Historical perspective: phosphatidylserine and phosphatidylethanolamine from the 1800s to the present

被引:75
作者
Vance, Jean E. [1 ,2 ]
机构
[1] Univ Alberta, Dept Med, Edmonton, AB T6G 2S2, Canada
[2] Univ Alberta, Grp Mol & Cell Biol Lipids, Edmonton, AB T6G 2S2, Canada
关键词
mitochondria; membranes; phosphoglycerolipids; phospholipid trafficking; ether lipids; MEMBRANE CONTACT SITES; MITOCHONDRIA-ASSOCIATED MEMBRANES; CTP-PHOSPHOETHANOLAMINE CYTIDYLYLTRANSFERASE; CDP-ETHANOLAMINE PATHWAY; ROUGH ENDOPLASMIC-RETICULUM; BASE-EXCHANGE ENZYME; ALKYL ETHER BONDS; RAT-LIVER; PHOSPHOLIPID-SYNTHESIS; SYNTHASE-I;
D O I
10.1194/jlr.R084004
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
This article provides a historical account of the discovery, chemistry, and biochemistry of two ubiquitous phosphoglycerolipids, phosphatidylserine (PS) and phosphatidylethanolamine (PE), including the ether lipids. In addition, the article describes the biosynthetic pathways for these phospholipids and how these pathways were elucidated. Several unique functions of PS and PE in mammalian cells in addition to their ability to define physical properties of membranes are discussed. For example, the translocation of PS from the inner to the outer leaflet of the plasma membrane of cells occurs during apoptosis and during some other specific physiological processes, and this translocation is responsible for profound life-or-death events. Moreover, mitochondrial function is severely impaired when the PE content of mitochondria is reduced below a threshold level. The discovery and implications of the existence of membrane contact sites between the endoplasmic reticulum and mitochondria and their relevance for PS and PE metabolism, as well as for mitochondrial function, are also discussed. Many of the recent advances in these fields are due to the use of isotope labeling for tracing biochemical pathways. In addition, techniques for disruption of specific genes in mice are now widely used and have provided major breakthroughs in understanding the roles and metabolism of PS and PE in vivo.
引用
收藏
页码:923 / 944
页数:22
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