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Fibrillin containing elastic microfibrils support platelet adhesion under dynamic shear conditions
J M Ross1, L V McIntire, J L Moake
1Cox Laboratory for Biomedical Engineering, Rice University, Houston, TX, USA. jross@umbc.edu
Thrombosis and Haemostasis
|February 12, 1998
Summary
Elastic microfibrils promote platelet adhesion and aggregation, mediated by the GPIIb-IIIa receptor, under low shear conditions. They do not support mural thrombus formation under high shear, suggesting roles in vascular injury responses.
Area of Science:
- Biochemistry
- Vascular Biology
- Platelet Physiology
Background:
- The vascular subendothelium contains microfibrils, including Type VI collagen, crucial for platelet adhesion and aggregation.
- Previous research explored platelet receptors and von Willebrand factor (vWf) in these processes under physiological shear.
Purpose of the Study:
- To investigate the role of fibrillin-containing elastic microfibrils in supporting mural thrombus formation.
- To elucidate the mechanisms of platelet interaction with elastic microfibrils under varying shear conditions.
Main Methods:
- Assessing platelet adhesion and aggregation on elastic microfibril surfaces.
- Evaluating the involvement of the GPIIb-IIIa platelet receptor.
- Testing thrombus formation under low and high shear conditions.
Main Results:
- Elastic microfibrils supported platelet adhesion similarly to collagen VI tetramers under low shear.
- Significantly higher platelet aggregation occurred on elastic microfibrils compared to collagen VI.
- Platelet adhesion and aggregation on elastic microfibrils were mediated by the GPIIb-IIIa receptor.
- Elastic microfibrils did not support mural thrombus formation under high shear conditions.
Conclusions:
- Fibrillin-containing elastic microfibrils play a role in platelet adhesion and aggregation, particularly under low shear stress.
- Both collagen VI and elastic microfibrils contribute to modulating platelet responses following blood vessel injury.
- The GPIIb-IIIa receptor is a key mediator of platelet interaction with elastic microfibrils.
Keywords:
Non-programmatic