| Literature DB >> 25450003 |
Yi Yao1, Rebecca Liu2, Min Sun Shin1, Mark Trentalange1, Heather Allore1, Ala Nassar1, Insoo Kang1, Jordan S Pober3, Ruth R Montgomery4.
Abstract
Analysis of immune cell states is paramount to our understanding of the pathogenesis of a broad range of human diseases. Immunologists rely on fluorescence cytometry for cellular analysis, and while detection of 8 markers is now well established, the overlap of fluorescent signals limits efficiency. Mass cytometry or CyTOF (Cytometry by Time-Of-Flight) is a new technology for multiparameter single cell analysis that overcomes many limitations of fluorescence-based flow cytometry and can routinely detect as many as 40 markers per sample. This technology provides tremendous detail for cellular analysis of multiple cell populations simultaneously and is a powerful technique for translational investigations. Here we present reproducible detection of immune cell subsets starting with as few as 10,000 cells. Our study provides methods to employ CyTOF for small samples, which is especially relevant for investigation of limited patient biopsies in translational and clinical research.Entities:
Keywords: CyTOF; Leukocytes; Mass cytometry; Multidimensional single cell analysis; Translational immunology; Translational research
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Year: 2014 PMID: 25450003 PMCID: PMC4269324 DOI: 10.1016/j.jim.2014.10.010
Source DB: PubMed Journal: J Immunol Methods ISSN: 0022-1759 Impact factor: 2.303