Zeineh Nidal, Nagler Rafael M, Gabay Martin, Obeid Fadi, Kahana Meygal, Weizman Abraham, Gavish Moshe
Department of Neuroscience, The Ruth and Bruce Rappaport Faculty of Medicine, Technion Institute of Technology, Haifa 31096, Israel.
Research Unit, Geha Mental Health Center and Laboratory of Biological Psychiatry, Felsenstein Medical Research Center, Petah Tikva 4910002, Israel.
Biology (Basel). 2021 May 2;10(5):395. doi: 10.3390/biology10050395.
TSPO is involved in cigarette smoke (CS)-induced cellular toxicity, which may result in oral and pulmonary diseases and lung cancer. H1299 lung cancer cells were exposed directly to CS. The H1299 cells were pretreated with our TSPO ligands MGV-1 and 2-Cl-MGV-1 (Ki = 825 nM for both) at a concentration of 25 µM 24 h prior to CS exposure. Cell death and apoptotic markers were measured, in addition to TSPO expression levels, ATP synthase activity, generation of reactive oxygen species (ROS), depolarization of mitochondrial membrane potential (ΔΨm), cAMP and LDH levels. Pretreatment with MGV-1 and 2-Cl-MGV-1 (25 µM), 24 h prior to CS exposure, differentially attenuated the CS-induced cellular insult as well as cell death in H1299 lung cancer cells. These protective effects included prevention of ATP synthase reversal, ROS generation, depolarization of the mitochondrial membrane and elevation in LDH. The preventive efficacy of 2-Cl-MGV-1 was superior to that achieved by MGV-1. Both ligands did not prevent the elevation in cAMP. These findings may indicate a mild protective effect of these TSPO ligands in CS-related pulmonary and keratinocyte cellular pathology.
转运蛋白18 kDa(TSPO)参与香烟烟雾(CS)诱导的细胞毒性,这可能导致口腔和肺部疾病以及肺癌。将H1299肺癌细胞直接暴露于CS中。在暴露于CS前24小时,用我们的TSPO配体MGV-1和2-氯-MGV-1(两者的Ki均为825 nM)以25μM的浓度对H1299细胞进行预处理。除了测量TSPO表达水平、ATP合酶活性、活性氧(ROS)生成、线粒体膜电位(ΔΨm)去极化、cAMP和乳酸脱氢酶(LDH)水平外,还检测了细胞死亡和凋亡标志物。在暴露于CS前24小时用MGV-1和2-氯-MGV-1(25μM)进行预处理,可不同程度地减轻CS诱导的H1299肺癌细胞的细胞损伤以及细胞死亡。这些保护作用包括防止ATP合酶逆转、ROS生成、线粒体膜去极化以及LDH升高。2-氯-MGV-1的预防效果优于MGV-1。两种配体均不能阻止cAMP升高。这些发现可能表明这些TSPO配体在CS相关的肺部和角质形成细胞病理学中具有轻度保护作用。