Multiomics Characterization of a Less Invasive Microfluidic-Based Cell Sorting Technique

J Proteome Res. 2024 Aug 2;23(8):3096-3107. doi: 10.1021/acs.jproteome.3c00773. Epub 2024 Feb 28.

Abstract

Fluorescence-activated cell sorting (FACS) is a specialized technique to isolate specific cell subpopulations with a high level of recovery and accuracy. However, the cell sorting procedure can impact the viability and metabolic state of cells. Here, we performed a comparative study and evaluated the impact of traditional high-pressure charged droplet-based and microfluidic chip-based sorting on the metabolic and phosphoproteomic profile of different cell types. While microfluidic chip-based sorted cells more closely resembled the unsorted control group for most cell types tested, the droplet-based sorted cells showed significant metabolic and phosphoproteomic alterations. In particular, greater changes in redox and energy status were present in cells sorted with the droplet-based cell sorter along with larger shifts in proteostasis. 13C-isotope tracing analysis on cells recovering postsorting revealed that the sorter-induced suppression of mitochondrial TCA cycle activity recovered faster in the microfluidic chip-based sorted group. Apart from this, amino acid and lipid biosynthesis pathways were suppressed in sorted cells, with minimum impact and faster recovery in the microfluidic chip-based sorted group. These results indicate microfluidic chip-based sorting has a minimum impact on metabolism and is less disruptive compared to droplet-based sorting.

Keywords: LC-MS; Sorting; fluorescence-activated cell sorting (FACS); metabolomics; multiomics; phosphoproteomics; sorted cells; sorter-induced cellular stress (SICS); stable isotope tracing.

MeSH terms

  • Animals
  • Cell Separation / methods
  • Citric Acid Cycle
  • Flow Cytometry* / methods
  • Humans
  • Lab-On-A-Chip Devices
  • Microfluidic Analytical Techniques / instrumentation
  • Microfluidic Analytical Techniques / methods
  • Microfluidics / methods
  • Multiomics*
  • Proteomics / methods