Phosphoflow cytometry and barcoding in blood platelets: Technical and analytical considerations

Cytometry B Clin Cytom. 2020 Mar;98(2):123-130. doi: 10.1002/cyto.b.21851. Epub 2019 Nov 1.

Abstract

Platelet function is regulated by finely tuned phosphoprotein signals. Subtle aberrations in signaling can cause platelet hyperactivity and severe cardiovascular events. Mapping phosphorylation profiles in health and disease could accelerate antiplatelet discovery and enhance cardiovascular management, but traditional assays are ill-suited to clinical application as they are laborious and low throughput. Recent advances in multiplex flow cytometry (barcoding) allow the rapid acquisition of highly batched samples with standard laboratory equipment. However, many assays have not been standardized, and success is largely dependent on protocol/reagent selection. Accordingly, we review the technical steps that are key to success with an emphasis on fixation, permeabilization, staining, controls, and data visualization.

Keywords: blood platelets; cardiovascular diseases; flow cytometry; phosphorylation; platelet function tests.

Publication types

  • Review

MeSH terms

  • Blood Platelets / chemistry
  • Blood Platelets / cytology
  • Blood Platelets / metabolism*
  • Flow Cytometry / methods*
  • Flow Cytometry / standards
  • Metabolome
  • Metabolomics / methods
  • Metabolomics / standards
  • Phosphoproteins / analysis
  • Phosphoproteins / metabolism*
  • Phosphorylation / physiology
  • Phosphotransferases / metabolism
  • Protein Processing, Post-Translational
  • Proteomics / methods
  • Proteomics / standards
  • Quality Control
  • Staining and Labeling / methods
  • Staining and Labeling / standards

Substances

  • Phosphoproteins
  • Phosphotransferases