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Ultrasound-Aided Targeting Nanoparticles Loaded with miR-181b for Anti-Inflammatory Treatment of TNF-α-Stimulated Endothelial Cells
[Image: see text] Gene therapy is an emerging therapeutic strategy used in clinics. Ultrasound-mediated gene transfection possesses great potential as a secure and available approach for gene delivery. However, transfection efficiency and targeting ability remain challenging. In this study, we devel...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376683/ https://www.ncbi.nlm.nih.gov/pubmed/32715195 http://dx.doi.org/10.1021/acsomega.0c00823 |
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author | Liu, Donghong Liu, Jia Li, Chao Li, Wei Wang, Wei Liu, Jie |
author_facet | Liu, Donghong Liu, Jia Li, Chao Li, Wei Wang, Wei Liu, Jie |
author_sort | Liu, Donghong |
collection | PubMed |
description | [Image: see text] Gene therapy is an emerging therapeutic strategy used in clinics. Ultrasound-mediated gene transfection possesses great potential as a secure and available approach for gene delivery. However, transfection efficiency and targeting ability remain challenging. In this study, we developed a kind of ultrasound-aided and targeting nanoparticles for microRNA delivery. These nanoparticles carrying nucleic acids were prepared with cationic poly-(amino acid) encapsulated with perfluoropentane. The formulated nanoparticles were stabilized with negatively charged PGA–PEG–RGD peptide coating. Ultrasound imaging and specific gene transfection using this nanocarrier could be implemented simultaneously. Upon treatment with ultrasound irradiation, phase transition was induced in the nanoparticles and they generated acoustic cavitation, resulting in enhanced gene transfection against the endothelial cells. With the overexpression of miR-181b loaded by the nanoparticles, the TNF-α-stimulated endothelial cells were effectively rescued from the inflammatory state through the protection of cell viability and suppression of cell adhesion. |
format | Online Article Text |
id | pubmed-7376683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73766832020-07-24 Ultrasound-Aided Targeting Nanoparticles Loaded with miR-181b for Anti-Inflammatory Treatment of TNF-α-Stimulated Endothelial Cells Liu, Donghong Liu, Jia Li, Chao Li, Wei Wang, Wei Liu, Jie ACS Omega [Image: see text] Gene therapy is an emerging therapeutic strategy used in clinics. Ultrasound-mediated gene transfection possesses great potential as a secure and available approach for gene delivery. However, transfection efficiency and targeting ability remain challenging. In this study, we developed a kind of ultrasound-aided and targeting nanoparticles for microRNA delivery. These nanoparticles carrying nucleic acids were prepared with cationic poly-(amino acid) encapsulated with perfluoropentane. The formulated nanoparticles were stabilized with negatively charged PGA–PEG–RGD peptide coating. Ultrasound imaging and specific gene transfection using this nanocarrier could be implemented simultaneously. Upon treatment with ultrasound irradiation, phase transition was induced in the nanoparticles and they generated acoustic cavitation, resulting in enhanced gene transfection against the endothelial cells. With the overexpression of miR-181b loaded by the nanoparticles, the TNF-α-stimulated endothelial cells were effectively rescued from the inflammatory state through the protection of cell viability and suppression of cell adhesion. American Chemical Society 2020-07-07 /pmc/articles/PMC7376683/ /pubmed/32715195 http://dx.doi.org/10.1021/acsomega.0c00823 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Liu, Donghong Liu, Jia Li, Chao Li, Wei Wang, Wei Liu, Jie Ultrasound-Aided Targeting Nanoparticles Loaded with miR-181b for Anti-Inflammatory Treatment of TNF-α-Stimulated Endothelial Cells |
title | Ultrasound-Aided Targeting Nanoparticles Loaded with
miR-181b for Anti-Inflammatory Treatment of TNF-α-Stimulated
Endothelial Cells |
title_full | Ultrasound-Aided Targeting Nanoparticles Loaded with
miR-181b for Anti-Inflammatory Treatment of TNF-α-Stimulated
Endothelial Cells |
title_fullStr | Ultrasound-Aided Targeting Nanoparticles Loaded with
miR-181b for Anti-Inflammatory Treatment of TNF-α-Stimulated
Endothelial Cells |
title_full_unstemmed | Ultrasound-Aided Targeting Nanoparticles Loaded with
miR-181b for Anti-Inflammatory Treatment of TNF-α-Stimulated
Endothelial Cells |
title_short | Ultrasound-Aided Targeting Nanoparticles Loaded with
miR-181b for Anti-Inflammatory Treatment of TNF-α-Stimulated
Endothelial Cells |
title_sort | ultrasound-aided targeting nanoparticles loaded with
mir-181b for anti-inflammatory treatment of tnf-α-stimulated
endothelial cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376683/ https://www.ncbi.nlm.nih.gov/pubmed/32715195 http://dx.doi.org/10.1021/acsomega.0c00823 |
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