磷脂酰乙醇胺
生物
自噬
磷脂酰丝氨酸
细胞生物学
生物发生
粒体自噬
线粒体
氧化磷酸化
细胞器
生物化学
磷脂
磷脂酰胆碱
细胞凋亡
膜
基因
作者
Elizabeth Calzada,Ouma Onguka,Steven M. Claypool
标识
DOI:10.1016/bs.ircmb.2015.10.001
摘要
Phosphatidylethanolamine (PE) is the second most abundant glycerophospholipid in eukaryotic cells. The existence of four only partially redundant biochemical pathways that produce PE, highlights the importance of this essential phospholipid. The CDP-ethanolamine and phosphatidylserine decarboxylase pathways occur in different subcellular compartments and are the main sources of PE in cells. Mammalian development fails upon ablation of either pathway. Once made, PE has diverse cellular functions that include serving as a precursor for phosphatidylcholine and a substrate for important posttranslational modifications, influencing membrane topology, and promoting cell and organelle membrane fusion, oxidative phosphorylation, mitochondrial biogenesis, and autophagy. The importance of PE metabolism in mammalian health has recently emerged following its association with Alzheimer's disease, Parkinson's disease, nonalcoholic liver disease, and the virulence of certain pathogenic organisms.
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