SLC44A2 deficient mice have a reduced response in stenosis but not in hypercoagulability driven venous thrombosis

J Thromb Haemost. 2020 Jul;18(7):1714-1727. doi: 10.1111/jth.14835. Epub 2020 May 15.

Abstract

Background: Genome wide association studies (GWAS) identified SLC44A2 as a novel susceptibility gene for venous thrombosis (VT) and previous work established that SLC44A2 contributed to clot formation upon vascular injury.

Objective: To further investigate the role of SLC44A2 in VT by utilizing SLC44A2 deficient mice (Slc44a2-/- ) in two representative disease models.

Methods: Mice were included in a hypercoagulability model driven by siRNA-mediated hepatic gene silencing of anticoagulants Serpinc1 (antithrombin) and Proc (protein C) and a flow restriction (stenosis) model induced by partial ligation of the inferior vena cava.

Results: In the hypercoagulability model, no effect in onset was observed in Slc44a2-/- animals; however, a drop in plasma fibrinogen and von Willebrand factor coinciding with an increase in blood neutrophils was recorded. In the neutrophil dependent stenosis model after 48 hours, Slc44a2-/- mice had significantly smaller thrombi both in length and weight with less platelet accumulation as a percentage of the total thrombus area. During the initiation of thrombosis at 6 hours post-stenosis, Slc44a2-/- mice also had smaller thrombi both in length and weight, with circulating platelets remaining elevated in Slc44a2-/- animals. Platelet activation and aggregation under both static- and venous and arterial shear conditions were normal for blood from Slc44a2-/- mice.

Conclusions: These studies corroborate the original GWAS findings and establish a contributing role for SLC44A2 during the initiation of VT, with indications that this may be related to platelet-neutrophil interaction. The precise mechanism however remains elusive and warrants further investigation.

Keywords: animal models of human disease; basic science research; thrombosis; vascular biology; vascular diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Platelets
  • Constriction, Pathologic
  • Disease Models, Animal
  • Genome-Wide Association Study
  • Membrane Transport Proteins / genetics
  • Mice
  • Platelet Activation
  • Thrombophilia* / genetics
  • Venous Thrombosis* / genetics

Substances

  • Membrane Transport Proteins
  • SLC44A2 protein, mouse