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PDZD8 缺陷型小鼠由于大脑中的脂质代谢紊乱,表现出与情绪、认知和适应能力相关的行为异常。

PDZD8-deficient mice manifest behavioral abnormalities related to emotion, cognition, and adaptation due to dyslipidemia in the brain.

机构信息

Department of Molecular Biology, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, Aichi, Japan.

Division of Systems Medical Science, Center for Medical Science, Fujita Health University, Toyoake, Aichi, Japan.

出版信息

Mol Brain. 2023 Jan 19;16(1):11. doi: 10.1186/s13041-023-01002-4.

Abstract

Although dyslipidemia in the brain has been implicated in neurodegenerative disorders, the molecular mechanisms underlying its pathogenesis have been largely unclear. PDZD8 is a lipid transfer protein and mice deficient in PDZD8 (PDZD8-KO mice) manifest abnormal accumulation of cholesteryl esters (CEs) in the brain due to impaired lipophagy, the degradation system of lipid droplets. Here we show the detailed mechanism of PDZD8-dependent lipophagy. PDZD8 transports cholesterol to lipid droplets (LDs), and eventually promotes fusion of LDs and lysosomes. In addition, PDZD8-KO mice exhibit growth retardation, hyperactivity, reduced anxiety and fear, increased sensorimotor gating, and impaired cued fear conditioned memory and working memory. These results indicate that abnormal CE accumulation in the brain caused by PDZD8 deficiency affects emotion, cognition and adaptive behavior, and that PDZD8 plays an important role in the maintenance of brain function through lipid metabolism.

摘要

尽管脑内脂质代谢紊乱与神经退行性疾病有关,但该病的发病机制在很大程度上仍不清楚。PDZD8 是一种脂转移蛋白,PDZD8 缺陷(PDZD8-KO 小鼠)的小鼠由于脂噬(脂质滴的降解系统)受损,脑内胆固醇酯(CEs)异常积聚。本文展示了 PDZD8 依赖的脂噬的详细机制。PDZD8 将胆固醇转运到脂滴(LDs),最终促进 LDs 与溶酶体融合。此外,PDZD8-KO 小鼠表现出生长迟缓、多动、焦虑和恐惧减少、感觉运动门控增加以及条件恐惧记忆和工作记忆受损。这些结果表明,PDZD8 缺乏导致脑内 CE 异常积聚,影响情绪、认知和适应行为,PDZD8 通过脂质代谢在维持脑功能方面发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5687/9854033/25ac74f5d122/13041_2023_1002_Fig1_HTML.jpg

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