The phospholipolytically active neurotoxin Vipoxin induces changes of the mechanical properties of breast epithelial cells

IF 2.8 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Will Linthicum , Qi Wen , Nancy A. Burnham , Svetla D. Petrova , Konstantin Balashev
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引用次数: 0

Abstract

The investigation of how drugs or toxins alter cell mechanics is gaining significant traction in biomedical science, driven by the dual objectives of elucidating their mechanisms of action and enhancing drug screening processes. In this study, Atomic Force Microscopy (AFM), a prominent experimental technique in recent years, was employed to examine and analyze the mechanical responses of cells exposed to the neurotoxin Vipoxin. This method enables the precise measurement of key mechanical parameters such as cell stiffness and viscoelasticity before and after toxin introduction in the cell culture. It was demonstrated that the cells' stiffness and viscosity decreased with increasing Vipoxin concentration. Additionally, Total Internal Reflection Fluorescence Microscopy (TIRFM) was utilized to monitor morphological changes in the cells over time. These morphological changes were quantitatively analyzed using fractal analysis of the acquired images. The observed changes in cell shapes implied the reorganization of the cell cytoskeleton, thus providing insight into a comprehensive understanding of cell mechanics under the influence of Vipoxin.

Abstract Image

磷脂多活性神经毒素Vipoxin诱导乳腺上皮细胞力学特性的改变。
在阐明其作用机制和加强药物筛选过程的双重目标的驱动下,药物或毒素如何改变细胞力学的研究在生物医学科学中获得了显著的吸引力。在本研究中,原子力显微镜(AFM)是近年来一项重要的实验技术,用于检测和分析细胞暴露于神经毒素Vipoxin的力学反应。该方法能够在细胞培养中引入毒素前后精确测量细胞刚度和粘弹性等关键力学参数。结果表明,随着Vipoxin浓度的增加,细胞的刚度和黏度降低。此外,利用全内反射荧光显微镜(TIRFM)监测细胞随时间的形态学变化。这些形态变化是定量分析使用分形分析获得的图像。观察到的细胞形状的变化暗示了细胞骨架的重组,从而为全面了解Vipoxin影响下的细胞力学提供了见解。
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来源期刊
Biochimica et biophysica acta. Biomembranes
Biochimica et biophysica acta. Biomembranes 生物-生化与分子生物学
CiteScore
8.20
自引率
5.90%
发文量
175
审稿时长
2.3 months
期刊介绍: BBA Biomembranes has its main focus on membrane structure, function and biomolecular organization, membrane proteins, receptors, channels and anchors, fluidity and composition, model membranes and liposomes, membrane surface studies and ligand interactions, transport studies, and membrane dynamics.
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