南美超级胎牛血清999尝鲜特惠
转染试剂低至5折
基质胶阶梯特惠
积分商城,好礼送不停
南美超级胎牛血清999尝鲜特惠
转染试剂低至5折
基质胶阶梯特惠
积分商城,好礼送不停
分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

PFKL对脂质代谢的重新编程促进了胰腺导管腺癌对葡萄糖缺乏的适应性反应。

Reprogramming of lipid metabolism by PFKL promotes the adaptation of pancreatic ductal adenocarcinoma to glucose deprivation

Lu Chai, Zhaoyuan Meng, Zhimin Lu, Jing Fang

Journal:CELLULAR SIGNALLING

IF:4.7

DOI:10.1016/j.cellsig.2026.112839

PMID:42632532

Published:2026-08-22

research field:

Abstract

Background/Objective Lipid droplet (LD)–mitochondria tethering is essential for fatty acid oxidation (FAO), which sustains tumor cell survival under nutrient-deprivation conditions. However, how LD–mitochondria contact is regulated in pancreatic ductal adenocarcinoma (PDAC) is unclear. Methods This study investigated the signaling pathway that regulates lipid droplet-mitochondria interaction in PDAC under conditions of glucose deprivation, utilizing molecular interaction assays, cellular functional experiments, and clinical sample validation. Results Glucose deprivation activated p38, leading to phosphorylation of phosphofructokinase, liver type (PFKL) at T331, which in turn phosphorylated the LD protein perilipin 2 (PLIN2) at S159 in PDAC cells. This enhanced the binding of PLIN2 to mitochondrial protein carnitine palmitoyltransferase-1 A (CPT1A), thereby promoting LD–mitochondria tethering. Disruption of this axis impaired LD–mitochondria contact, reduced lipid consumption and ATP production, decreased cell viability, increased apoptosis, and suppressed tumor growth. In human PDAC samples, phosphorylation levels at both PFKL T331 and PLIN2 S159 were elevated and showed a positive correlation. Conclusion PFKL plays a key role in coordinating LD–mitochondria tethering under glucose deprivation in PDAC, and targeting the p38–PFKL–PLIN2–CPT1A axis may represent a promising therapeutic strategy.

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