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细胞内胆固醇转运的新机制:氧化固醇结合蛋白和膜接触位点。

Novel mechanisms of intracellular cholesterol transport: oxysterol-binding proteins and membrane contact sites.

机构信息

School of Biotechnology and Biomolecular Sciences, The University of New South Wales, Sydney, NSW 2052, Australia.

School of Biotechnology and Biomolecular Sciences, The University of New South Wales, Sydney, NSW 2052, Australia.

出版信息

Curr Opin Cell Biol. 2015 Aug;35:37-42. doi: 10.1016/j.ceb.2015.04.002. Epub 2015 Apr 29.

Abstract

Cholesterol is an essential membrane constituent, and also plays a key role in cell signalling. Within a cell, how cholesterol is transported and how its heterogeneous distribution is maintained are poorly understood. Recent advances have identified novel pathways and regulators of cholesterol trafficking. Sterol transfer by lipid-binding proteins, such as OSBP (oxysterol-binding protein), coupled with phosphatidylinositol 4-phosphate exchange at membrane contact sites (MCSs) has emerged as a new theme of cholesterol transport between organellar membranes. Moreover, a previously unappreciated role of peroxisomes in cholesterol trafficking has been revealed recently. These discoveries highlight the crucial role of MCSs, or junctions, in facilitating lipid movement, and provide mechanistic insights into how cholesterol is sorted in cells.

摘要

胆固醇是一种必需的膜成分,在细胞信号转导中也起着关键作用。在细胞内,胆固醇如何运输以及其异质分布如何维持还知之甚少。最近的进展已经确定了胆固醇运输的新途径和调节因子。脂质结合蛋白(如 OSBP(氧化固醇结合蛋白))介导的固醇转移,与膜接触位点(MCS)处的磷酸肌醇 4-磷酸交换相结合,已成为细胞器膜之间胆固醇运输的新主题。此外,最近还揭示了过氧化物酶体在胆固醇运输中的以前未被认识到的作用。这些发现强调了 MCS 或连接在促进脂质运动中的关键作用,并为细胞中胆固醇如何分选提供了机制上的见解。

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