Specialized ER membrane domains for lipid metabolism and transport

被引:18
|
作者
Nishimura, Taki [1 ,2 ]
Stefan, Christopher J. [1 ]
机构
[1] UCL, MRC, Lab Mol Cell Biol, Gower St, London WC1E 6BT, England
[2] Francis Crick Inst, Mol Cell Biol Autophagy, London NW1 1AT, England
关键词
Endoplasmic reticulum; Phospholipid biosynthesizing enzyme; Lipid transfer protein; Membrane contact sites; Plasma membrane; OXYSTEROL-BINDING-PROTEIN; PHOSPHATIDYLINOSITOL-TRANSFER PROTEIN; PLASMA-MEMBRANE; CONTACT SITES; SACCHAROMYCES-CEREVISIAE; PHOSPHOLIPID-SYNTHESIS; CRYSTAL-STRUCTURE; PHOSPHATIDYLSERINE TRANSPORT; NONVESICULAR TRAFFICKING; AUTOPHAGOSOME FORMATION;
D O I
10.1016/j.bbalip.2019.07.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The endoplasmic reticulum (ER) is a highly organized organelle that performs vital functions including de novo membrane lipid synthesis and transport. Accordingly, numerous lipid biosynthesis enzymes are localized in the ER membrane. However, it is now evident that lipid metabolism is sub-compartmentalized within the ER and that lipid biosynthetic enzymes engage with lipid transfer proteins (LTPs) to rapidly shuttle newly synthesized lipids from the ER to other organelles. As such, intimate relationships between lipid metabolism and lipid transfer pathways exist within the ER network. Notably, certain LTPs enhance the activities of lipid metabolizing enzymes; likewise, lipid metabolism can ensure the specificity of LTP transfer/exchange reactions. Yet, our understanding of these mutual relationships is still emerging. Here, we highlight past and recent key findings on specialized ER membrane domains involved in efficient lipid metabolism and transport and consider unresolved issues in the field.
引用
收藏
页数:12
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