TFEB and TFE3 regulate STING1-dependent immune responses by controlling type I interferon signaling.

Pablo J Tapia, José A Martina, Pablo S Contreras, Akriti Prashar, Eutteum Jeong, Dominic De Nardo, Rosa Puertollano
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Abstract

STING1 is an essential component of the innate immune defense against a wide variety of pathogens. Whereas induction of type I interferon (IFN) responses is one of the best-defined functions of STING1, our transcriptomic analysis revealed IFN-independent activities of STING1 in macrophages, including transcriptional upregulation of numerous lysosomal and autophagic genes. This upregulation was mediated by the STING1-induced activation of the transcription factors TFEB and TFE3, and led to increased autophagy, lysosomal biogenesis, and lysosomal acidification. TFEB and TFE3 also modulated IFN-dependent STING1 signaling by controlling IRF3 activation. IFN production and cell death were increased in TFEB- and TFE3-depleted iBMDMs. Conversely, TFEB overexpression led to reduced IRF3 activation and an almost complete inhibition of IFN synthesis and secretion, resulting in decreased CASP3 activation and increased cell survival. Our study reveals a key role of TFEB and TFE3 as regulators of STING1-mediated innate antiviral immunity.Abbreviation: ACOD1/IRG1, aconitate decarboxylase 1; cGAMP, cyclic guanosine monophosphate-adenosine monophosphate; CGAS, cyclic GMP-AMP synthase; DMXAA, 5,6-dimethylxanthenone-4-acetic acid; EIF4EBP1, eukaryotic translation initiation factor 4E binding protein 1; GABARAP, GABA type A receptor-associated protein; HSV-1, herpes simplex virus type; iBMDMs, immortalized bone marrow-derived macrophages; IFN, type I interferon; IFNB, interferon beta; IKBKE, inhibitor of nuclear factor kappa B kinase subunit epsilon; IRF3, interferon regulatory factor 3; LAMP1, lysosomal associated membrane protein 1; LAMP2, lysosomal associated membrane protein 2; MTORC1, mechanistic target of rapamycin kinase complex 1; RPS6, ribosomal protein S6; STING1, stimulator of interferon response cGAMP interactor 1; TBK1, TANK binding kinase 1; TFE3, transcription factor binding to IGHM enhancer 3; TFEB, transcription factor EB.

TFEB和TFE3通过控制I型干扰素信号传导调节sting - 1依赖性免疫应答。
STING1是先天免疫防御多种病原体的重要组成部分。虽然诱导I型干扰素(IFN)应答是STING1最明确的功能之一,但我们的转录组学分析显示,巨噬细胞中STING1的IFN独立活性,包括许多溶酶体和自噬基因的转录上调。这种上调是由sting1诱导的转录因子TFEB和TFE3的激活介导的,并导致自噬、溶酶体生物发生和溶酶体酸化增加。TFEB和TFE3也通过控制IRF3的激活来调节ifn依赖性的STING1信号。在TFEB-和tfe3缺失的iBMDMs中,IFN的产生和细胞死亡增加。相反,TFEB过表达导致IRF3激活降低,IFN合成和分泌几乎完全抑制,导致CASP3激活降低,细胞存活率增加。我们的研究揭示了TFEB和TFE3作为sting 1介导的先天抗病毒免疫的调节因子的关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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