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三者成派对:溶酶体、脂滴和内质网在脂质运输和细胞动态平衡中的作用。

And three's a party: lysosomes, lipid droplets, and the ER in lipid trafficking and cell homeostasis.

机构信息

University of Texas Southwestern Medical Center, Department of Cell Biology, Dallas, TX, 75390, USA.

出版信息

Curr Opin Cell Biol. 2019 Aug;59:40-49. doi: 10.1016/j.ceb.2019.02.011. Epub 2019 Apr 16.

Abstract

Sterols and fatty acids (FAs) are essential lipids that play fundamental roles in membrane dynamics and cellular homeostasis. Synthesized at the endoplasmic reticulum (ER) and cytoplasm, trafficked by proteins, and stored in lipid droplets (LDs), much work has been conducted examining how these lipids are shuttled from one location to another. Recent work has highlighted the importance of inter-organelle crosstalk in the regulation of sterol and FA homeostasis. In particular, three organelles-lysosomes, LDs, and the ER network-function together to regulate sterol subcellular distribution and utilization. This tri-organelle crosstalk also drives adaptions to stress and protects against FA-induced lipotoxicity. Here, we highlight recent work revealing how this unique organelle trio function together. We also discuss how LDs can modulate lysosome signaling to control growth, autophagy, and ER homeostasis.

摘要

甾醇和脂肪酸(FAs)是必不可少的脂质,在膜动力学和细胞内稳态中发挥着基本作用。它们在内质网(ER)和细胞质中合成,通过蛋白质运输,并储存在脂滴(LDs)中。许多研究都在研究这些脂质如何从一个位置转移到另一个位置。最近的工作强调了细胞器间通讯在固醇和 FA 内稳态调节中的重要性。特别是,三个细胞器——溶酶体、LDs 和 ER 网络——共同调节固醇的亚细胞分布和利用。这种三细胞器通讯还驱动了对压力的适应,并防止 FA 诱导的脂毒性。在这里,我们强调了最近的工作,揭示了这种独特的细胞器三重奏是如何协同工作的。我们还讨论了 LDs 如何调节溶酶体信号来控制生长、自噬和 ER 内稳态。

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