Functional Analysis of the Fibrinogen Aα Thr312Ala Polymorphism
- 13 May 2003
- journal article
- research article
- Published by Wolters Kluwer Health in Circulation
- Vol. 107 (18) , 2326-2330
- https://doi.org/10.1161/01.cir.0000066690.89407.ce
Abstract
Background— The fibrinogen Aα Thr312Ala polymorphism occurs within the αC domain of fibrinogen, which is important for lateral aggregation and factor XIII-induced cross-linking of fibrin fibers. We have previously shown an association of Ala312 fibrinogen with poststroke mortality in subjects with atrial fibrillation and with pulmonary embolism in subjects with venous thrombosis. Methods and Results— We studied the properties of clots formed from purified Ala312 and Thr312 fibrinogen and found that Ala312 fibrinogen produces stiffer clots, associated with increased α chain cross-linking, as demonstrated by SDS-Page. On electron microscopy analysis, we found larger fiber diameters in the Ala312 clots and observed a lower number of fibers per square micrometer. The number of branch points per square micrometer was similar between genotypes. Conclusions— Our study shows that Ala312 influences clot structure and properties by increased factor XIII cross-linking and formation of thicker fibrin fibers. These fi...Keywords
This publication has 16 references indexed in Scilit:
- Altered Fibrin Clot Structure in the Healthy Relatives of Patients With Premature Coronary Artery DiseaseCirculation, 2002
- The Effect of Dimethylbiguanide on Thrombin Activity, FXIII Activation, Fibrin Polymerization, and Fibrin Clot FormationDiabetes, 2002
- The Structure and Function of the αC Domains of FibrinogenAnnals of the New York Academy of Sciences, 2001
- Structural Origins of Fibrin Clot RheologyBiophysical Journal, 1999
- The Ultrastructure of Fibrinogen Caracas II Molecules, Fibers, and ClotsPublished by Elsevier ,1996
- Proneness to Formation of Tight and Rigid Fibrin Gel Structures in Men with Myocardial Infarction at a Young AgeThrombosis and Haemostasis, 1996
- Novel Aspects of Blood Coagulation Factor XIII. I. Structure, Distribution, Activation, and FunctionCritical Reviews in Clinical Laboratory Sciences, 1996
- Native fibrin gel networks observed by 3D microscopy, permeation and turbidityBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1989
- HAEMOSTATIC FUNCTION AND ISCHAEMIC HEART DISEASE: PRINCIPAL RESULTS OF THE NORTHWICK PARK HEART STUDYThe Lancet, 1986
- .alpha.-Chain domain of fibrinogen controls generation of fibrinoligase (coagulation factor XIIIa). Calcium ion regulatory aspectsBiochemistry, 1981