Department of Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee.
Physiology (Bethesda). 2020 Mar 1;35(2):112-124. doi: 10.1152/physiol.00022.2019.
The innate immune system recognizes conserved pathogen-associated molecular patterns and produces inflammatory cytokines that direct downstream immune responses. The inappropriate localization of DNA within the cell cytosol or endosomal compartments indicates that a cell may either be infected by a DNA virus or bacterium, or has problems with its own nuclear integrity. This DNA is sensed by certain receptors that mediate cytokine production and, in some cases, initiate an inflammatory and lytic form of cell death called pyroptosis. Dysregulation of these DNA-sensing pathways is thought to contribute to autoimmune diseases and the development of cancer. In this review, we will discuss the DNA sensors Toll-like receptor 9 (TLR9), cyclic GMP-AMP synthase (cGAS), stimulator of interferon genes (STING), absent in melanoma 2 (AIM2), and interferon gamma-inducible 16 (IFI16), their ligands, and their physiological significance. We will also examine the less-well-understood DEAH- and DEAD-box helicases DHX9, DHX36, DDX41, and RNA polymerase III, each of which may play an important role in DNA-mediated innate immunity.
先天免疫系统识别保守的病原体相关分子模式,并产生炎症细胞因子,指导下游免疫反应。细胞内细胞质或内体区室中 DNA 的不当定位表明,细胞可能受到 DNA 病毒或细菌的感染,或者自身核完整性存在问题。某些受体可以感知这些 DNA,这些受体介导细胞因子的产生,并且在某些情况下,引发一种称为细胞焦亡的炎症和裂解形式的细胞死亡。这些 DNA 传感途径的失调被认为与自身免疫性疾病和癌症的发展有关。在这篇综述中,我们将讨论 DNA 传感器 Toll 样受体 9(TLR9)、环鸟苷酸-腺苷酸合酶(cGAS)、干扰素基因刺激因子(STING)、黑色素瘤缺失 2(AIM2)和干扰素 γ 诱导蛋白 16(IFI16),它们的配体及其生理意义。我们还将研究不太为人所知的 DEAH-和 DEAD-box 解旋酶 DHX9、DHX36、DDX41 和 RNA 聚合酶 III,它们中的每一种都可能在 DNA 介导的先天免疫中发挥重要作用。