Literature DB >> 27119438

Molecular Ultrasound Imaging of αvβ3-Integrin Expression in Carotid Arteries of Pigs After Vessel Injury.

Anne Rix1, Stanley Fokong, Sarah Heringer, Rastislav Pjontek, Lisa Kabelitz, Benjamin Theek, Marc-Alexander Brockmann, Martin Wiesmann, Fabian Kiessling.   

Abstract

OBJECTIVES: Interventions such as balloon angioplasty can cause vascular injury leading to platelet activation, thrombus formation, and inflammatory response. This induces vascular smooth muscle cell activation and subsequent re-endothelialization with expression of αvβ3-integrin by endothelial cells and vascular smooth muscle cell. Thus, poly-N-butylcyanoacrylate microbubbles (MBs) targeted to αvβ3-integrin were evaluated for monitoring vascular healing after vessel injury in pigs using molecular ultrasound imaging.
MATERIALS AND METHODS: Approval for animal experiments was obtained. The binding specificity of αvβ3-integrin-targeted MB to human umbilical vein endothelial cells was tested with fluorescence microscopy. In vivo imaging was performed using a clinical ultrasound system and an 8-MHz probe. Six mini pigs were examined after vessel injury in the left carotid artery. The right carotid served as control. Uncoated MB, cDRG-coated MB, and αvβ3-integrin-specific cRGD-coated MB were injected sequentially. Bound MBs were assessed 8 minutes after injection using ultrasound replenishment analysis. Measurements were performed 2 hours, 1 and 5 weeks, and 3 and 6 months after injury. In vivo data were validated by immunohistochemistry.
RESULTS: Significantly stronger binding of cRGD-MB than MB and cDRG-MB to human umbilical vein endothelial cells was found (P < 0.01). As vessel injury leads to upregulation of αvβ3-integrin, cRGD-MBs bound significantly stronger (P < 0.05) in injured carotid arteries than at the counter side 1 week after vessel injury and significant differences could also be observed after 5 weeks. After 3 months, αvβ3-integrin expression decreased to baseline and binding of cRGD-MB was comparable in both vessels. Values remained at baseline also after 6 months.
CONCLUSIONS: Ultrasound imaging with RGD-MB is promising for monitoring vascular healing after vessel injury. This may open new perspectives to assess vascular damage after radiological interventions.

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Year:  2016        PMID: 27119438     DOI: 10.1097/RLI.0000000000000282

Source DB:  PubMed          Journal:  Invest Radiol        ISSN: 0020-9996            Impact factor:   6.016


  6 in total

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Journal:  Mol Imaging Biol       Date:  2018-12       Impact factor: 3.488

2.  PBCA-based polymeric microbubbles for molecular imaging and drug delivery.

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3.  Fe3O4-based PLGA nanoparticles as MR contrast agents for the detection of thrombosis.

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4.  Molecular ultrasound imaging of JAM-A depicts early arterial inflammation.

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5.  Targeting and Modulation of Liver Myeloid Immune Cells by Hard-Shell Microbubbles.

Authors:  Klaudia T Warzecha; Matthias Bartneck; Diana Möckel; Lia Appold; Can Ergen; Wáel Al Rawashdeh; Felix Gremse; Patricia M Niemietz; Willi Jahnen-Dechent; Christian Trautwein; Fabian Kiessling; Twan Lammers; Frank Tacke
Journal:  Adv Biosyst       Date:  2018-05

6.  Monitoring the Remodeling of Biohybrid Tissue-Engineered Vascular Grafts by Multimodal Molecular Imaging.

Authors:  Elena Rama; Saurav Ranjan Mohapatra; Christoph Melcher; Teresa Nolte; Seyed Mohammadali Dadfar; Ramona Brueck; Vertika Pathak; Anne Rix; Thomas Gries; Volkmar Schulz; Twan Lammers; Christian Apel; Stefan Jockenhoevel; Fabian Kiessling
Journal:  Adv Sci (Weinh)       Date:  2022-02-04       Impact factor: 16.806

  6 in total

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