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随心所欲:按需合成磷脂驱动自噬体的扩张。

As (and when) you like it: on-demand phospholipid synthesis drives phagophore expansion during autophagy.

机构信息

Life Sciences Institute and Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.

出版信息

Autophagy. 2020 May;16(5):779-781. doi: 10.1080/15548627.2020.1732713. Epub 2020 Feb 25.

Abstract

A key feature of macroautophagy/autophagy is the formation of a transient compartment called the phagophore, which envelops cytoplasmic material, ultimately enclosing it within an autophagosome, allowing it to be targeted for degradation. Schütter describe a novel mechanism that spatiotemporally coordinates phospholipid synthesis to drive phagophore expansion and autophagosome formation. These authors show that during starvation, fatty acids (FAs) are channeled into phospholipid synthesis, and the newly synthesized lipids are directed toward autophagosome biogenesis.: ACS: acyl-CoA synthetase; ER: endoplasmic reticulum; FA: fatty acid; FAS: fatty acid synthetase; MCS: membrane contact sites; PAS: phagophore assembly site.

摘要

自噬的一个关键特征是形成一个短暂的隔室,称为吞噬体,它包裹细胞质物质,最终将其封闭在自噬体中,使其能够被降解。Schütter 描述了一种新的机制,该机制在时空上协调磷脂合成以驱动吞噬体扩张和自噬体形成。这些作者表明,在饥饿期间,脂肪酸(FA)被引导进入磷脂合成,新合成的脂质被定向用于自噬体发生。:ACS:酰基辅酶 A 合成酶;ER:内质网;FA:脂肪酸;FAS:脂肪酸合成酶;MCS:膜接触位点;PAS:吞噬体组装位点。

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本文引用的文献

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