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Targeted Delivery of Shear Stress-Inducible microRNAs by Nanoparticles to Prevent Vulnerable Atherosclerotic Lesions Cover

Targeted Delivery of Shear Stress-Inducible microRNAs by Nanoparticles to Prevent Vulnerable Atherosclerotic Lesions

Open Access
|Jul 2016

Figures & Tables

Figure 1.

Schematic view of miR-146a and miR-181b microRNAs delivered by E-selectin thioaptamer-multistage vector for treatment of atherosclerosis. CCL2: monocyte chemoattractant protein-1

Figure 2.

Effects of PEG/PEI/micro-RNAs and ESTA-MSV/microRNAs on the aortic atherogenesis of apolipoprotein E-deficient (ApoE−/−) mice. (A) Representative en face Oil Red O-stained aortic arches and thoracic aortae of ApoE−/− mice intravenously injected with vehicle, miR-146a, and miR-181b (15 μg) loaded in PEG/PEI nanoparticles or (C) ESTA-MSV microparticles biweekly for 12 weeks. (B, D) Quantification of en face aortic plaque size. * P < 0.05, **P < 0.01 vs vehicle group. Adapted from Ma et al.51 ESTA-MSV: E-selectin thioaptamer-multistage vector; PEG-PEI: polyethylene glycol-polyethyleneimine

Language: English
Page range: 152 - 156
Published on: Jul 1, 2016
Published by: Houston Methodist DeBakey Heart & Vascular Center
In partnership with: Paradigm Publishing Services

© 2016 Wing Tak Wong, Shuangtao Ma, Xiao Yu Tian, Andrea Banuet Gonzalez, Eno E. Ebong, Haifa Shen, published by Houston Methodist DeBakey Heart & Vascular Center
This work is licensed under the Creative Commons Attribution-NonCommercial 4.0 License.