Aster-B coordinates with Arf1 to regulate mitochondrial cholesterol transport

被引:27
作者
Andersen, John-Paul [1 ]
Zhang, Jun [1 ]
Sun, Haoran [2 ]
Liu, Xuyun [1 ,3 ]
Liu, Jiankang [3 ]
Nie, Jia [1 ]
Shi, Yuguang [1 ,2 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Sam & Ann Barshop Inst Longev & Aging Studies, Dept Pharmacol, Texas Res Pk Campus MC 7755,15355 Lambda Dr, San Antonio, TX 78245 USA
[2] Nanjing Med Univ, Dept Biochem & Mol Biol, Nanjing, Peoples R China
[3] Xi An Jiao Tong Univ, Ctr Mitochondrial Biol & Med, Sch Life Sci & Technol, Key Lab Biomed,Informat Engn,Minist Educ, Xian, Shaanxi, Peoples R China
基金
美国国家卫生研究院;
关键词
GRAMD1b; Cholesterol transport; Mitochondria; Arf1; Fatty acids;
D O I
10.1016/j.molmet.2020.101055
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Cholesterol plays a pivotal role in mitochondrial steroidogenesis, membrane structure, and respiration. Mitochondrial membranes are intrinsically low in cholesterol content and therefore must be replenished with cholesterol from other subcellular membranes. However, the molecular mechanisms underlying mitochondrial cholesterol transport remains poorly understood. The Aster-B gene encodes a cholesterol binding protein recently implicated in cholesterol trafficking from the plasma membrane to the endoplasmic reticulum (ER). In this study, we investigated the function and underlying mechanism of Aster-B in mediating mitochondria! cholesterol transport. Methods: CRISPR/Cas9 gene editing was carried out to generate cell lines deficient in Aster-B expression. The effect of Aster-B deficiency on mitochondria! cholesterol transport was examined by both confocal imaging analysis and biochemical assays. Deletion mutational analysis was also carried out to identify the function of a putative mitochondria! targeting sequence (MTS) at the N-terminus of Aster-B for its role in targeting Aster-B to mitochondria and in mediating mitochondrial cholesterol trafficking. Results: Ablation of Aster-B impaired cholesterol transport from the ER to mitochondria, leading to a significant decrease in mitochondrial cholesterol content. Aster-B is also required for mitochondria! transport of fatty acids derived from hydrolysis of cholesterol esters. A putative MTS at the N-terminus of Aster-B mediates the mitochondria! cholesterol uptake. Deletion of the MTS or ablation of Arfl GTPase which is required for mitochondria! translocation of ER proteins prevented mitochondria! cholesterol transport, leading to mitochondria! dysfunction. Conclusions: We identified Aster-B as a key regulator of cholesterol transport from the ER to mitochondria. Aster-B also coordinates mitochondrial cholesterol trafficking with uptake of fatty acids derived from cholesterol esters, implicating the Aster-B protein as a novel regulator of steroidogenesis. Published by Elsevier GmbH.
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页数:13
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