Document Detail


Structural origins of fibrin clot rheology.
MedLine Citation:
PMID:  10545379     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The origins of clot rheological behavior associated with network morphology and factor XIIIa-induced cross-linking were studied in fibrin clots. Network morphology was manipulated by varying the concentrations of fibrinogen, thrombin, and calcium ion, and cross-linking was controlled by a synthetic, active-center inhibitor of FXIIIa. Quantitative measurements of network features (fiber lengths, fiber diameters, and fiber and branching densities) were made by analyzing computerized three-dimensional models constructed from stereo pairs of scanning electron micrographs. Large fiber diameters and lengths were established only when branching was minimal, and increases in fiber length were generally associated with increases in fiber diameter. Junctions at which three fibers joined were the dominant branchpoint type. Viscoelastic properties of the clots were measured with a rheometer and were correlated with structural features of the networks. At constant fibrinogen but varying thrombin and calcium concentrations, maximal rigidities were established in samples (both cross-linked and noncross-linked) which displayed a balance between large fiber sizes and great branching. Clot rigidity was also enhanced by increasing fiber and branchpoint densities at greater fibrinogen concentrations. Network morphology is only minimally altered by the FXIIIa-catalyzed cross-linking reaction, which seems to augment clot rigidity most likely by the stiffening of existing fibers.
Authors:
E A Ryan; L F Mockros; J W Weisel; L Lorand
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural    
Journal Detail:
Title:  Biophysical journal     Volume:  77     ISSN:  1542-0086     ISO Abbreviation:  Biophys. J.     Publication Date:  1999 Nov 
Date Detail:
Created Date:  2010-08-30     Completed Date:  2010-12-03     Revised Date:  2012-05-07    
Medline Journal Info:
Nlm Unique ID:  0370626     Medline TA:  Biophys J     Country:  United States    
Other Details:
Languages:  eng     Pagination:  2813-26     Citation Subset:  IM    
Affiliation:
Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, Illinois 60611, USA.
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MeSH Terms
Descriptor/Qualifier:
Blood Coagulation* / drug effects
Calcium / metabolism
Electrophoresis, Polyacrylamide Gel
Factor XIIIa / antagonists & inhibitors
Fibrin / chemistry*,  metabolism*
Fibrinogen / chemistry,  metabolism
Humans
Imaging, Three-Dimensional
Imidazoles / pharmacology
Rheology* / drug effects
Thrombin / chemistry,  metabolism
Grant Support
ID/Acronym/Agency:
HL-02212/HL/NHLBI NIH HHS; HL-30954/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
0/Imidazoles; 134218-50-1/1,3,4,5-tetramethyl-2-((2-oxopropyl)thio)imidazolium; 7440-70-2/Calcium; 9001-31-4/Fibrin; 9001-32-5/Fibrinogen; EC 2.3.2.13/Factor XIIIa; EC 3.4.21.5/Thrombin
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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