School of Medicine and Public Health, University of Wisconsin-Madison, 1111 Highland Avenue, Madison, WI 53705, USA.
Department of Medicine, University of Wisconsin Carbone Cancer Center, School of Medicine and Public Health, University of Wisconsin-Madison, 1111 Highland Avenue, Madison, WI 53705, USA.
Biomolecules. 2023 Aug 24;13(9):1297. doi: 10.3390/biom13091297.
Cytoplasmic phosphoinositides () are critical regulators of the membrane-cytosol interface that control a myriad of cellular functions despite their low abundance among phospholipids. The metabolic cycle that generates different PI species is crucial to their regulatory role, controlling membrane dynamics, vesicular trafficking, signal transduction, and other key cellular events. The synthesis of phosphatidylinositol (3,4,5)-triphosphate (PI3,4,5P) in the cytoplamic PI3K/Akt pathway is central to the life and death of a cell. This review will focus on the emerging evidence that scaffold proteins regulate the PI3K/Akt pathway in distinct membrane structures in response to diverse stimuli, challenging the belief that the plasma membrane is the predominant site for PI3k/Akt signaling. In addition, we will discuss how PIs regulate the recruitment of specific scaffolding complexes to membrane structures to coordinate vesicle formation, fusion, and reformation during autophagy as well as a novel lysosome repair pathway.
细胞质磷酸肌醇()是控制膜细胞质界面的关键调节剂,尽管它们在磷脂中的含量较低,但它们控制着众多的细胞功能。生成不同 PI 物种的代谢循环对其调节作用至关重要,控制膜动力学、囊泡运输、信号转导和其他关键细胞事件。细胞质中 PI3K/Akt 途径中磷脂酰肌醇(3,4,5)-三磷酸(PI3,4,5P)的合成对细胞的生死存亡至关重要。本综述将重点介绍新出现的证据,即支架蛋白在响应不同刺激时在不同的膜结构中调节 PI3K/Akt 途径,这挑战了质膜是 PI3k/Akt 信号传导的主要场所的观点。此外,我们还将讨论 PI 如何调节特定支架复合物募集到膜结构,以协调自噬过程中囊泡的形成、融合和再形成,以及新的溶酶体修复途径。