Thrombus Structure
Thrombus Structure - Related Videos
09:01
Intravital Microscopy and Thrombus Induction in the Earlobe of a Hairless Mouse
0 Views •
Cited by 4 •
2017
The ear model of the hairless SKH1-Hrhr mouse enables intravital fluorescence microscopy of microcirculation and phototoxic thrombus induction without prior surgical preparation in the examined microvascular bed. Therefore, the ear of the hairless mouse is an excellent in vivo model to study the complex interactions during microvascular thrombus formation, thrombus evolution, and thrombolysis.
05:54
Intravital Fluorescence Microscopy to Study Microvascular Thrombus Formation
0 Views •
2025
This video demonstrates the intravital fluorescence microscopy technique to study thrombus formation in a mouse model. The mouse is injected with a fluorophore-labeled polysaccharide to monitor blood circulation. Upon illumination with a high-intensity light, the phototoxic induction of an injury in the microvasculature of the ear leads to the formation of a thrombus, which is confirmed by visualizing the obstruction in the blood flow.
02:05
Visualization of a Cerebral Thrombus in a Mouse Using Micro-Computed Tomography Imaging
0 Views •
2025
Source: Kim, D., et. al. Combined Near-infrared Fluorescent Imaging and Micro-computed Tomography for Directly Visualizing Cerebral Thromboemboli. J. Vis. Exp. (2016)This video demonstrates visualization of cerebral thrombus in mice using micro-computed tomography (micro-CT) imaging. A cerebral thrombus mouse model is injected with fibrin-targeted gold nanoparticles acting as a contrasting agent. The mouse is placed on the bed of a micro-CT machine, and images are acquired from multiple angles.
11:18
Real-time Imaging of Heterotypic Platelet-neutrophil Interactions on the Activated Endothelium During Vascular Inflammation and Thrombus Formation in Live Mice
0 Views •
Cited by 29 •
2013
Here we report an experimental technique of fluorescence intravital microscopy to visualize heterotypic platelet-neutrophil interactions on the activated endothelium during vascular inflammation and thrombus formation in live mice. This microscopic technology will be valuable to study the molecular mechanism of vascular disease and to test pharmacologic agents under pathophysiological conditions.
12:03
Dynamics of Structures
0 Views •
2023
Source: Roberto Leon, Department of Civil and Environmental Engineering, Virginia Tech, Blacksburg, VA It is rare nowadays that a whole year goes by without a major earthquake event wreaking havoc somewhere around the world. In some cases, like the 2005 Banda Ache earthquake in Indonesia, the damage involved large geographic areas and casualties in the six figures. In general, the number and intensity of earthquakes is not increasing, however, the vulnerability of the built environment is...
FAQs
Disturbed or stagnant flow changes how blood components interact with the vessel wall and with one another. These conditions support platelet adhesion and activation, followed by coagulation and fibrin formation. The resulting arrangement of platelets, fibrin, red blood cells, and leukocytes can affect whether a thrombus stays attached, enlarges, or obstructs circulation.
Platelets provide an activated cellular framework for clot development, while thrombin links cellular activity to the coagulation process. By converting fibrinogen into fibrin, thrombin produces strands that form a mesh throughout the clot. This network retains blood cells and additional platelets, contributing to the thrombus's organization and mechanical stability.
Arterial and venous thrombosis develop in different flow environments, so their cellular and molecular organization may differ. Disturbed flow promotes platelet adhesion and activation, whereas stagnant conditions also favor coagulation and fibrin deposition. Examining the relative contribution of platelets, fibrin, and trapped blood cells helps distinguish these clinical patterns.
The distribution of fibrin, platelets, red blood cells, and leukocytes provides clues about how a thrombus formed and how stable it may be. A more organized structure can remain attached, whereas changes in cohesion or attachment may influence fragmentation and movement. Structural assessment therefore supports interpretation of possible occlusive or embolic behavior.
Assessment combines information from imaging and pathology findings rather than relying on a single structural feature. Imaging can show the thrombus in relation to the vessel or heart and indicate its effect on circulation, while pathology can reveal its cellular and molecular organization. Together, these approaches help characterize formation, stability, and clinical significance.
Structural findings help clinicians distinguish arterial from venous thrombosis and interpret how a clot relates to impaired blood flow. They can also provide context for whether the thrombus is likely to remain localized, obstruct a vessel, or contribute to embolic risk. This information supports clinical interpretation of imaging and pathological observations.
Anticoagulant and antiplatelet treatments influence different aspects of clot development. Anticoagulant effects relate to coagulation and fibrin generation, whereas antiplatelet effects target platelet participation. Evaluating structural changes after treatment can help researchers determine whether a thrombus forms differently, becomes less stable, or shows altered cellular and molecular organization.
Its organization connects the initiating conditions of thrombosis with clinically relevant outcomes. Studying the arrangement of platelets, fibrin, red blood cells, and leukocytes helps explain differences between arterial and venous disease, supports interpretation of imaging and pathology, and provides a framework for evaluating how therapies modify clot formation, persistence, and potential obstruction.