1] Program in Innate Immunity, Division of Infectious Diseases and Immunology, Department of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA. [2].
1] Howard Hughes Medical Institute, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA. [2].
Nat Rev Immunol. 2014 Jun;14(6):361-76. doi: 10.1038/nri3682.
Innate immune responses combat infectious microorganisms by inducing inflammatory responses, antimicrobial pathways and adaptive immunity. Multiple genes within each of these functional categories are coordinately and temporally regulated in response to distinct external stimuli. The substantial potential of these responses to drive pathological inflammation and tissue damage highlights the need for rigorous control of these responses. Although transcriptional control of inflammatory gene expression has been studied extensively, the importance of post-transcriptional regulation of these processes is less well defined. In this Review, we discuss the regulatory mechanisms that occur at the level of mRNA splicing, mRNA polyadenylation, mRNA stability and protein translation, and that have instrumental roles in controlling both the magnitude and duration of the inflammatory response.
先天免疫反应通过诱导炎症反应、抗菌途径和适应性免疫来对抗感染性微生物。这些功能类别中的多个基因会针对不同的外部刺激进行协调和时间上的调节。这些反应具有驱动病理性炎症和组织损伤的巨大潜力,这凸显了严格控制这些反应的必要性。尽管转录控制炎症基因表达已得到广泛研究,但这些过程的转录后调控的重要性还不太明确。在这篇综述中,我们讨论了在 mRNA 剪接、mRNA 多聚腺苷酸化、mRNA 稳定性和蛋白质翻译水平上发生的调节机制,这些机制在控制炎症反应的幅度和持续时间方面发挥了重要作用。