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线粒体蛋白nmd在发育过程中调节脂质自噬和一般自噬。

Mitochondrial protein nmd regulates lipophagy and general autophagy during development.

作者信息

Wang Wei, Wang Xufeng, Zhou Xiaoqi, Jiang Lu, Shang Weina, Wang Liquan, Tong Chao

机构信息

Life Sciences Institute and State Key Laboratory of Transvascular Implantation Devices of the Second Affiliated Hospital of the Zhejiang University School of Medicine, Zhejiang University, Hangzhou, China.

MOE Key Laboratory for Biosystems Homeostasis & Protection and Innovation Center for Cell Signaling Network, Life Sciences Institute, Zhejiang University, Hangzhou, China.

出版信息

Autophagy. 2025 Jul 11:1-19. doi: 10.1080/15548627.2025.2522124.

Abstract

Lipophagy engulfs lipid droplets and delivers them to lysosomes for degradation. We found that lipophagy levels were low in most fly tissues, except for the prothoracic gland (PG) during larval development. Therefore, we performed a small-scale screening in the PG to identify regulators of lipophagy. We discovered that the loss of , a gene encoding a mitochondrial AAA-ATPase, led to developmental failure and reduced lipophagy in the PG. Further studies indicated that was not only required for lipophagy but also essential for general macroautophagy/autophagy in both PG and fat body tissues. Autophagy was induced but blocked at the autophagosome-lysosome fusion stage upon nmd reduction. Additionally, nmd interacted with mitochondrial protein import machinery, such as Tom20, Tom40, and the import cargo, such as Idh. Loss of decreased protein import into mitochondria. Similar to the loss of , reduction of Tom20 or Tom40 also resulted in reduced lipophagy in the PG. In adult flies, reducing expression in the eyes caused lipid droplet accumulation and severe degeneration during aging. Overexpression of bmm, a triglyceride lipase, reduced lipid droplets in the eye but did not rescue the eye degeneration caused by the reduction of .: ATAD1: ATPase family AAA domain containing 1; Atg8a: Autophagy-related 8a; Atg9: Autophagy-related 9; Atg14: Autophagy-related 14; Atg18a: Autophagy-related 18a; ATP: adenosine triphosphate; bmm: brummer; CtsL1: Cathepsin L1; Idh: isocitrate dehydrogenase (NADP+); Cis1: CItrinin Sensitive knockout; GFP: green fluorescent protein; LDs: lipid droplets; LIRs:LC3-interacting regions; Lsd-1: Lipid storage droplet-1; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; Marf: Mitochondrial assembly regulatory factor; Miga: Mitoguardin; Msp1: Mitochondrial Sorting of Proteins 1; nmd: no mitochondrial derivative; PG: prothoracic gland; phtm: phantom; PNPLA2/ATGL: patatin like domain 2, triacylglycerol lipase; RFP: red fluorescent protein; RNAi: RNA interference; Syx17: Syntaxin 17; TA: tail-anchored; TEM: transmission electron microscopy; TOMM: translocase of outermitochondrial membrane; Tom20: Translocase of outer membrane 20; Tom40: Translocase of outer membrane 40.

摘要

脂质自噬可吞噬脂滴并将其运送至溶酶体进行降解。我们发现,在大多数果蝇组织中脂质自噬水平较低,幼虫发育期间的前胸腺(PG)除外。因此,我们在前胸腺中进行了小规模筛选,以鉴定脂质自噬的调节因子。我们发现,编码线粒体AAA-ATP酶的基因缺失会导致发育失败并降低前胸腺中的脂质自噬水平。进一步研究表明,该基因不仅是脂质自噬所必需的,对于前胸腺和脂肪体组织中的一般巨自噬/自噬也是必不可少的。nmd减少后,自噬被诱导,但在自噬体-溶酶体融合阶段受阻。此外,nmd与线粒体蛋白导入机制相互作用,如Tom20、Tom40以及导入底物,如异柠檬酸脱氢酶(Idh)。该基因缺失会减少蛋白质向线粒体的导入。与该基因缺失相似,Tom20或Tom40减少也会导致前胸腺中脂质自噬水平降低。在成年果蝇中,降低眼睛中的该基因表达会导致脂滴积累以及衰老过程中的严重退化。甘油三酯脂肪酶bmm的过表达减少了眼睛中的脂滴,但无法挽救因该基因减少而导致的眼睛退化。:ATAD1:含ATP酶家族AAA结构域1;Atg8a:自噬相关蛋白8a;Atg9:自噬相关蛋白9;Atg14:自噬相关蛋白14;Atg18a:自噬相关蛋白18a;ATP:三磷酸腺苷;bmm:布勒默;CtsL1:组织蛋白酶L1;Idh:异柠檬酸脱氢酶(NADP+);Cis1:CItrinin敏感敲除;GFP:绿色荧光蛋白;LDs:脂滴;LIRs:LC3相互作用区域;Lsd-1:脂质储存液滴-1;MAP1LC3/LC3:微管相关蛋白1轻链3;Marf:线粒体组装调节因子;Miga:线粒体守护蛋白;Msp1:线粒体蛋白分选1;nmd:无线粒体衍生物;PG:前胸腺;phtm:幻影;PNPLA2/ATGL:类patatin结构域2,三酰甘油脂肪酶;RFP:红色荧光蛋白;RNAi:RNA干扰;Syx17: syntaxin 17;TA:尾锚定;TEM:透射电子显微镜;TOMM:线粒体外膜转位酶;Tom20:外膜转位酶20;Tom40:外膜转位酶40 。

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