Department of Immunology, Leiden University Medical Centre, Leiden, The Netherlands.
Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK.
EMBO J. 2022 Mar 15;41(6):e109760. doi: 10.15252/embj.2021109760. Epub 2022 Feb 14.
RNA editing by the adenosine deaminase ADAR1 prevents innate immune responses to endogenous RNAs. In ADAR1-deficient cells, unedited self RNAs form base-paired structures that resemble viral RNAs and inadvertently activate the cytosolic RIG-I-like receptor (RLR) MDA5, leading to an antiviral type I interferon (IFN) response. Mutations in ADAR1 cause Aicardi-Goutières Syndrome (AGS), an autoinflammatory syndrome characterized by chronic type I IFN production. Conversely, ADAR1 loss and the consequent type I IFN production restricts tumor growth and potentiates the activity of some chemotherapeutics. Here, we show that another RIG-I-like receptor, LGP2, also has an essential role in the induction of a type I IFN response in ADAR1-deficient human cells. This requires the canonical function of LGP2 as an RNA sensor and facilitator of MDA5-dependent signaling. Furthermore, we show that the sensitivity of tumor cells to ADAR1 loss requires LGP2 expression. Finally, type I IFN induction in tumor cells depleted of ADAR1 and treated with some chemotherapeutics fully depends on LGP2 expression. These findings highlight a central role for LGP2 in self RNA sensing with important clinical implications.
RNA 编辑由腺苷脱氨酶 ADAR1 完成,可防止内源性 RNA 引发固有免疫反应。在 ADAR1 缺陷细胞中,未经编辑的自身 RNA 形成碱基配对结构,类似于病毒 RNA,从而错误地激活细胞质 RIG-I 样受体 (RLR) MDA5,导致抗病毒 I 型干扰素 (IFN) 反应。ADAR1 中的突变导致 Aicardi-Goutières 综合征 (AGS),这是一种以慢性 I 型 IFN 产生为特征的自身炎症综合征。相反,ADAR1 的缺失和随之而来的 I 型 IFN 产生限制了肿瘤生长并增强了某些化疗药物的活性。在这里,我们表明另一种 RIG-I 样受体 LGP2 在 ADAR1 缺陷的人类细胞中诱导 I 型 IFN 反应中也具有重要作用。这需要 LGP2 作为 RNA 传感器和 MDA5 依赖性信号转导的辅助因子的典型功能。此外,我们表明肿瘤细胞对 ADAR1 缺失的敏感性需要 LGP2 表达。最后,用某些化疗药物处理 ADAR1 耗尽的肿瘤细胞后诱导 I 型 IFN 的完全依赖于 LGP2 的表达。这些发现突出了 LGP2 在自身 RNA 感应中的核心作用,具有重要的临床意义。