期刊
CRITICAL CARE MEDICINE
卷 28, 期 4, 页码 N100-N104出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/00003246-200004001-00012
关键词
NF-kappa B; transcription factors; cyclic AMP responsive element-binding protein (CREB); CREB-binding protein (CBP); cytokines; neutrophils; acute respiratory distress syndrome; sepsis; endotoxemia; hemorrhage; reactive oxygen intermediates; catecholamines
资金
- NHLBI NIH HHS [HL50284] Funding Source: Medline
Binding sites for the transcriptional regulatory factor nuclear factor kappa B (NF-kappa B) are present in the promoter regions of many of the proinflammatory cytokines and immunoregulatory mediators important in inducing acute inflammatory responses associated with critical illnesses. Because increased activation of NF-kappa B leads to enhanced expression of these proinflammatory mediators, NF-kappa B activation may be a central event in the development of multiple organ dysfunction associated with infection, blood loss, and ischemia-reperfusion injury. NF-kappa B is normally retained in the cytoplasm through its association with the inhibitory molecule I kappa B. Phosphorylation, ubiquination, and proteolysis of I kappa B allows NF-kappa B to translocate to the nucleus and induce transcription, once associated with the transcriptional cofactor CBP. The transcriptional activity of NF-kappa B can be regulated at multiple steps, including the amount of I kappa B present, NF-kappa B subunit composition, and competition for CBP binding. Because of the central role that NF-kappa B occupies in modulating immunoregulatory responses, further understanding of its regulation will be important in designing future therapies able to prevent or minimize acute inflammatory injury associated with critical illness.
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