在单核细胞增生乳杆菌感染期间,RNF144A通过靶向BECN1降解来抑制自噬。

Bo Yang, Mengyang Shen, Chen Lu, Yi Wang, Xin Zhao, Qunmei Zhang, Xiao Qin, Jinyong Pei, Hui Wang, Jie Wang
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引用次数: 0

摘要

单核增生李斯特菌(Listeria monocytogenes, Lm)在实验室中被广泛用作研究革兰氏阳性胞内细菌的发病机制和宿主防御的感染模型。巨噬(以下简称“自噬”)在宿主防御病原体(如细菌、病毒和寄生虫)中起着重要作用。BECN1在自噬的启动中起着关键作用,越来越多的证据表明,BECN1的翻译后修饰为自噬调控提供了多种策略。在这项研究中,我们证明了RING1-IBR-RING2 (RBR)家族成员RNF144A (ring finger protein 144A)在Lm感染诱导下,以自噬依赖但不依赖于sting1的模式促进Lm感染。小鼠rnf144a缺陷通过抑制先天免疫反应保护小鼠免受Lm感染。有趣的是,RNF144A降低了lm诱导的自噬体积累。机制研究表明,RNF144A与BECN1相互作用,促进其与k48相关的泛素化,导致BECN1随后依赖蛋白酶体降解,减少自噬体积累。进一步研究表明,RNF144A促进了BECN1在K117和K427位点的泛素化,这两个泛素化位点对于BECN1在自噬和Lm感染中的作用至关重要。因此,我们的发现提示了细胞内细菌感染和自噬的新调节因子,这可能有助于我们理解宿主通过自噬防御细胞内细菌感染。缩写:ATG3:自噬相关3;ATG5:自噬相关5;ATG7:自噬相关7;ATG10:自噬相关10;ATG12:自噬相关12;ATG16L1:自噬相关16样1;Baf A1:巴霉素A1;BECN1: beclin 1;BMDC:骨髓源性树突状细胞;BMDM:骨髓源性巨噬细胞;cfu:菌落形成单位;CHX:环己酰亚胺;CQ:氯喹;CXCL10/IP-10: C-X-C基序趋化因子配体10;厄尔平衡盐溶液;ELISA:酶联免疫吸附法;IFIT1/ISG56:干扰素诱导蛋白与四肽重复1;IFNB/IFN-β:干扰素β;IL6:白细胞介素6;IRF3,干扰素调节因子3;Lm:单核增生乳杆菌;MAP1LC3/LC3:微管相关蛋白1轻链3;MEF:小鼠胚胎成纤维细胞;MOI:感染多重性;PLA:近端结扎试验;PMA:肉豆蔻酸酯佛博尔酯;PMA-THP1, pma分化的THP1;PMs:腹膜巨噬细胞;PTMs:翻译后修饰;RBR: RING1-IBR-RING2;RNF144A:无名指蛋白144A;干扰素应答刺激因子STING1;TBK1, TANK结合激酶1;TNF/TNF-α:肿瘤坏死因子。
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RNF144A inhibits autophagy by targeting BECN1 for degradation during L. monocytogenes infection.

Listeria monocytogenes (L. monocytogenes, Lm) is widely used in the laboratory as an infection model for the research on pathogenesis and host defense against gram-positive intracellular bacteria. Macroautophagy (called simply "autophagy" hereafter), is important in the host defense against pathogens, such as bacteria, viruses, and parasites. BECN1 plays a pivotal role in the initiation of autophagy and accumulating evidence indicates that post-translational modifications of BECN1 provide multiple strategies for autophagy regulation. In this study, we demonstrated that the RING1-IBR-RING2 (RBR) family member RNF144A (ring finger protein 144A), which was induced by Lm infection, promoted Lm infection in an autophagy-dependent but STING1-independent pattern. rnf144a deficiency in mice protected mice from Lm infection with inhibited innate immune responses. Interestingly, RNF144A decreased Lm-induced autophagosome accumulation. Mechanistic investigation indicated that RNF144A interacted with BECN1 and promoted its K48-linked ubiquitination, leading to the subsequent proteasome-dependent degradation of BECN1 and reduced autophagosome accumulation. Further study demonstrated that RNF144A promoted the ubiquitination of BECN1 at K117 and K427, and these two ubiquitination sites were essential to the role of BECN1 in autophagy and Lm infection. Thus, our findings suggested a new regulator in intracellular bacterial infection and autophagy, which may contribute to our understanding of host defense against intracellular bacterial infection via autophagy.Abbreviations: ATG3: autophagy related 3; ATG5: autophagy related 5; ATG7: autophagy related 7; ATG10: autophagy related 10; ATG12: autophagy related 12; ATG16L1: autophagy related 16 like 1; Baf A1: bafilomycin A1; BECN1: beclin 1; BMDC: bone marrow-derived dendritic cell; BMDM: bone marrow-derived macrophage; CFUs: colony-forming units; CHX: cycloheximide; CQ: chloroquine; CXCL10/IP-10: C-X-C motif chemokine ligand 10; EBSS: Earle's balanced salt solution; ELISA: enzyme-linked immunosorbent assay; IFIT1/ISG56: interferon induced protein with tetratricopeptide repeats 1; IFNB/IFN-β: interferon beta; IL6: interleukin 6; IRF3, interferon regulatory factor 3; Lm: L. monocytogenes; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; MEF: mouse embryonic fibroblast; MOI: multiplicity of infection; PLA: proximity ligation assay; PMA: phorbol myristate acetate; PMA-THP1, PMA-differentiated THP1; PMs: peritoneal macrophages; PTMs: posttranslational modifications; RBR: RING1-IBR-RING2; RNF144A: ring finger protein 144A; STING1, stimulator of interferon response cGAMP interactor 1; TBK1, TANK binding kinase 1; TNF/TNF-α: tumor necrosis factor.

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