, University of California - San Diego, La Jolla, CA, USA.
Wiley Interdiscip Rev Syst Biol Med. 2009 Jul-Aug;1(1):107-115. doi: 10.1002/wsbm.30.
The NF-κB transcription factor is a critical regulator of the immune system, and is responsive to a large number of stimuli. Different stimuli engage signaling pathways to activate NF-κB, and effect distinct cellular responses. Mathematical modeling of the NF-κB network has been useful in studying the dynamic and cross-talk regulation of NF-κB. In this review, we discuss the regulation of NF-κB activity in response to different types of stimuli, including inflammatory signals, developmental cues, metabolic stress, and DNA damage. The distinct molecular mechanisms engaged in each pathway for activating and terminating NF-κB activity are discussed. In addition, we summarize the evidence for cross-talk mechanisms that allow for different stimuli to be integrated within the NF-κB signaling module to produce synergistic or qualitatively different signaling outcomes.
NF-κB 转录因子是免疫系统的关键调节因子,对大量刺激作出反应。不同的刺激通过信号通路激活 NF-κB,并产生不同的细胞反应。NF-κB 网络的数学建模在研究 NF-κB 的动态和串扰调节方面非常有用。在这篇综述中,我们讨论了 NF-κB 活性对不同类型刺激的反应调节,包括炎症信号、发育线索、代谢应激和 DNA 损伤。讨论了每条途径中用于激活和终止 NF-κB 活性的不同分子机制。此外,我们总结了允许不同刺激在 NF-κB 信号模块内整合以产生协同或定性不同信号结果的串扰机制的证据。