Multiplexed ion beam imaging of human breast tumors

被引:786
作者
Angelo, Michael [1 ,2 ]
Bendall, Sean C. [1 ]
Finck, Rachel [1 ]
Hale, Matthew B. [1 ]
Hitzman, Chuck [3 ]
Borowsky, Alexander D. [4 ]
Levenson, Richard M. [4 ]
Lowe, John B. [5 ]
Liu, Scot D. [5 ]
Zhao, Shuchun [6 ]
Natkunam, Yasodha [6 ]
Nolan, Garry P. [1 ]
机构
[1] Stanford Univ, Dept Microbiol & Immunol, Baxter Lab Stem Cell Biol, Stanford, CA 94305 USA
[2] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
[3] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[4] Univ Calif Davis, Dept Pathol & Lab Med, Sacramento, CA 95817 USA
[5] Genentech Inc, Dept Pathol, San Francisco, CA 94080 USA
[6] Stanford Univ, Dept Pathol, Stanford, CA 94305 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
MASS-SPECTROMETRY; PROTEIN EXPRESSION; CYTOMETRY; ANTIBODY; IMMUNOHISTOCHEMISTRY; QUANTIFICATION; CLUSTERS; TISSUES;
D O I
10.1038/nm.3488
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
Immunohistochemistry (IHC) is a tool for visualizing protein expression that is employed as part of the diagnostic workup for the majority of solid tissue malignancies. Existing IHC methods use antibodies tagged with fluorophores or enzyme reporters that generate colored pigments. Because these reporters exhibit spectral and spatial overlap when used simultaneously, multiplexed IHC is not routinely used in clinical settings. We have developed a method that uses secondary ion mass spectrometry to image antibodies tagged with isotopically pure elemental metal reporters. Multiplexed ion beam imaging (MIBI) is capable of analyzing up to 100 targets simultaneously over a five-log dynamic range. Here, we used MIBI to analyze formalin-fixed, paraffin-embedded human breast tumor tissue sections stained with ten labels simultaneously. The resulting data suggest that MIBI can provide new insights into disease pathogenesis that will be valuable for basic research, drug discovery and clinical diagnostics.
引用
收藏
页码:436 / +
页数:9
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