Nanoparticles modulate autophagic effect in a dispersity-dependent manner

作者：Huang, Dengtong; Zhou, Hualu; Gao, Jinhao^*

来源：Scientific Reports, 2015, 5(1): 14361.

DOI：10.1038/srep14361

• SILICA NANOPARTICLES
• GOLD NANOPARTICLES
• THERAPEUTIC TARGET
• CELLS
• NANOCRYSTALS
• SIZE
• AGGREGATION
• INHIBITOR
• TOXICITY
• TURNOVER

Autophagy plays a key role in human health and disease, especially in cancer and neurodegeneration. Many autophagy regulators are developed for therapy. Diverse nanomaterials have been reported to induce autophagy. However, the underlying mechanisms and universal rules remain unclear. Here, for the first time, we show a reliable and general mechanism by which nanoparticles induce autophagy and then successfully modulate autophagy via tuning their dispersity. Various well-designed univariate experiments demonstrate that nanomaterials induce autophagy in a dispersity-dependent manner. Aggregated nanoparticles induce significant autophagic effect in comparison with well-dispersed nanoparticles. As the highly stable nanoparticles may block autophagic degradation in autolysosomes, endocytosis and intracellular accumulation of nanoparticles can be responsible for this interesting phenomenon. Our results suggest dispersity-dependent autophagic effect as a common cellular response to nanoparticles, reveal the relationship between properties of nanoparticles and autophagy, and offer a new alternative way to modulate autophagy.

• 出版日期2015-9-23
• 单位厦门大学