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使用量子点探针测量细胞运动性。

Measuring cell motility using quantum dot probes.

作者信息

Gu Weiwei, Pellegrino Teresa, Parak Wolfgang J, Boudreau Rosanne, Le Gros Mark A, Alivisatos A Paul, Larabell Carolyn A

机构信息

Department of Anatomy, University of California, San Francisco, CA, USA.

出版信息

Methods Mol Biol. 2007;374:125-31. doi: 10.1385/1-59745-369-2:125.

Abstract

The ability of cancer cells to migrate and metastasize is known to be directly related to tumor cell motility. Therefore, assaying the level of tumor cell motility is an excellent indicator of metastatic potential. We have developed an efficient and sensitive two-dimensional cell motility assay to image the phagokinetic uptake of colloidal CdSe/ZnS semiconductor nanocrystals (quantum dots [QDs]). As cells move across a thin, homogeneous layer of QDs, they engulf and uptake the nanocrystals and leave behind a fluorescent-free trail. By measuring the ratio of trail area to cell area we have discovered that it is possible to distinguish between noninvasive and invasive cancer cells lines. This technique has, therefore, the potential to be used as a rapid, robust, and quantitative in vitro measure of metastatic potential. Because the technique only relies on fluorescence detection, requires no significant data processing, and is used with live cells, it is both rapid and straightforward.

摘要

已知癌细胞迁移和转移的能力与肿瘤细胞的运动性直接相关。因此,检测肿瘤细胞的运动水平是转移潜能的一个极佳指标。我们开发了一种高效且灵敏的二维细胞运动检测方法,用于成像胶体CdSe/ZnS半导体纳米晶体(量子点[QDs])的吞噬动力学摄取。当细胞在一层薄薄的、均匀的量子点上移动时,它们会吞噬并摄取纳米晶体,留下一条无荧光的轨迹。通过测量轨迹面积与细胞面积的比值,我们发现能够区分非侵袭性和侵袭性癌细胞系。因此,这项技术有潜力用作一种快速、可靠且定量的体外转移潜能检测方法。由于该技术仅依赖荧光检测,无需大量数据处理,且用于活细胞,所以既快速又简便。

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