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自噬受内质网钙离子稳态和鞘脂代谢调节。

Autophagy is regulated by endoplasmic reticulum calcium homeostasis and sphingolipid metabolism.

机构信息

Department of Neurosurgery, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

Department of Laboratory Medicine, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

出版信息

Autophagy. 2023 Dec;19(12):3256-3257. doi: 10.1080/15548627.2023.2249761. Epub 2023 Aug 23.

Abstract

Calcium is involved in a variety of cellular processes. As the crucial components of cell membranes, sphingolipids also play important roles as signaling molecules. Intracellular calcium homeostasis, autophagy initiation and sphingolipid synthesis are associated with the endoplasmic reticulum (ER). Recently, through genetic screening and lipidomics analysis in , we found that the ER calcium channel Csg2 converts sphingolipid metabolism into macroautophagy/autophagy regulation by controlling ER calcium homeostasis. The results showed that Csg2 acts as a calcium channel to mediate ER calcium efflux into the cytoplasm, and deletion of causes a distinct increase of ER calcium concentration, thereby disrupting the stability of the sphingolipid synthase Aur1, leading to the accumulation of the bioactive sphingolipid phytosphingosine (PHS), which specifically and completely blocks autophagy. In summary, our work links calcium homeostasis, sphingolipid metabolism, and autophagy initiation via the ER calcium channel Csg2.

摘要

钙参与多种细胞过程。鞘脂类作为细胞膜的重要组成部分,也作为信号分子发挥重要作用。细胞内钙稳态、自噬起始和鞘脂合成与内质网(ER)有关。最近,通过在 中的遗传筛选和脂质组学分析,我们发现 ER 钙通道 Csg2 通过控制 ER 钙稳态将鞘脂代谢转化为巨自噬/自噬调节。结果表明,Csg2 作为钙通道介导 ER 钙向细胞质流出,而 的缺失导致 ER 钙浓度明显增加,从而破坏了鞘脂合酶 Aur1 的稳定性,导致生物活性鞘脂植物鞘氨醇(PHS)的积累,特异性和完全阻断自噬。总之,我们的工作通过 ER 钙通道 Csg2 将钙稳态、鞘脂代谢和自噬起始联系起来。

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