Abstract
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.
Highlights
TO PHOSPHOLIPID BIOSYNTHESISBiological membranes contain a vast array of different lipids: for example, membranes of mammalian cells contain more than a thousand different phosphoglycerolipids
Because Pisd+/ heterozygous mice appeared to be normal in all respects, whereas complete elimination of PS decarboxylase (PSD) was 100% embryonically lethal, we reduced PSD activity in Chinese hamster ovary (CHO) cells by 85% using siRNA silencing so that we could determine the impact of reducing mitochondrial PE content
I have focused on the remarkable historical background on the discovery and chemistry of two phosphoglycerolipids, PS and PE, and have provided an account of the step-wise elucidation of the biosynthetic pathways for PS and PE in mammalian cells
Summary
Biological membranes contain a vast array of different lipids: for example, membranes of mammalian cells contain more than a thousand different phosphoglycerolipids. It is known that approximately 20% of mitochondria in HeLa cells are normally in close juxtaposition with the ER, at a separation of 20–30 nm [99] In these subcellular fractionation experiments, we were investigating the subcellular location of enzymes involved in phospholipid synthesis in rat liver, and were aware that PS synthase activity had previously been localized to microsomal membranes [100, 101]. PE is a precursor of anandamide (N-arachidonoylethanolamine) [294], a ligand for cannabinoid receptors in the brain
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