Multiplexed Epitope-Based Tissue Imaging for Discovery and Healthcare Applications

被引:182
作者
Bodenmiller, Bernd [1 ]
机构
[1] Univ Zurich, Inst Mol Life Sci, CH-8057 Zurich, Switzerland
基金
欧洲研究理事会;
关键词
SINGLE-CELL ANALYSIS; MASS-SPECTROMETRY; EXPRESSION PATTERNS; ORGANOTYPIC CULTURE; PROTEIN EXPRESSION; TUMOR XENOGRAFTS; GENE-EXPRESSION; CYTOMETRY DATA; RNA-ANALYSIS; STEM-CELLS;
D O I
10.1016/j.cels.2016.03.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The study of organs and tissues on a molecular level is necessary as we seek an understanding of health and disease. Over the last few years, powerful highly multiplexed epitope-based imaging approaches that rely on the serial imaging of tissues with fluorescently labeled antibodies and the simultaneous analysis using metal-labeled antibodies have emerged. These techniques enable analysis of dozens of epitopes in thousands of cells in a single experiment providing a systems level view of normal and disease processes at the single-cell level with spatial resolution in tissues. In this Review, I discuss, first, the highly multiplexed epitope-based imaging approaches and the generated data. Second, I describe challenges that must be overcome to implement these imaging methods from bench to bedside, including issues with tissue processing and analyses of the large amounts of data generated. Third, I discuss how these methods can be integrated with readouts of genome, transcriptome, metabolome, and live cell information, and fourth, the novel applications possible in tissue biology, drug development, and biomarker discovery. I anticipate that highly multiplexed epitope-based imaging approaches will broadly complement existing imaging methods and will become a cornerstone of tissue biology and biomedical research and of precision medical applications.
引用
收藏
页码:225 / 238
页数:14
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