Kitasato University School of Medicine, Sagamihara 252-0374, Kanagawa, Japan.
Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai 980-8578, Miyagi, Japan.
Nat Commun. 2024 Apr 2;15(1):2843. doi: 10.1038/s41467-024-46971-9.
Glycolysis is a fundamental cellular process, yet its regulatory mechanisms remain incompletely understood. Here, we show that a subset of glucose transporter 1 (GLUT1/SLC2A1) co-endocytoses with platelet-derived growth factor (PDGF) receptor (PDGFR) upon PDGF-stimulation. Furthermore, multiple glycolytic enzymes localize to these endocytosed PDGFR/GLUT1-containing vesicles adjacent to mitochondria. Contrary to current models, which emphasize the importance of glucose transporters on the cell surface, we find that PDGF-stimulated glucose uptake depends on receptor/transporter endocytosis. Our results suggest that growth factors generate glucose-loaded endocytic vesicles that deliver glucose to the glycolytic machinery in proximity to mitochondria, and argue for a new layer of regulation for glycolytic control governed by cellular membrane dynamics.
糖酵解是一种基本的细胞过程,但它的调节机制仍不完全清楚。在这里,我们表明,血小板衍生生长因子(PDGF)受体(PDGFR)在 PDGF 刺激时,一部分葡萄糖转运蛋白 1(GLUT1/SLC2A1)与 PDGFR 共内吞。此外,多种糖酵解酶定位于这些靠近线粒体的内吞 PDGFR/GLUT1 含囊泡中。与目前强调细胞表面葡萄糖转运体重要性的模型相反,我们发现 PDGF 刺激的葡萄糖摄取依赖于受体/转运体的内吞作用。我们的结果表明,生长因子产生富含葡萄糖的内吞囊泡,将葡萄糖递送至靠近线粒体的糖酵解机器,这为受细胞膜动力学调控的糖酵解控制提供了一个新的调控层。