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ATG16L1 变异体在非经典自噬依赖性中的作用:对尿路上皮囊泡运输和尿路致病性大肠杆菌持续存在的影响。

A non-canonical autophagy-dependent role of the ATG16L1 variant in urothelial vesicular trafficking and uropathogenic Escherichia coli persistence.

机构信息

a Department of Obstetrics and Gynecology , Washington University School of Medicine , St. Louis , MO , USA.

b Pathology and Immunology , Washington University School of Medicine , St. Louis , MO , USA.

出版信息

Autophagy. 2019 Mar;15(3):527-542. doi: 10.1080/15548627.2018.1535290. Epub 2018 Nov 8.

Abstract

50% of Caucasians carry a Thr300Ala variant (T300A) in the protein encoded by the macroautophagy/autophagy gene ATG16L1. Here, we show that the T300A variant confers protection against urinary tract infections (UTIs), the most common infectious disease in women. Using knockin mice carrying the human T300A variant, we show that the variant limits the UTI-causing bacteria, uropathogenic Escherichia coli (UPEC), from establishing persistent intracellular reservoirs, which can seed UTI recurrence. This phenotype is recapitulated in mice lacking Atg16l1 or Atg7 exclusively in the urothelium. We further show that mice with the T300A variant exhibit urothelial cellular abnormalities, including vesicular congestion and aberrant accumulation of UPK (uroplakin) proteins. Importantly, presence of the T300A variant in humans is associated with similar urothelial architectural abnormalities, indicating an evolutionarily conserved impact. Mechanistically, we show that the reduced bacterial persistence is independent of basal autophagic flux or proinflammatory cytokine responses and does not involve Atg14 or Epg5. However, the T300A variant is associated with increased expression of the small GTPase Rab33b; RAB33B interacts with ATG16L1, as well as other secretory RABs, RAB27B and RAB11A, important for UPEC exocytosis from the urothelium. Finally, inhibition of secretory RABs in bladder epithelial cells increases intracellular UPEC load. Together, our results reveal that UPEC selectively utilize genes important for autophagosome formation to persist in the urothelium, and that the presence of the T300A variant in ATG16L1 is associated with changes in urothelial vesicle trafficking, which disrupts the ability of UPEC to persist, thereby limiting the risk of recurrent UTIs. Abbreviations: 3-PEHPC: 3-pyridinyl ethylidene hydroxyl phosphonocarboxylate; ATG: autophagy; ATG16L1: autophagy related 16 like 1; BECs: bladder epithelial cells; dpi: days post infection; hpi: hours post infection; IF: immunofluorescence; IL1B: interleukin 1 beta; IL6: interleukin 6; MAP1LC3B/LC3B: microtubule-associated protein 1 light chain 3 beta; MVB: multivesicular bodies; T300A: Thr300Ala; TNF: tumor necrosis factor; QIR(s): quiescent intracellular reservoir(s); siRNA: short interfering RNA; UPEC: uropathogenic Escherichia coli; UTI(s): urinary tract infection(s); TEM: transmission electron microscopy; WT: wild type.

摘要

50%的白种人携带由宏自噬/自噬基因 ATG16L1 编码的蛋白质中的 Thr300Ala 变体 (T300A)。在这里,我们表明该变体可提供针对尿路感染 (UTI) 的保护,UTI 是女性最常见的传染病。使用携带人类 T300A 变体的基因敲入小鼠,我们表明该变体限制了引起 UTI 的细菌,尿路致病性大肠杆菌 (UPEC) 建立持续的细胞内储库,这些储库可引发 UTI 复发。这种表型在 urothelium 中特异性缺乏 Atg16l1 或 Atg7 的小鼠中得到重现。我们进一步表明,携带 T300A 变体的小鼠表现出尿路上皮细胞异常,包括囊泡充血和 UPK(uroplakin)蛋白的异常积累。重要的是,人类存在 T300A 变体与类似的尿路上皮结构异常相关,表明存在进化保守的影响。在机制上,我们表明细菌持续存在的减少与基础自噬通量或促炎细胞因子反应无关,也不涉及 Atg14 或 Epg5。然而,T300A 变体与小 GTPase Rab33b 的表达增加有关;RAB33B 与 ATG16L1 以及其他分泌性 RAB(RAB27B 和 RAB11A)相互作用,对于 UPEC 从尿路上皮的胞吐作用很重要。最后,抑制膀胱上皮细胞中的分泌性 RAB 会增加细胞内 UPEC 负荷。总之,我们的结果表明,UPEC 选择性地利用自噬体形成的重要基因在尿路上皮中持续存在,而 ATG16L1 中的 T300A 变体与尿路上皮囊泡运输的变化有关,这破坏了 UPEC 持续存在的能力,从而限制了复发性 UTI 的风险。缩写:3-PEHPC:3-吡啶基乙基亚甲基羟膦酸酯;ATG:自噬;ATG16L1:自噬相关 16 样 1;BECs:膀胱上皮细胞;dpi:感染后天数;hpi:感染后小时数;IF:免疫荧光;IL1B:白细胞介素 1 beta;IL6:白细胞介素 6;MAP1LC3B/LC3B:微管相关蛋白 1 轻链 3 beta;MVB:多泡体;T300A:Thr300Ala;TNF:肿瘤坏死因子;QIR(s):静止细胞内储库(s);siRNA:短发夹 RNA;UPEC:尿路致病性大肠杆菌;UTI(s):尿路感染(s);TEM:透射电子显微镜;WT:野生型。

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