Kessel David
Wayne State University School of Medicine, Detroit, MI, USA.
Photochem Photobiol. 2021 Sep;97(5):1097-1100. doi: 10.1111/php.13438. Epub 2021 May 18.
Two cell lines, A549 (human-derived nonsmall-cell lung cancer) and 1c1c7 (mouse hepatoma), were photosensitized with m-THPC and irradiated under LD conditions. After 4 h, a pattern of cytoplasmic vacuoles had formed consistent with the initiation of paraptosis. After irradiation, there was no detectable loss of the mitochondrial membrane potential indicating no significant photodamage to mitochondria. We did, however, observe localization of m-THPC in the endoplasmic reticulum (ER), as indicated by fluorescence microscopy. Subsequent ER perturbation is known to result in initiation of paraptosis, another pathway to cell death. While an apoptotic response to m-THPC has been reported, the ability to target ER and induce paraptosis could explain the efficacy of this agent which could therefore eradicate cell types with an impaired apoptotic response.
两种细胞系,A549(人源非小细胞肺癌)和1c1c7(小鼠肝癌),用间四羟基苯基氯卟啉(m-THPC)进行光敏化处理,并在低剂量(LD)条件下进行照射。4小时后,形成了与副凋亡起始一致的细胞质空泡模式。照射后,未检测到线粒体膜电位的损失,表明线粒体没有明显的光损伤。然而,通过荧光显微镜观察,我们确实观察到m-THPC定位于内质网(ER)。已知随后的内质网扰动会导致副凋亡的起始,这是另一条细胞死亡途径。虽然已经报道了对m-THPC的凋亡反应,但靶向内质网并诱导副凋亡的能力可以解释这种药物的疗效,因此它可以根除凋亡反应受损的细胞类型。