Flow cytometry analysis reveals different activation profiles of thrombin- or TRAP-stimulated platelets in db/db mice. The regulatory role of PAR-3

Blood Cells Mol Dis. 2017 Jun:65:16-22. doi: 10.1016/j.bcmd.2017.03.011. Epub 2017 Mar 22.

Abstract

Introduction: Recent studies have shown that it may be the concentration of thrombin, which is discriminative in determining of the mechanism of platelet activation via protease activated receptors (PARs). Whether the observed phenomenon of differentiated responses of mouse platelets to various thrombin concentrations in non-diabetic db/+ and diabetic db/db mice depends upon the concerted action of various PARs, remains to be established.

Results: We found elevated reactivity of platelets, as well as the enhanced PAR-3 expression in response to both the used concentrations of AYPGKF in db/db mice, as compared to db/+ heterozygotes. At low concentration of thrombin platelets from diabetic mice demonstrated hyperreactivity, reflected by higher expression of PAR-3. For higher thrombin concentration, blood platelets from db/db mice appeared hyporeactive, compared to db/+ animals, while no significant differences in PAR-3 expression were observed between diabetic and non-diabetic mice.

Conclusions: The novel and previously unreported finding resulting from our study is that the increased expression of PAR-3 in response to either TRAP for PAR-4 or low thrombin (when PAR-4 is not the efficient thrombin receptor) may be one of the key events contributing to higher reactivity of platelets in db/db mice.

Keywords: Diabetes; Flow cytometry; PARs; Platelets; db/db mice.

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • Biomarkers
  • Blood Platelets / drug effects
  • Blood Platelets / metabolism*
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism*
  • Cell Cycle Proteins
  • Diabetes Mellitus, Experimental / blood
  • Diabetes Mellitus, Experimental / genetics
  • Diabetes Mellitus, Experimental / metabolism
  • Flow Cytometry
  • Gene Expression
  • Male
  • Mice
  • Oligopeptides / pharmacology
  • Platelet Activation* / drug effects
  • Platelet Activation* / genetics
  • Tartrate-Resistant Acid Phosphatase / metabolism*
  • Thrombin / metabolism*

Substances

  • Adaptor Proteins, Signal Transducing
  • Biomarkers
  • Cell Adhesion Molecules
  • Cell Cycle Proteins
  • Oligopeptides
  • Pard3 protein, mouse
  • alanyl-tyrosyl-prolyl-glycyl-lysyl-phenylalanine
  • Tartrate-Resistant Acid Phosphatase
  • Thrombin