4.7 Article

CC Chemokine Receptor 5 Targeted Nanoparticles Imaging the Progression and Regression of Atherosclerosis Using Positron Emission Tomography/Computed Tomography

Journal

MOLECULAR PHARMACEUTICS
Volume 18, Issue 3, Pages 1386-1396

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.0c01183

Keywords

nanoparticle; CCR5; atherosclerosis; positron emission tomography; macrophage

Funding

  1. National Heart, Lung, and Blood Institute of the National Institutes of Health [1R35HL145212, R01HL138163]
  2. [DMR1720256]

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Chemokine receptor 5 (CCR5) plays a crucial role in the development of atherosclerosis, with CCR5 antagonists showing potential for inhibiting disease progression. Targeted nanoparticles for CCR5 can sensitively detect atherosclerotic lesions, making them promising for atherosclerosis imaging applications.
Chemokines and chemokine receptors play an important role in the initiation and progression of atherosclerosis by mediating the trafficking of inflammatory cells. Chemokine receptor 5 (CCR5) has major implications in promoting the development of plaques to advanced stage and related vulnerability. CCR5 antagonist has demonstrated the effective inhibition of atherosclerotic progression in mice, making it a potential biomarker for atherosclerosis management. To accurately determine CCR5 in vivo, we synthesized CCR5 targeted Comb nanoparticles through a modular design and construction strategy with control over the physiochemical properties and functionalization of CCR5 targeting peptide D-Ala-peptide T-amide (DAPTAComb). In vivo pharmacokinetic evaluation through Cu-64 radiolabeling showed extended blood circulation of Cu-64-DAPTA-Combs conjugated with 10%, 25%, and 40% DAPTA. The different organ distribution profiles of the three nanoparticles demonstrated the effect of DAPTA on not only physicochemical properties but also targeting efficiency. In vivo positron emission tomography/computed tomography (PET/CT) imaging in an apolipoprotein E knockout mouse atherosclerosis model (ApoE(-/-)) showed that the three Cu-64-DAPTA-Combs could sensitively and specifically detect CCR5 along the progression of atherosclerotic lesions. In an ApoE-encoding adenoviral vector (AAV) induced plaque regression ApoE(-/-) mouse model, decreased monocyte recruitment, CD68(+) macrophages, CCR5 expression, and plaque size were all associated with reduced PET signals, which not only further confirmed the targeting efficiency of Cu-64-DAPTA-Combs but also highlighted the potential of these targeted nanoparticles for atherosclerosis imaging. Moreover, the up-regulation of CCR5 and colocalization with CD68(+) macrophages in the necrotic core of ex vivo human plaque specimens warrant further investigation for atherosclerosis prognosis.

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