Wei Fujing, Duan Yixiang
Research Center of Analytical Instrumentation, Key Laboratory of Bio-resource and Eco-enviroment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, 610065, Sichuan, P. R. China.
Adv Biosyst. 2019 Jan;3(1):e1800259. doi: 10.1002/adbi.201800259. Epub 2018 Nov 4.
Nanomaterials (NMs) are comprehensively applied in biomedicine due to their unique physical and chemical properties. Autophagy, as an evolutionarily conserved cellular quality control process, is closely associated with the effect of NMs on cells. In this review, the recent advances in NM-induced/inhibited autophagy (NM-phagy) are summarized, with an aim to present a comprehensive description of the mechanisms of NM-phagy from the perspective of internalization, activation, and termination, thereby bridging autophagy and nanomaterials. Several possible mechanisms are extensively reviewed including the endocytosis pathway of NMs and the related cross components (clathrin and adaptor protein 2 (AP-2), adenosine diphosphate (ADP)-ribosylation factor 6 (Arf6), Rab, UV radiation resistance associated gene (UVRAG)), three main stress mechanisms (oxidative stress, damaged organelles stress, and toxicity stress), and several signal pathway-related molecules. The mechanistic insight is beneficial to understand the autophagic response to NMs or NMs' regulation of autophagy. The challenges currently encountered and research trend in the field of NM-phagy are also highlighted. It is hoped that the NM-phagy discussion in this review with the focus on the mechanistic aspects may serve as a guideline for future research in this field.
由于其独特的物理和化学性质,纳米材料(NMs)在生物医学中得到了广泛应用。自噬作为一种进化上保守的细胞质量控制过程,与纳米材料对细胞的影响密切相关。在本综述中,总结了纳米材料诱导/抑制自噬(纳米材料自噬)的最新进展,旨在从内化、激活和终止的角度全面描述纳米材料自噬的机制,从而在自噬和纳米材料之间架起桥梁。广泛综述了几种可能的机制,包括纳米材料的内吞途径及相关交叉成分(网格蛋白和衔接蛋白2(AP-2)、二磷酸腺苷(ADP)-核糖基化因子6(Arf6)、Rab、紫外线抗性相关基因(UVRAG))、三种主要应激机制(氧化应激、受损细胞器应激和毒性应激)以及几种信号通路相关分子。对机制的深入了解有助于理解对纳米材料的自噬反应或纳米材料对自噬的调节。还强调了纳米材料自噬领域目前遇到的挑战和研究趋势。希望本综述中围绕机制方面展开的纳米材料自噬讨论能够为该领域未来的研究提供指导。