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不可生物降解纳米颗粒、活性氧物种和自噬之间的分子联系。

Molecular links among non-biodegradable nanoparticles, reactive oxygen species, and autophagy.

机构信息

Department of Chemical and Biomolecular Engineering, University of Tennessee, 1512 Middle Drive, Knoxville, TN 37996-2200, USA.

Department of Chemical and Biomolecular Engineering, University of Tennessee, 1512 Middle Drive, Knoxville, TN 37996-2200, USA; Department of Biochemistry, Cellular and Molecular Biology, University of Tennessee, 1414 Cumberland Avenue, Knoxville, TN 37996, USA.

出版信息

Adv Drug Deliv Rev. 2017 Dec 1;122:65-73. doi: 10.1016/j.addr.2017.01.001. Epub 2017 Jan 6.

Abstract

For nanoparticles to be successful in combating diseases in the clinic in the 21st century and beyond, they must localize to target areas of the body and avoid damaging non-target, healthy tissues. Both soft and stiff, bio-degradable and non-biodegradable nanoparticles are anticipated to be used to this end. It has been shown that stiff, non-biodegradable nanoparticles cause reactive oxygen species (ROS) generation and autophagy in a variety of cell lines in vitro. Both responses can lead to significant remodeling of the cytosol and even apoptosis. Thus these are crucial cellular functions to understand. Improved assays have uncovered crucial roles of the Akt/mTOR signaling pathway in both ROS generation and autophagy initiation after cells have internalized stiff, non-biodegradable nanoparticles over varying geometries in culture. Of particular - yet unresolved - interest is how these nanoparticles cause the activation of these pathways. This article reviews the most recent advances in nanoparticle generation of ROS and autophagy initiation with a focus on stiff, non-biodegradable technologies. We provide experimental guidelines to the reader for fleshing out the effects of their nanoparticles on the above pathways with the goal of tuning nanoparticle design.

摘要

为了使纳米粒子在 21 世纪及以后能够成功地用于临床治疗疾病,它们必须定位于身体的靶区,并避免损害非靶标、健康的组织。预计将使用软的和硬的、可生物降解的和不可生物降解的纳米粒子来实现这一目标。已经表明,硬的、不可生物降解的纳米粒子在体外的各种细胞系中引起活性氧(ROS)的产生和自噬。这两种反应都可能导致细胞质的显著重塑,甚至凋亡。因此,这些是理解的关键细胞功能。改进的测定方法揭示了 Akt/mTOR 信号通路在细胞内化不同形状的硬的、不可生物降解的纳米粒子后,ROS 的产生和自噬起始中的关键作用。特别但尚未解决的问题是这些纳米粒子如何导致这些途径的激活。本文综述了硬的、不可生物降解的纳米技术在 ROS 生成和自噬起始方面的最新进展。我们为读者提供了实验指南,以阐述他们的纳米粒子对上述途径的影响,目的是调整纳米粒子的设计。

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