Pim Kinase Inhibition Disrupts CXCR4 Signalling in Megakaryocytes and Platelets by Reducing Receptor Availability at the Surface

Int J Mol Sci. 2024 Jul 11;25(14):7606. doi: 10.3390/ijms25147606.

Abstract

A key step in platelet production is the migration of megakaryocytes to the vascular sinusoids within the bone marrow. This homing is mediated by the chemokine CXCL12 and its receptor CXCR4. CXCR4 is also a positive regulator of platelet activation and thrombosis. Pim-1 kinase has been shown to regulate CXCR4 signalling in other cell types, and we have previously described how Pim kinase inhibitors attenuate platelet aggregation to CXCL12. However, the mechanism by which Pim-1 regulates CXCR4 signalling in platelets and megakaryocytes has yet to be elucidated. Using human platelets, murine bone marrow-derived megakaryocytes, and the megakaryocyte cell line MEG-01, we demonstrate that pharmacological Pim kinase inhibition leads to reduced megakaryocyte and platelet function responses to CXCL12, including reduced megakaryocyte migration and platelet granule secretion. Attenuation of CXCL12 signalling was found to be attributed to the reduced surface expression of CXCR4. The decrease in CXCR4 surface levels was found to be mediated by rapid receptor internalisation, in the absence of agonist stimulation. We demonstrate that pharmacological Pim kinase inhibition disrupts megakaryocyte and platelet function by reducing constitutive CXCR4 surface expression, decreasing the number of receptors available for agonist stimulation and signalling. These findings have implications for the development and use of Pim kinase inhibitors for the treatment of conditions associated with elevated circulating levels of CXCL12/SDF1α and increased thrombotic risk.

Keywords: CXCL12/SDF1α; CXCR4; GPCR; Pim kinase; megakaryocytes; platelets; signalling; thrombopoiesis.

MeSH terms

  • Animals
  • Blood Platelets* / drug effects
  • Blood Platelets* / metabolism
  • Cell Line
  • Cell Movement / drug effects
  • Chemokine CXCL12* / metabolism
  • Humans
  • Megakaryocytes* / cytology
  • Megakaryocytes* / drug effects
  • Megakaryocytes* / metabolism
  • Mice
  • Protein Kinase Inhibitors / pharmacology
  • Proto-Oncogene Proteins c-pim-1* / antagonists & inhibitors
  • Proto-Oncogene Proteins c-pim-1* / metabolism
  • Receptors, CXCR4* / metabolism
  • Signal Transduction* / drug effects

Substances

  • Receptors, CXCR4
  • Proto-Oncogene Proteins c-pim-1
  • Chemokine CXCL12
  • CXCR4 protein, human
  • Protein Kinase Inhibitors