无创,无标记,单层培养活细胞的定量表征

Jing Zhang, D. Morris, V. Sottile, J. Crowe, M. Somekh, M. Mather
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引用次数: 0

摘要

细胞培养对生物学的许多领域都是必不可少的,从细胞生物学的基础研究到细胞在再生医学中的治疗应用。所有这些领域的共同点是需要描述培养下的细胞群。目前,细胞群的常规监测使用传统的生物分析,如细胞表面标记,基因表达。这种方法是破坏性的,不适合在过程中测量,使时间过程实验不可能。另外,也可以使用评估细胞形态的非破坏性方法,光学显微镜技术(例如,明场,相对比成像)是主要方法。这些显微镜技术有时可以结合使用外源标记,如荧光标记。这可以提供功能信息,但缺点是这种细胞修饰是侵入性的,对细胞有潜在的毒性。
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Non-invasive, label free, quantitative characterisation of live cells in monolayer culture
Cell culture is essential to many areas of biology ranging from the fundamental study of cell biology to the application of cells for therapeutic purposes in Regenerative Medicine. Common to all these areas is the need to characterise cell populations under culture. Currently, cell populations are routinely monitored using conventional biological analysis e.g. cell surface markers, gene expression. This approach is destructive, not suitable for in-process measurements and renders time course experiments impossible. Alternatively non-destructive approaches that assess cell morphology can also be used, with light microscopy techniques (e.g. bright field, phase contrast imaging) being the primary methods. These microscopy techniques can sometimes be combined with the use of exogenous labels such as fluorescent markers. This can provide functional information but has the disadvantage that such cell modifications are invasive and potentially toxic to the cells.
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