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首页> 外文期刊>Nature Communications >DNA-PK deficiency potentiates cGAS-mediated antiviral innate immunity
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DNA-PK deficiency potentiates cGAS-mediated antiviral innate immunity

机译:DNA-PK缺乏症增强CGA介导的抗病毒天生免疫

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摘要

Upon sensing cytosolic DNA, the enzyme cGAS induces innate immune responses that underpin anti-microbial defenses and certain autoimmune diseases. Missense mutations of PRKDC encoding the DNA-dependent protein kinase (DNA-PK) catalytic subunit (DNA-PKcs) are associated with autoimmune diseases, yet how DNA-PK deficiency leads to increased immune responses remains poorly understood. In this study, we report that DNA-PK phosphorylates cGAS and suppresses its enzymatic activity. DNA-PK deficiency reduces cGAS phosphorylation and promotes antiviral innate immune responses, thereby potently restricting viral replication. Moreover, cells isolated from DNA-PKcs-deficient mice or patients carrying PRKDC missense mutations exhibit an inflammatory gene expression signature. This study provides a rational explanation for the autoimmunity of patients with missense mutations of PRKDC , and suggests that cGAS-mediated immune signaling is a potential target for therapeutic interventions.
机译:在感测细胞溶质DNA时,酶CGA诱导内先生免疫应答,使抗微生物防御和某些自身免疫疾病。编码DNA依赖性蛋白激酶(DNA-PK)催化亚基(DNA-PKCS)的PRKDC的畸形突变与自身免疫疾病有关,但DNA-PK缺乏如何导致增加的免疫应答仍然是较差的理解。在这项研究中,我们认为DNA-PK磷酸化CGA并抑制其酶活性。 DNA-PK缺乏减少CGA磷酸化并促进抗病毒先天免疫应答,从而易于限制病毒复制。此外,从DNA-PKCS缺陷小鼠中分离的细胞或携带PRKDC畸变突变的患者表现出炎症基因表达签名。本研究为PRKDC的畸形突变患者的自身免疫提供了合理的解释,并表明CGA介导的免疫信号传导是治疗干预措施的潜在目标。

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