The role of thrombin-activatable fibrinolysis inhibitor in diabetic wound healing

• Published in: Thrombosis research 2010-11, Vol.126 (5), p.442-446
• Main Authors: Verkleij, Chantal J.N, Roelofs, Joris J.T.H, Havik, Stefan R, Meijers, Joost C.M, Marx, Pauline F
• Format: Article
• Language: English
• Subjects: Animals; Associated diseases and complications; Biological and medical sciences; Blood and lymphatic vessels; Carboxypeptidase B2 - blood; Cardiology. Vascular system; Diabetes mellitus; Diabetes Mellitus - blood; Diabetes Mellitus - pathology; Diabetes. Impaired glucose tolerance; Disease Models, Animal; Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous; Endocrine pancreas. Apud cells (diseases); Endocrinopathies; Fibrinolysis; Hematology, Oncology and Palliative Medicine; Hyperglycaemia; Hyperglycemia - blood; Hyperglycemia - pathology; Medical sciences; Mice; Mice, Inbred C57BL; TAFI; Wound Healing
• ISSN: 0049-3848; 1879-2472
• DOI: 10.1016/j.thromres.2010.08.008

Abstract Introduction One of the major complications in patients with diabetes mellitus is impaired wound healing. The fibrinolytic system is involved in parts of the wound healing process and deficiency of thrombin-activatable fibrinolysis inhibitor (TAFI) results in delayed wound closure. Moreover, levels of TAFI are affected by diabetes mellitus. The aim of this study was to elucidate the effect of hyperglycaemia on TAFI and to determine the effect of deficiency of TAFI on wound healing under hyperglycaemic conditions. Materials and methods Hyperglycaemia was induced with streptozotocin (STZ) and used as a model for diabetes mellitus. TAFI plasma levels and TAFI gene expression in the liver were determined. Incisional and excisional wound healing were studied in non-treated and STZ-treated wild-type and TAFI-deficient mice. Wound closure was scored daily as open or closed. Results Mice treated with STZ showed hyperglycaemia, and TAFI plasma levels and TAFI gene expression were increased in diabetic mice. TAFI-deficient mice and diabetic wild-type and diabetic TAFI-deficient mice showed delayed wound healing of incisional wounds. No differences were observed between diabetic and non-diabetic TAFI-deficient mice and between diabetic wild-type and diabetic TAFI-deficient mice. Conclusions This study illustrated that TAFI was affected by hyperglycaemia and confirmed that TAFI is involved in wound healing. No additional effect was observed under hyperglycaemic conditions, indicating that deficiency of TAFI did not have an additive or synergistic effect in diabetic wound healing. Further research has to elucidate if TAFI and hyperglycemia affect wound healing via similar mechanisms.