Zhu Qifan, Kanneganti Thirumala-Devi
Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105; and.
Integrated Biomedical Sciences Program, University of Tennessee Health Science Center, Memphis, TN 38163.
J Immunol. 2017 Jun 1;198(11):4210-4215. doi: 10.4049/jimmunol.1700352. Epub 2017 May 3.
Interleukin-18 and IL-1β, which are cytokines of the IL-1 family, are synthesized as precursor proteins and activated by the inflammasome via proteolytic processing. IL-1β is only induced in response to inflammatory stimuli, but IL-18 is constitutively expressed. However, how IL-18 and IL-1β expression is regulated by different inflammatory signals remains poorly studied. In this study, we found that IL-18 and IL-1β are differentially regulated. Despite being constitutively expressed, IL-18 expression was increased and sustained after stimulation of TLRs. In contrast, IL-1β was induced but not sustained after chronic treatment. Furthermore, type I IFN signaling was essential for induction of IL-18 and macrophages lacking type I IFN signaling were impaired in their ability to promote IL-18 induction. Thus, our findings reveal a fundamental difference in IL-18 and IL-1β regulation and uncover novel mechanisms that are relevant to the inflammatory settings where these proinflammatory cytokines play a critical role.
白细胞介素-18(IL-18)和IL-1β属于IL-1家族细胞因子,以前体蛋白形式合成,并通过炎性小体经蛋白水解加工而激活。IL-1β仅在炎症刺激下诱导产生,而IL-18组成性表达。然而,IL-18和IL-1β的表达如何受不同炎症信号调控仍研究不足。在本研究中,我们发现IL-18和IL-1β受到不同的调控。尽管IL-18组成性表达,但在Toll样受体(TLR)刺激后其表达增加并持续存在。相反,慢性处理后IL-1β被诱导但未持续。此外,I型干扰素信号对于IL-18的诱导至关重要,缺乏I型干扰素信号的巨噬细胞促进IL-18诱导的能力受损。因此,我们的研究结果揭示了IL-18和IL-1β调控的根本差异,并揭示了与这些促炎细胞因子发挥关键作用的炎症环境相关的新机制。