a Department of Immunology , School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology , Wuhan , China.
b Department of Surgery, Tongji Hospital , Huazhong University of Science and Technology , Wuhan , China.
Autophagy. 2019 Jun;15(6):960-975. doi: 10.1080/15548627.2019.1569916. Epub 2019 Jan 29.
Macroautophagy/autophagy is a conserved ubiquitous pathway that performs diverse roles in health and disease. Although many key, widely expressed proteins that regulate autophagosome formation followed by lysosomal fusion have been identified, the possibilities of cell-specific elements that contribute to the autophagy fusion machinery have not been explored. Here we show that a macrophage-specific isoform of the vacuolar ATPase protein ATP6V0D2/subunit d2 is dispensable for lysosome acidification, but promotes the completion of autophagy via promotion of autophagosome-lysosome fusion through its interaction with STX17 and VAMP8. Atp6v0d2-deficient macrophages have augmented mitochondrial damage, enhanced inflammasome activation and reduced clearance of Salmonella typhimurium. The susceptibility of atp6v0d2 knockout mice to DSS-induced colitis and Salmonella typhimurium-induced death, highlights the in vivo significance of ATP6V0D2-mediated autophagosome-lysosome fusion. Together, our data identify ATP6V0D2 as a key component of macrophage-specific autophagosome-lysosome fusion machinery maintaining macrophage organelle homeostasis and, in turn, limiting both inflammation and bacterial infection. Abbreviations: ACTB/β-actin: actin, beta; ATG14: autophagy related 14; ATG16L1: autophagy related 16-like 1 (S. cerevisiae); ATP6V0D1/2: ATPase, H+ transporting, lysosomal V0 subunit D1/2; AIM2: absent in melanoma 2; BMDM: bone marrow-derived macrophage; CASP1: caspase 1; CGD: chronic granulomatous disease; CSF1/M-CSF: colony stimulating factor 1 (macrophage); CTSB: cathepsin B; DSS: dextran sodium sulfate; IL1B: interleukin 1 beta; IL6: interleukin 6; IRGM: immunity-related GTPase family M member; KO: knockout; LAMP1: lysosomal-associated membrane protein 1; LC3: microtubule-associated protein 1 light chain 3; LPS: lipo-polysaccaride; NLRP3: NLR family, pyrin domain containing 3; PYCARD/ASC: PYD and CARD domain containing; SNARE: soluble N-ethylmaleimide-sensitive factor attachment protein receptor; SNAP29: synaptosomal-associated protein 29; SQSTM1/p62: sequestosome 1; STX17: syntaxin 17; TLR: toll-like receptor; TNF: tumor necrosis factor ; TOMM20: translocase of outer mitochondrial membrane 20; ULK1: unc-51 like kinase 1; VAMP8: vesicle-associated membrane protein 8; WT: wild type; 3-MA: 3-methyladenine.
自噬是一种保守的普遍存在的途径,在健康和疾病中发挥着多种作用。尽管已经鉴定出许多广泛表达的调节自噬体形成随后溶酶体融合的关键蛋白,但尚未探索有助于自噬融合机制的细胞特异性元件的可能性。在这里,我们显示巨噬细胞特异性空泡型 ATP 酶蛋白 ATP6V0D2/亚基 d2 的同工型对于溶酶体酸化不是必需的,但是通过与 STX17 和 VAMP8 的相互作用促进自噬体-溶酶体融合,从而促进自噬的完成。Atp6v0d2 缺陷型巨噬细胞中线粒体损伤增加,炎症小体激活增强,鼠伤寒沙门氏菌清除减少。Atp6v0d2 敲除小鼠对 DSS 诱导的结肠炎和鼠伤寒沙门氏菌诱导的死亡的易感性,突出了 ATP6V0D2 介导的自噬体-溶酶体融合在体内的重要性。总之,我们的数据将 ATP6V0D2 鉴定为维持巨噬细胞细胞器稳态的巨噬细胞特异性自噬体-溶酶体融合机制的关键组成部分,从而限制炎症和细菌感染。缩写:ACTB/β-肌动蛋白:肌动蛋白,β;ATG14:自噬相关 14;ATG16L1:自噬相关 16 样 1(酿酒酵母);ATP6V0D1/2:ATPase,H+运输,溶酶体 V0 亚基 D1/2;AIM2:黑色素瘤 2 缺失;BMDM:骨髓来源的巨噬细胞;CASP1:半胱天冬酶 1;CGD:慢性肉芽肿病;CSF1/M-CSF:集落刺激因子 1(巨噬细胞);CTSB:组织蛋白酶 B;DSS:葡聚糖硫酸钠;IL1B:白细胞介素 1β;IL6:白细胞介素 6;IRGM:免疫相关 GTP 酶家族 M 成员;KO:敲除;LAMP1:溶酶体相关膜蛋白 1;LC3:微管相关蛋白 1 轻链 3;LPS:脂多糖;NLRP3:NLR 家族,包含 pyrin 结构域的 3;PYCARD/ASC:包含 PYD 和 CARD 结构域的;SNARE:可溶性 N-乙基马来酰亚胺敏感因子附着蛋白受体;SNAP29:突触相关蛋白 29;SQSTM1/p62:自噬体 1;STX17:突触融合蛋白 17;TLR: toll 样受体;TNF:肿瘤坏死因子;TOMM20:外线粒体膜转运蛋白 20;ULK1:UNC-51 样激酶 1;VAMP8:囊泡相关膜蛋白 8;WT:野生型;3-MA:3-甲基腺嘌呤。