OMIP-048 MC: Quantification of calcium sensors and channels expression in lymphocyte subsets by mass cytometry

Cytometry A. 2018 Jul;93(7):681-684. doi: 10.1002/cyto.a.23504. Epub 2018 Aug 6.

Abstract

Calcium (Ca2+ ) signaling controls T-cell activation and functions. Ca2+ concentrations are locally detected and controlled by Ca2+ -sensors (STIM1 and 2 detecting the depletion from ER stores channels) and Ca2+ -channels (ORAI1-3 in the cell membrane and VDAC1 in the outer mitochondrial membrane). We first validated and titrated antibodies to assess the expression of these Ca2+ -sensors and -channels in human and murine cells, and further devised a 18-antibodies mass cytometry panel to characterize their expression in primary murine lymphocyte subsets.

Keywords: calcium release-activated calcium channels (CRAC/ORAI); mass cytometry; murine primary lymphocyte subsets; panel design; stromal interaction molecule (STIM); voltage-dependent anion-selective channel protein (VDAC).

MeSH terms

  • Animals
  • Calcium Channels / genetics
  • Calcium Channels / isolation & purification*
  • Cell Membrane / genetics
  • Cell Membrane / metabolism
  • Flow Cytometry / methods*
  • Gene Expression Regulation / genetics*
  • Humans
  • Lymphocyte Subsets / immunology
  • Lymphocyte Subsets / metabolism
  • Mice
  • Mitochondrial Membranes / metabolism
  • ORAI1 Protein / genetics
  • ORAI1 Protein / isolation & purification
  • Stromal Interaction Molecule 1 / genetics
  • Stromal Interaction Molecule 1 / isolation & purification
  • Stromal Interaction Molecule 2 / genetics
  • Stromal Interaction Molecule 2 / isolation & purification
  • Voltage-Dependent Anion Channel 1 / genetics

Substances

  • Calcium Channels
  • ORAI1 Protein
  • Stromal Interaction Molecule 1
  • Stromal Interaction Molecule 2
  • Voltage-Dependent Anion Channel 1