Exploring cell structure, dynamics and homeostasis with a multimodal microscopy approach based on digital holographic microscopy: towards identifying early biomarkers of cell viability and cytotoxicity

P. Marquet, P. Jourdain, E. Bélanger, P. Magistretti
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引用次数: 1

Abstract

Among the different techniques in the growing field of quantitative phase imaging (QPI), Quantitative Phase Digital Holographic Microscopy (QP-DHM) is particularly well suited to explore, with a nanometric axial sensitivity, cell structure and dynamics, by providing quantitative phase signal (QPS). QPS depends on both the thickness and the intracellular refractive index of the observed cells and brings thus information about both cell morphology and cell contents. Thanks to the development of different experimental procedures, relevant biophysical cell parameters can be successfully calculated from QPS, including cell shape, absolute volume, intracellular protein concentration, organelle distribution, nanoscale membrane fluctuations, membrane mechanical properties and water permeability, as well as transmembrane water movements. Simultaneous dynamic imaging of transmembrane water movements and cell volume is likely to assess the cell capacity to maintain or not homeostasis and consequently to identify early biomarkers of cell viability and cytotoxicity.
利用基于数字全息显微镜的多模态显微镜方法探索细胞结构、动力学和稳态:识别细胞活力和细胞毒性的早期生物标志物
在不断发展的定量相位成像(QPI)领域的不同技术中,定量相位数字全息显微镜(QP-DHM)特别适合通过提供定量相位信号(QPS)来探索具有纳米轴向灵敏度的细胞结构和动力学。QPS依赖于被观察细胞的厚度和细胞内折射率,从而带来关于细胞形态和细胞含量的信息。由于不同实验方法的发展,从QPS中可以成功地计算出相关的生物物理细胞参数,包括细胞形状、绝对体积、细胞内蛋白质浓度、细胞器分布、纳米级膜波动、膜力学性能和水渗透性以及跨膜水运动。跨膜水运动和细胞体积的同时动态成像可能评估细胞维持或不维持稳态的能力,从而识别细胞活力和细胞毒性的早期生物标志物。
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