Berger Thorsten, Saunders Mary E, Mak Tak W
The Campbell Family Institute for Breast Cancer Research and Ontario Cancer Institute, University Health Network, Toronto, Ontario M5G 2C1, Canada.
The Campbell Family Institute for Breast Cancer Research and Ontario Cancer Institute, University Health Network, Toronto, Ontario M5G 2C1, Canada
Cold Spring Harb Symp Quant Biol. 2013;78:141-7. doi: 10.1101/sqb.2013.78.020107.
Uncontrolled inflammation is a feature of autoimmune diseases and autoinflammatory syndromes and may promote tumorigenesis. Thus, identifying molecules that regulate the signaling pathways triggering, mediating, and suppressing inflammation could be helpful in developing new therapeutic approaches for these debilitating diseases. In this review, we present new information on three molecules with important roles in controlling inflammation: MALT1, Ariadne-2, and acetylcholine. We summarize our current state of knowledge of how these molecules function, and how they are involved in pathways of NF-κB activation or vagal nerve stimulation associated with inflammation.
不受控制的炎症是自身免疫性疾病和自身炎症综合征的一个特征,并且可能促进肿瘤发生。因此,鉴定调节引发、介导和抑制炎症的信号通路的分子,可能有助于开发针对这些使人衰弱疾病的新治疗方法。在本综述中,我们介绍了三种在控制炎症中起重要作用的分子的新信息:黏膜相关淋巴组织淋巴瘤易位蛋白1(MALT1)、阿里阿德涅蛋白2(Ariadne-2)和乙酰胆碱。我们总结了目前关于这些分子如何发挥作用,以及它们如何参与与炎症相关的核因子κB(NF-κB)激活途径或迷走神经刺激途径的知识状态。