化学
脂滴
二酰甘油激酶
分解代谢
细胞器
脂解
荧光
荧光显微镜
脂肪甘油三酯脂肪酶
生物物理学
脂质代谢
甘油二酯
生物化学
水解
光漂白后的荧光恢复
脂肪酶
甘油三酯
自噬
费斯特共振能量转移
微粘度
活体细胞成像
荧光寿命成像显微镜
动力学
脂毒性
分区(防火)
溶酶体
磷脂酰乙醇胺
新陈代谢
色谱法
油滴
溶血磷脂酰乙醇胺
酶
脂质微区
磷脂
细胞生物学
作者
Junwei Wang,Keiji Kajiwara,Manish Kesherwani,Florence Tama,Yuki Ohsaki,Shigehiro Yamaguchi,Masayasu Taki
摘要
Lipid droplets (LDs) are dynamic organelles essential to lipid metabolism and energy homeostasis, yet their compositional heterogeneity in living cells remains poorly understood. Here, we present LipiPB Red, a red-emissive fluorescent probe with exceptional photostability, high polarity sensitivity, and long-term retention within LDs, even under serum-containing conditions. When applied to fluorescence lifetime imaging microscopy (FLIM), LipiPB Red enables discrimination between triacylglycerol (TAG) and diacylglycerol (DAG) content within individual LDs. FLIM analysis revealed pronounced compositional heterogeneity among LDs in hepatoma cells. This heterogeneity was abolished, with a concomitant increase in average fluorescence lifetimes, upon genetic knockdown or pharmacological inhibition of adipose triglyceride lipase (ATGL), implicating ATGL-mediated lipolysis as a key regulator of LD diversity. Moreover, coimaging with autophagy markers revealed reduced fluorescence lifetimes in LDs localized within both autophagosomes and autolysosomes. These findings indicate a sequential lipid degradation cascade during lipophagy, where lipid hydrolysis is initiated prior to lysosomal fusion.
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