Contrast‑enhanced ultrasound molecular imaging of activated platelets in the progression of atherosclerosis using microbubbles bearing the von Willebrand factor A1 domain

Tian,Jie; Weng,Yahui; Sun,Ruiying; Zhu,Ying; Zhang,Jun; Liu,Hongyun; Liu,Yani

doi:10.3892/etm.2021.10153

July-2021 Volume 22 Issue 1

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July-2021 Volume 22 Issue 1

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Article Open Access

Contrast‑enhanced ultrasound molecular imaging of activated platelets in the progression of atherosclerosis using microbubbles bearing the von Willebrand factor A1 domain

Authors:
- Jie Tian
- Yahui Weng
- Ruiying Sun
- Ying Zhu
- Jun Zhang
- Hongyun Liu
- Yani Liu
View Affiliations / Copyright

Affiliations: Department of Medical Ultrasound, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430030, P.R. China

Copyright: © Tian et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Article Number: 721
|
Published online on: May 3, 2021

https://doi.org/10.3892/etm.2021.10153
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Abstract

Platelet‑endothelial interactions have been linked to increased inflammatory activation and a prothrombotic state in atherosclerosis. The interaction between von Willebrand factor (vWF)‑A1 domain and platelet glycoprotein (GP) Ib/IX plays a significant role in mediating the adhesion of platelets to the injured endothelium. In the present study, contrast‑enhanced ultrasound (CEU) molecular imaging with microbubbles bearing the vWF‑A1 domain was performed to non‑invasively monitor activated platelets on the vascular endothelium in the procession of atherosclerosis. A targeted CEU contrast agent was prepared by attaching the vWF‑A1 domain to the shell of microbubbles (Mb_A1). Rat isotype control antibody was used to produce control (Mb_ctrl) microbubbles. The binding of Mb_A1 and Mb_ctrl to activated platelets was assessed in in vitro flow chamber experiments. Apolipoprotein E (ApoE^‑/‑) deficient mice were studied as a model of atherosclerosis. At 8, 16 and 32 weeks of age, CEU molecular imaging of the proximal aorta with Mb_A1 and Mb_ctrl was performed and the imaging signals from microbubbles were quantified. Atherosclerotic lesion severity and platelets on the endothelial surface were assessed by histology and immunohistochemistry. In in vitro flow chamber studies, attachment of MbA1 to activated platelets on culture dishes was significantly greater than that of Mb_ctrl across a range of shear stresses (P<0.05). The attachment of Mbctrl was sparse and not related to the aggregated platelets. As lesion development progressed in the ApoE^‑/‑ mice, molecular imaging of activated platelets demonstrated selective signal enhancement of Mb_A1 (P<0.05 vs. Mb_ctrl) at all ages. Selective signal enhancement from Mb_A1 increased from 8 to 32 weeks of age. Immunohistochemistry for GPIIb revealed the presence of platelets on the endothelial cell surface in each group of ApoE^‑/‑ mice and that the degree of platelet deposits was age‑dependent. The results of the present study indicated that non‑invasive CEU molecular imaging with targeted microbubbles bearing the vWF‑A1 domain could not only detect activated platelets on the vascular endothelium but also indicate lesion severity in atherosclerosis.

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