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引用次数: 0
摘要
由于细胞死亡是一种不可避免的现象,因此探索细胞死亡具有重要意义。在这一过程中,细胞内的微环境(如 pH 值、极性、粘度等)会发生变化。在不同的细胞死亡过程中,粘度会升高,这就是微环境之一。然而,仅根据粘度感应来划分细胞死亡过程具有挑战性。在此,我们对三种类似物进行了仔细研究,开发出一种独特的荧光探针 PS-NAP,用于对 HeLa 细胞进行有效的粘度成像。阳离子 PS-NAP 是一种不依赖于 MMP 的分子探针,可在细胞凋亡、饥饿和药物诱导的铁突变过程中靶向线粒体并绘制线粒体粘度升高图。值得注意的是,在半胱氨酸匮乏诱导的铁凋亡过程中,PS-NAP只聚集在新生成的脂滴(LD)中,而不是线粒体中。因此,该探针有望将半胱氨酸匮乏诱导的铁凋亡与细胞凋亡等其他细胞压力区分开来。
A Fluorescent Probe Differentiates Apoptosis from Cysteine-Deprivation Ferroptosis through Imaging of Viscosity and Lipid Droplets.
Since death is an inevitable phenomenon, exploring cell deaths holds importance. During this process, the cellular microenvironment within cells such as pH, polarity, viscosity etc alter. One such microenvironment, viscosity elevates during different cell deaths. However, demarcating cell death processes solely based on viscosity sensing is challenging. Herein, we develop a unique fluorescent probe PS-NAP after careful investigation among three analogues for efficient viscosity imaging in HeLa cells. Cationic PS-NAP, a MMP independent molecular probe, can potentially target mitochondria and map elevated mitochondrial viscosity during apoptosis, starvation and drug induced ferroptosis processes. Notably, during ferroptosis induced by cysteine deprivation, PS-NAP exclusively colocalizes in newly generated lipid droplets (LDs) instead of mitochondria. Thus, the probe has a potential for demarcating cysteine deprivation-induced ferroptosis from other cellular stresses such as apoptosis.
期刊介绍:
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