| Literature DB >> 30536717 |
Ning Ma1,2,3, Gopakumar Kamalakshakurup1,3, Mohammad Aghaamoo1, Abraham P Lee1,3,4, Michelle A Digman1,2,3.
Abstract
Characterization of single cell metabolism is imperative for understanding subcellular functional and biochemical changes associated with healthy tissue development and the progression of numerous diseases. However, single-cell analysis often requires the use of fluorescent tags and cell lysis followed by genomic profiling to identify the cellular heterogeneity. Identifying individual cells in a noninvasive and label-free manner is crucial for the detection of energy metabolism which will discriminate cell types and most importantly critical for maintaining cell viability for further analysis. Here, we have developed a robust assay using the droplet microfluidic technology together with the phasor approach to fluorescence lifetime imaging microscopy to study cell heterogeneity within and among the leukemia cell lines (K-562 and Jurkat). We have extended these techniques to characterize metabolic differences between proliferating and quiescent cells-a critical step toward label-free single cancer cell dormancy research. The result suggests a droplet-based noninvasive and label-free method to distinguish individual cells based on their metabolic states, which could be used as an upstream phenotypic platform to correlate with genomic statistics.Entities:
Keywords: circulating tumor cells; droplet microfluidics; fluorescence lifetime imaging microscopy; metabolism; phasor analysis; quiescent stage; single cell analysis
Year: 2018 PMID: 30536717 PMCID: PMC6613543 DOI: 10.1002/cyto.a.23673
Source DB: PubMed Journal: Cytometry A ISSN: 1552-4922 Impact factor: 4.355