Cystamine Preparations Exhibit Anticoagulant Activity

Transglutaminases are a superfamily of isoenzymes found in cells and plasma. These enzymes catalyze the formation of ε-N-(γ-glutamyl)-lysyl crosslinks between proteins. Cystamine blocks transglutaminase activity and is used in vitro in human samples and in vivo in mice and rats in studies of coagulation, immune dysfunction, and inflammatory disease. These studies have suggested cystamine blocks fibrin crosslinking and has anti-inflammatory effects, implicating transglutaminase activity in the pathogenesis of several diseases. We measured the effects of cystamine on fibrin crosslinking, tissue factor-triggered plasma clot formation and thrombin generation, and coagulation factor enzymatic activity. At concentrations that blocked fibrin crosslinking, cystamine also inhibited plasma clot formation and reduced thrombin generation. Cystamine inhibited the amidolytic activity of coagulation factor XI and thrombin towards chromogenic substrates. These findings demonstrate that cystamine exhibits anticoagulant activity during coagulation. Given the close relationship between coagulation and inflammation, these findings suggest prior studies that used cystamine to implicate transglutaminase activity in disease pathogenesis warrant re-examination.

[1]  E. Mullins,et al.  Transglutaminase factor XIII promotes arthritis through mechanisms linked to inflammation and bone erosion. , 2015, Blood.

[2]  W. Lam,et al.  Factor XIII activity mediates red blood cell retention in venous thrombi. , 2014, Journal of Clinical Investigation.

[3]  Zi Li,et al.  Involvement of IL-13 and Tissue Transglutaminase in Liver Granuloma and Fibrosis after Schistosoma japonicum Infection , 2014, Mediators of inflammation.

[4]  A. Wolberg,et al.  Abnormal plasma clot structure and stability distinguish bleeding risk in patients with severe factor XI deficiency , 2014, Journal of thrombosis and haemostasis : JTH.

[5]  B. Sibai,et al.  Tissue Transglutaminase Contributes to the Pathogenesis of Preeclampsia and Stabilizes Placental Angiotensin Receptor Type 1 by Ubiquitination-Preventing Isopeptide Modification , 2014, Hypertension.

[6]  A. Rego,et al.  Oxidizing effects of exogenous stressors in Huntington's disease knock-in striatal cells--protective effect of cystamine and creatine. , 2013, Toxicological sciences : an official journal of the Society of Toxicology.

[7]  M. Maiuri,et al.  Towards a rational combination therapy of cystic fibrosis , 2013, Autophagy.

[8]  J. Levy,et al.  Biology of Factor XIII and clinical manifestations of Factor XIII deficiency , 2013, Transfusion.

[9]  B. Tzang,et al.  Cystamine ameliorates ventricular hypertrophy associated with modulation of IL-6-mediated signaling in lupus-prone mice. , 2013, Life sciences.

[10]  I. Lavi,et al.  The thrombophilic network of autoantibodies in celiac disease , 2013, BMC Medicine.

[11]  M. Bardella,et al.  Beneficial effects of treatment with transglutaminase inhibitor cystamine on the severity of inflammation in a rat model of inflammatory bowel disease , 2011, Laboratory Investigation.

[12]  A. Messer,et al.  Cystamine and intrabody co-treatment confers additional benefits in a fly model of Huntington's disease , 2010, Neurobiology of Disease.

[13]  A. Ichinose,et al.  Impaired clot retraction in factor XIII A subunit-deficient mice. , 2010, Blood.

[14]  N. Key,et al.  Effects of tissue factor, thrombomodulin and elevated clotting factor levels on thrombin generation in the calibrated automated thrombogram , 2009, Thrombosis and Haemostasis.

[15]  B. Tzang,et al.  Beneficial effects of treatment with cystamine on brain in NZB/W F1 mice. , 2008, European journal of pharmacology.

[16]  T. Luther,et al.  Protease-Activated Receptor-1 Contributes to Cardiac Remodeling and Hypertrophy , 2007, Circulation.

[17]  Alisa S Wolberg,et al.  Thrombin generation and fibrin clot structure. , 2007, Blood reviews.

[18]  Adrian Pistea,et al.  Flow-Dependent Remodeling of Small Arteries in Mice Deficient for Tissue-Type Transglutaminase: Possible Compensation by Macrophage-Derived Factor XIII , 2006, Circulation research.

[19]  G. Johnson,et al.  The protective effects of cystamine in the R6/2 Huntington's disease mouse involve mechanisms other than the inhibition of tissue transglutaminase , 2006, Neurobiology of Aging.

[20]  E. Hirsch,et al.  Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase. , 2006, The Journal of clinical investigation.

[21]  J. Loscalzo,et al.  Factor XIII (FXIII) and angiogenesis , 2006, Journal of thrombosis and haemostasis : JTH.

[22]  M. Hayden,et al.  Cystamine treatment is neuroprotective in the YAC128 mouse model of Huntington disease , 2005, Journal of neurochemistry.

[23]  Jop Perree,et al.  Small Artery Remodeling Depends on Tissue-Type Transglutaminase , 2004, Circulation research.

[24]  Sawsan Youssef,et al.  Prolonged survival and decreased abnormal movements in transgenic model of Huntington disease, with administration of the transglutaminase inhibitor cystamine , 2002, Nature Medicine.

[25]  G. Kirdaitė,et al.  Amelioration of collagen-induced arthritis by thrombin inhibition. , 2001, The Journal of clinical investigation.

[26]  P. Varisco,et al.  Effect of thrombin inhibition on synovial inflammation in antigen induced arthritis , 2000, Annals of the rheumatic diseases.

[27]  D. Schuppan,et al.  Identification of tissue transglutaminase as the autoantigen of celiac disease , 1997, Nature Medicine.

[28]  D. Speicher,et al.  Complete amino acid sequence and homologies of human erythrocyte membrane protein band 4.2. , 1990, Proceedings of the National Academy of Sciences of the United States of America.