石墨烯量子点作为自噬诱导的光动力剂。
Graphene quantum dots as autophagy-inducing photodynamic agents.
机构信息
Vinca Institute of Nuclear Sciences, University of Belgrade, 11000 Belgrade, Serbia.
出版信息
Biomaterials. 2012 Oct;33(29):7084-92. doi: 10.1016/j.biomaterials.2012.06.060. Epub 2012 Jul 15.
The excellent photoluminescent properties of graphene quantum dots (GQD) makes them suitable candidates for biomedical applications, but their cytotoxicity has not been extensively studied. Here we show that electrochemically produced GQD irradiated with blue light (470 nm, 1W) generate reactive oxygen species, including singlet oxygen, and kill U251 human glioma cells by causing oxidative stress. The cell death induced by photoexcited GQD displayed morphological and/or biochemical characteristics of both apoptosis (phosphatidylserine externalization, caspase activation, DNA fragmentation) and autophagy (formation of autophagic vesicles, LC3-I/LC3-II conversion, degradation of autophagic target p62). Moreover, a genetic inactivation of autophagy-essential LC3B protein partly abrogated the photodynamic cytotoxicity of GQD. These data indicate potential usefulness of GQD in photodynamic therapy, but also raise concerns about their possible toxicity.
石墨烯量子点(GQD)具有优异的光致发光性能,使其成为生物医学应用的候选者,但它们的细胞毒性尚未得到广泛研究。在这里,我们表明,用蓝光(470nm,1W)照射电化学产生的 GQD 会产生活性氧,包括单线态氧,并通过氧化应激杀死 U251 人神经胶质瘤细胞。由光激发的 GQD 诱导的细胞死亡表现出凋亡(磷脂酰丝氨酸外翻、半胱天冬酶激活、DNA 片段化)和自噬(自噬小体形成、LC3-I/LC3-II 转化、自噬靶标 p62 降解)的形态学和/或生化特征。此外,自噬必需的 LC3B 蛋白的遗传失活部分消除了 GQD 的光动力细胞毒性。这些数据表明 GQD 在光动力疗法中有潜在的用途,但也引起了对其可能毒性的关注。