Department of Molecular Metabolism, Harvard T. H. Chan School of Public Health, Boston, Massachusetts 02115, USA
Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Cold Spring Harb Perspect Biol. 2023 May 2;15(5):a041246. doi: 10.1101/cshperspect.a041246.
More than 60 years ago, Eugene Kennedy and coworkers elucidated the endoplasmic reticulum (ER)-based pathways of glycerolipid synthesis, including the synthesis of phospholipids and triacylglycerols (TGs). The reactions of the Kennedy pathway were identified by studying the conversion of lipid intermediates and the isolation of biochemical enzymatic activities, but the molecular basis for most of these reactions was unknown. With recent progress in the cell biology, biochemistry, and structural biology in this area, we have a much more mechanistic understanding of this pathway and its reactions. In this review, we provide an overview of molecular aspects of glycerolipid synthesis, focusing on recent insights into the synthesis of TGs. Further, we go beyond the Kennedy pathway to describe the mechanisms for storage of TG in cytosolic lipid droplets and discuss how overwhelming these pathways leads to ER stress and cellular toxicity, as seen in diseases linked to lipid overload and obesity.
60 多年前,Eugene Kennedy 和他的同事阐明了甘油磷脂合成的内质网(ER)途径,包括磷脂和三酰基甘油(TGs)的合成。通过研究脂质中间体的转化和生化酶活性的分离,确定了 Kennedy 途径的反应,但这些反应的大多数分子基础尚不清楚。随着该领域在细胞生物学、生物化学和结构生物学方面的最新进展,我们对该途径及其反应有了更深入的机制理解。在这篇综述中,我们概述了甘油磷脂合成的分子方面,重点介绍了最近对 TG 合成的深入了解。此外,我们超越了 Kennedy 途径,描述了胞质脂滴中 TG 储存的机制,并讨论了这些途径如何导致内质网应激和细胞毒性,如与脂质过载和肥胖相关的疾病中所见。