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基于 Au@Pt 纳米管网络的可拉伸电极用于实时监测内皮细胞机械转导中的 ROS 信号。

Stretchable Electrode Based on Au@Pt Nanotube Networks for Real-Time Monitoring of ROS Signaling in Endothelial Mechanotransduction.

机构信息

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.

College of Chemistry and Chemical Engineering, Xinyang Normal University, Xinyang 464000, China.

出版信息

Anal Chem. 2020 Dec 1;92(23):15639-15646. doi: 10.1021/acs.analchem.0c04015. Epub 2020 Nov 12.

DOI:10.1021/acs.analchem.0c04015
PMID:33179904
Abstract

Vascular endothelial cells (ECs) are natively exposed to dynamic cyclic stretch and respond to it by the production of vasoactive molecules. Among them, reactive oxygen species (ROS) are closely implicated to the endothelial function and vascular homeostasis. However, the dynamic monitoring of ROS release during endothelial mechanotransduction remains a steep challenge. Herein, we developed a stretchable electrochemical sensor by decoration of uniform and ultrasmall platinum nanoparticles (Pt NPs) on gold nanotube (Au NT) networks (denoted as Au@Pt NTs). The orchestrated structure exhibited prominent electrocatalytic property toward the oxidation of hydrogen peroxide (HO) (as the most stable ROS) while maintaining excellent mechanical compliance of Au NT networks. Moreover, the favorable biocompatibility of Au NTs and Pt NPs promoted the adhesion and proliferation of ECs cultured thereon. These allowed in situ inducing ECs mechanotransduction and synchronously real-time monitoring of HO release. Further investigation revealed that the production of HO was positively correlated with the applied mechanical strains and could be boosted by other coexisting pathogenic factors. This indicates the great prospect of our proposed sensor in exploring ROS-related signaling for the deep understanding of cell mechanotransduction and vascular disorder.

摘要

血管内皮细胞(ECs)天然地暴露于动态循环拉伸下,并通过产生血管活性分子来对此做出反应。其中,活性氧(ROS)与内皮功能和血管稳态密切相关。然而,在细胞力学转导过程中对 ROS 释放的动态监测仍然是一个巨大的挑战。在此,我们通过在金纳米管(Au NT)网络上修饰均匀且超小的铂纳米颗粒(Pt NPs),开发了一种可拉伸的电化学传感器(表示为 Au@Pt NTs)。协调的结构对过氧化氢(HO)(作为最稳定的 ROS)的氧化表现出突出的电催化性能,同时保持 Au NT 网络的优异机械顺应性。此外,Au NTs 和 Pt NPs 的良好生物相容性促进了其上培养的 ECs 的黏附和增殖。这使得能够原位诱导 EC 力学转导并同步实时监测 HO 的释放。进一步的研究表明,HO 的产生与施加的机械应变呈正相关,并且可以被其他共存的致病因素所促进。这表明我们提出的传感器在探索与 ROS 相关的信号方面具有广阔的前景,有助于深入了解细胞力学转导和血管紊乱。

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