Lee Heejeong, Woo Eun-Rhan, Lee Dong Gun
School of Life Sciences, BK 21 Plus KNU Creative BioResearch Group, College of Natural Sciences, Kyungpook National University, Daehak-ro 80, Buk-gu, Daegu 702-701, Republic of Korea.
College of Pharmacy, Chosun University, 375 Seosuk-dong, Dong-gu, Gwangju 501-759, Republic of Korea.
FEMS Yeast Res. 2016 May;16(3). doi: 10.1093/femsyr/fow013. Epub 2016 Feb 15.
This study analyzes the antifungal properties of (-)-nortrachelogenin and elucidates its mode of action against pathogenic fungi. We performed susceptibility tests against several pathogenic fungi and verified the absence of hemolysis against human erythrocytes. Its antifungal activity increased reactive oxygen species (ROS) in response to intracellular stress and increased concentrations of both intracellular and extracellular trehalose without causing hemolysis. In addition, a cell wall regeneration study indicated its action on the cytoplasmic membrane. A cell surface study using 3,3(')-dipropylthiacarbocyanine iodide [DiSC3(5)] and 1,6-diphenyl-1,3,5-hexatriene (DPH) demonstrated dissipation of the cytoplasmic membrane at high concentrations. Our study revealed a disturbance in the membrane at higher concentrations and externalization of phosphatidylserine in a dose-dependent manner, affecting other intracellular responses. Furthermore, we investigated the late stage of apoptosis using TUNEL and 4('),6-diamidino-2-phenylindole (DAPI) assays. (-)-Nortrachelogenin-treated cells underwent apoptosis which was triggered by mitochondrial dysfunction via depolarization of the mitochondrial membrane, release of cytochrome c and calcium ion signaling, resulting in the activation of metacaspases. Different concentrations of (-)-nortrachelogenin induced membrane disruption and caspase-dependent apoptosis.
本研究分析了(-)-去甲rachelogenin的抗真菌特性,并阐明了其对致病真菌的作用模式。我们对几种致病真菌进行了药敏试验,并验证了其对人红细胞无溶血作用。其抗真菌活性在细胞内应激时增加活性氧(ROS),并增加细胞内和细胞外海藻糖的浓度,且不引起溶血。此外,细胞壁再生研究表明其作用于细胞质膜。使用3,3'-二丙基硫代碳菁碘化物[DiSC3(5)]和1,6-二苯基-1,3,5-己三烯(DPH)进行的细胞表面研究表明,高浓度时细胞质膜会发生耗散。我们的研究揭示了高浓度时膜的紊乱以及磷脂酰丝氨酸以剂量依赖方式外化,影响其他细胞内反应。此外,我们使用TUNEL和4',6-二脒基-2-苯基吲哚(DAPI)检测法研究了凋亡后期。(-)-去甲rachelogenin处理的细胞发生凋亡,这是由线粒体功能障碍引发的,通过线粒体膜去极化、细胞色素c释放和钙离子信号传导,导致metacaspases激活。不同浓度的(-)-去甲rachelogenin诱导膜破坏和caspase依赖性凋亡。