RIVERSIDE, Calif. (http://www.
While scientists know a lot about how blood clots form, relatively little was known about how they contract -- a slow process that takes an hour to complete.
In an article published recently in Nature Communications, researchers at the University of California, Riverside and the University of Pennsylvania School of Medicine used high-powered microscopy and rheometry--the measurement of how materials become deformed in response to applied force--to view that process in real time and at the cellular level. The findings will be useful in the development of new therapies for clotting disorders.
As a result of injury or inflammation, platelets in blood get activated, become sticky, and bind together and with a stringy protein called fibrin to form a mesh-like plug (the blood clot) that stops bleeding into tissue. Platelets play a central role in clot contraction, but, until now, scientists haven't been able to show exactly how they accomplish this.
As described in the paper, clot shrinkage occurs when platelets form hand-like protrusions called filopodia. These filopodia then attach to fibrin fibers and reel them in using the same hand-over-hand action used by a person pulling on a rope. The platelets retain the fibrin in tiny, tightly wound bundles, therefore remodeling the fibrin mesh to make it more dense and stiff. The reeling action also brings platelets and clusters of platelets closer together, reducing the overall volume of the clot followed by complete dissolution by fibrinolytic enzymes.
The research was led by Mark Alber, a distinguished professor of mathematics in UCR's College of Natural and Agricultural Sciences, and two researchers at the University of Pennsylvania Perelman School of Medicine: John Weisel, professor of cell and developmental biology, and Rustem Litvinov, research scientist. Oleg Kim, a researcher in UC Riverside's College of Natural and Agricultural Sciences and a visiting scientist at the University of Pennsylvania, was the first author on the paper.
Alber said the findings highlight a new role for filopodia, which were previously thought to help cells move around and sense their environment.
"Until now, we knew very little about how individual platelets or small clusters of platelets exert a contractile force on fibrin fibers and how this tension collapses a clot's structure and reduces its size," Alber said. "Through this research, we have revealed a novel function for filopodia, which is their ability to re-arrange the fibrin matrix to cause clot shrinkage. These findings will aid in the design of thrombolytic therapeutics for enhanced treatment of blood disorders, including thrombosis and thromboembolism."
The paper is titled "Quantitative Structural Mechanobiology of Platelet-Driven Blood Clot Contraction." A related paper, "Strong Binding of Platelet Integrin αIIbβ3 to Fibrin Clots: Potential Target to Destabilize Thrombi" recently appeared in Scientific Reports and describes the role of the integrin αIIbβ3 in the formation of obstructive blood clots (thrombi). Contributors are: Peter Höök, University of Notre Dame and first author on the paper; Rustem Litvinov; Oleg Kim; Mark Alber; John Weisel; Shixin Xu, UC Riverside; Zhiliang Xu, University of Pennsylvania; and Joel Bennett, University of Notre Dame.
These newly published results on mechanisms of blood clotting are outcomes of a collaborative project titled "Multiscale modeling and empirical study of a mechanism limiting blood clot growth" between UCR, University of Pennsylvania Perelman School of Medicine, and University of Notre Dame, led by Mark Alber and supported by the National Institutes of Health (NIH) UO1 HL116330 Grant.