Analysis of vibrational dynamics in cell-substrate interactions using nanopipette electrochemical sensors

被引:1
|
作者
Gong, Li -Juan [1 ]
Lv, Jian [1 ]
Wang, Xiao-Yuan [1 ]
Wu, Xue [1 ]
Li, Da -Wei [1 ]
Qian, Ruo-Can [1 ]
机构
[1] East China Univ Sci & Technol, Frontiers Sci Ctr Materiobiol & Dynam Chem, Sch Chem & Mol Engn, Joint Res Ctr,Key Lab Adv Mat,Joint Key Lab Adv Ma, Shanghai 200237, Peoples R China
来源
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Nanopipettes; Cell-substrate; Cell membrane; Mechanical status; Single-cell; FUNCTIONAL-GROUPS; SURFACE-CHEMISTRY; ADHESION; DIFFERENTIATION; MICROSCOPY;
D O I
10.1016/j.bios.2024.116385
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Cell -substrate interaction plays a critical role in determining the mechanical status of living cell membrane. Changes of substrate surface properties can significantly alter the cell mechanical microenvironment, leading to mechanical changes of cell membrane. However, it is still difficult to accurately quantify the influence of the substrate surface properties on the mechanical status of living cell membrane without damage. This study addresses the challenge by using an electrochemical sensor made from an ultrasmall quartz nanopipette. With the tip diameter less than 100 nm, the nanopipette-based sensor achieves highly sensitive, noninvasive and label -free monitoring of the mechanical status of single living cells by collecting stable cyclic membrane oscillatory signals from continuous current versus time traces. The electrochemical signals collected from PC12 cells cultured on three different substrates (bare ITO (indium tin oxides) glass, hydroxyl modified ITO glass, amino modified ITO glass) indicate that the microenvironment more favorable for cell adhesion can increase the membrane stiffness. This work provides a label -free electrochemical approach to accurately quantify the mechanical status of single living cells in real-time, which may help to better understand the relationship between the cell membrane and the extra cellular matrix.
引用
收藏
页数:10
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