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巨大多巴胺受体蛋白在肝内细胞酒精后高尔基体内膜修复中的作用

Giantin Is Required for Post-Alcohol Recovery of Golgi in Liver Cells.

机构信息

Department of Internal Medicine and VA-Nebraska-Western Iowa Health Care System, Omaha, NE 68105, USA.

Department of Biochemistry and Molecular Biology, College of Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USA.

出版信息

Biomolecules. 2018 Nov 16;8(4):150. doi: 10.3390/biom8040150.

Abstract

In hepatocytes and alcohol-metabolizing cultured cells, Golgi undergoes ethanol (EtOH)-induced disorganization. Perinuclear and organized Golgi is important in liver homeostasis, but how the Golgi remains intact is unknown. Work from our laboratories showed that EtOH-altered cellular function could be reversed after alcohol removal; we wanted to determine whether this recovery would apply to Golgi. We used alcohol-metabolizing HepG2 (VA-13) cells (cultured with or without EtOH for 72 h) and rat hepatocytes (control and EtOH-fed (Lieber⁻DeCarli diet)). For recovery, EtOH was removed and replenished with control medium (48 h for VA-13 cells) or control diet (10 days for rats). Results: EtOH-induced Golgi disassembly was associated with de-dimerization of the largest Golgi matrix protein giantin, along with impaired transport of selected hepatic proteins. After recovery from EtOH, Golgi regained their compact structure, and alterations in giantin and protein transport were restored. In VA-13 cells, when we knocked down giantin, Rab6a GTPase or non-muscle myosin IIB, minimal changes were observed in control conditions, but post-EtOH recovery was impaired. Conclusions: These data provide a link between Golgi organization and plasma membrane protein expression and identify several proteins whose expression is important to maintain Golgi structure during the recovery phase after EtOH administration.

摘要

在肝细胞和酒精代谢培养细胞中,高尔基体会发生乙醇(EtOH)诱导的结构紊乱。核周和有组织的高尔基复合体对于肝脏的稳态很重要,但高尔基复合体如何保持完整尚不清楚。我们实验室的工作表明,在去除酒精后,酒精改变的细胞功能可以逆转;我们想确定这种恢复是否适用于高尔基复合体。我们使用酒精代谢的 HepG2(VA-13)细胞(用或不用 EtOH 培养 72 小时)和大鼠肝细胞(对照和 EtOH 喂养(Lieber⁻DeCarli 饮食))。对于恢复,去除 EtOH 并用对照培养基(VA-13 细胞 48 小时)或对照饮食(大鼠 10 天)补充。结果:EtOH 诱导的高尔基解体与最大的高尔基基质蛋白 giantin 的解二聚化以及选定的肝蛋白的运输受损有关。在 EtOH 恢复后,高尔基复合体恢复了其紧凑的结构,giantin 和蛋白运输的改变得到了恢复。在 VA-13 细胞中,当我们敲低 giantin、Rab6a GTPase 或非肌肉肌球蛋白 IIB 时,在对照条件下观察到的变化很小,但 EtOH 恢复后的变化受损。结论:这些数据将高尔基复合体的组织与质膜蛋白表达联系起来,并确定了几种表达蛋白,这些蛋白对于在 EtOH 给药后的恢复阶段维持高尔基复合体结构很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7733/6316505/08fb402bc10d/biomolecules-08-00150-g001.jpg

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