Analysis of preplatelets and their barbell platelet derivatives by imaging flow cytometry.
Samuel KembleAmanda DalbyGillian C LowePhillip Lindsay Ross NicolsonStephen P WatsonYotis A SenisSteven G ThomasPaul HarrisonPublished in: Blood advances (2022)
Circulating large "preplatelets" undergo fission via barbell platelet intermediates into two smaller, mature platelets. In this study, we determine whether preplatelets and/or barbells are equivalent to reticulated/immature platelets by using ImageStream flow cytometry and super-resolution microscopy. Immature platelets, preplatelets, and barbells were quantified in healthy and thrombocytopenic mice, healthy human volunteers, and patients with immune thrombocytopenia or undergoing chemotherapy. Preplatelets and barbells were 1.9% ± 0.18%/1.7% ± 0.48% (n = 6) and 3.3% ± 1.6%/0.5% ± 0.27% (n = 12) of total platelet counts in murine and human whole blood, respectively. Both preplatelets and barbells exhibited high expression of major histocompatibility complex class I with high thiazole orange and Mitotracker fluorescence. Tracking dye experiments confirmed that preplatelets transform into barbells and undergo fission ex vivo to increase platelet counts, with dependence on the cytoskeleton and normal mitochondrial respiration. Samples from antibody-induced thrombocytopenia in mice and patients with immune thrombocytopenia had increased levels of both preplatelets and barbells correlating with immature platelet levels. Furthermore, barbells were absent after chemotherapy in patients. In mice, in vivo biotinylation confirmed that barbells, but not all large platelets, were immature. This study demonstrates that a subpopulation of large platelets are immature preplatelets that can transform into barbells and undergo fission during maturation.
Keyphrases
- flow cytometry
- endothelial cells
- high fat diet induced
- high resolution
- ejection fraction
- single molecule
- squamous cell carcinoma
- peripheral blood
- prognostic factors
- locally advanced
- adipose tissue
- high throughput
- chronic kidney disease
- long non coding rna
- type diabetes
- patient reported outcomes
- diabetic rats
- binding protein
- mass spectrometry
- high speed