Carta Sonia, Castellani Patrizia, Delfino Laura, Tassi Sara, Venè Roberta, Rubartelli Anna
Cell Biology Unit, Istituto Nazionale per la Ricerca sul Cancro, 16132 Genova, Italy.
J Leukoc Biol. 2009 Sep;86(3):549-55. doi: 10.1189/jlb.1008598. Epub 2009 Jun 29.
Inflammation is deeply entangled with redox modulation. Triggering of PRRs on inflammatory cells induces ROS generation. As a consequence, activated cells mount antioxidant responses to counteract the possible harmful effects of oxidation. Therefore, when repair is completed, homeostasis is restored. Here, we describe some recent results showing that an exuberant antioxidant response to pro-oxidant inflammatory stimuli modifies not only the intra- but also the extracellular redox and contributes to the outcome of the inflammatory process. In particular, the role of redox modulation in IL-1beta secretion, in B lymphocyte differentiation to plasma cells, and in tumor progression will be discussed, and the potential consequences of extracellular redox alterations on DAMP activity will be considered.
炎症与氧化还原调节密切相关。炎性细胞上模式识别受体(PRRs)的激活会诱导活性氧(ROS)的产生。因此,被激活的细胞会启动抗氧化反应以抵消氧化可能带来的有害影响。所以,当修复完成时,内环境稳态得以恢复。在此,我们描述一些近期的研究结果,这些结果表明,对促氧化炎症刺激的过度抗氧化反应不仅会改变细胞内的氧化还原状态,还会改变细胞外的氧化还原状态,并影响炎症过程的结果。特别是,我们将讨论氧化还原调节在白细胞介素 -1β(IL-1β)分泌、B淋巴细胞向浆细胞分化以及肿瘤进展中的作用,并考虑细胞外氧化还原改变对损伤相关分子模式(DAMP)活性的潜在影响。