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cGAS 有助于检测细胞外环二核苷酸以激活先天免疫。

cGAS facilitates sensing of extracellular cyclic dinucleotides to activate innate immunity.

机构信息

Department of Immunology, Max Planck Institute for Infection Biology, Berlin, Germany.

Shanghai Key Laboratory of Tuberculosis, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.

出版信息

EMBO Rep. 2019 Apr;20(4). doi: 10.15252/embr.201846293. Epub 2019 Mar 14.

Abstract

Cyclic dinucleotides (CDNs) are important second messenger molecules in prokaryotes and eukaryotes. Within host cells, cytosolic CDNs are detected by STING and alert the host by activating innate immunity characterized by type I interferon (IFN) responses. Extracellular bacteria and dying cells can release CDNs, but sensing of extracellular CDNs (eCDNs) by mammalian cells remains elusive. Here, we report that endocytosis facilitates internalization of eCDNs. The DNA sensor cGAS facilitates sensing of endocytosed CDNs, their perinuclear accumulation, and subsequent STING-dependent release of type I IFN Internalized CDNs bind cGAS directly, leading to its dimerization, and the formation of a cGAS/STING complex, which may activate downstream signaling. Thus, eCDNs comprise microbe- and danger-associated molecular patterns that contribute to host-microbe crosstalk during health and disease.

摘要

环二核苷酸(CDNs)是原核生物和真核生物中重要的第二信使分子。在宿主细胞内,细胞质 CDNs 被 STING 检测到,并通过激活以 I 型干扰素(IFN)反应为特征的固有免疫来提醒宿主。胞外细菌和死亡细胞可以释放 CDNs,但哺乳动物细胞对胞外 CDNs(eCDNs)的感应仍然难以捉摸。在这里,我们报告内吞作用促进了 eCDNs 的内化。DNA 传感器 cGAS 有助于感应内吞的 CDNs,它们在核周的积累,以及随后 STING 依赖性释放 I 型 IFN。内吞的 CDNs 直接与 cGAS 结合,导致其二聚化,并形成 cGAS/STING 复合物,这可能激活下游信号。因此,eCDNs 包括微生物和危险相关的分子模式,它们在健康和疾病期间有助于宿主-微生物的串扰。

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