Platelet-Derived TGF-β1 Promotes Deep Vein Thrombosis

Thromb Haemost. 2024 Jul;124(7):641-648. doi: 10.1055/a-2235-7485. Epub 2023 Dec 27.

Abstract

Background: Transforming growth factor-β1 (TGF-β1) modulates multiple cellular functions during development and tissue homeostasis. A large amount of TGF-β1 is stored in platelet α-granules and released upon platelet activation. Whether platelet-derived TGF-β1 plays a role in venous thrombosis remains unclear. This study intends to assess the role of platelet-derived TGF-β1 in the development of venous thrombosis in mice.

Material and methods: TGF-β1flox/flox and platelet-specific TGF-β1-/- mice were utilized to assess platelet function in vitro, arterial thrombosis induced by FeCl3, tail bleeding time, prothrombin time (PT), activated partial thromboplastin time (APTT), and deep vein thrombosis induced through ligation of the inferior vena cava (IVC). The IVC sample was collected to measure accumulation of neutrophils, monocytes, and the formation of neutrophil extracellular traps (NETs) by immunofluorescence staining.

Results: TGF-β1 deficiency in platelets did not affect the number of circulating platelets, platelet aggregation, adenosine triphosphate release, and integrin αIIbβ3 activation. Meanwhile, TGF-β1 deficiency did not alter the arterial thrombus formation, hemostasis, and coagulation time (PT and APTT), but significantly impaired venous thrombus formation, inhibited the recruitment and accumulation of neutrophils and monocytes in thrombi, as well as reduced formation of NETs and platelet-neutrophil complex. In addition, adoptive transfer of TGF-β1flox/flox platelets to TGF-β1-/- mice rescued the impaired venous thrombus formation, recruitment of leukocytes and monocytes, as well as the NETs formation.

Conclusion: In conclusion, platelet-derived TGF-β1 positively modulates venous thrombus formation in mice, indicating that targeting TGF-β1 might be a novel approach for treating venous thrombosis without increasing the risk of bleeding.

MeSH terms

  • Animals
  • Blood Coagulation
  • Blood Platelets* / metabolism
  • Disease Models, Animal
  • Extracellular Traps / metabolism
  • Hemostasis
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout*
  • Neutrophils / metabolism
  • Platelet Activation
  • Platelet Aggregation
  • Transforming Growth Factor beta1* / metabolism
  • Vena Cava, Inferior / metabolism
  • Vena Cava, Inferior / pathology
  • Venous Thrombosis* / blood
  • Venous Thrombosis* / metabolism

Substances

  • Transforming Growth Factor beta1
  • Tgfb1 protein, mouse