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Evolocumab loaded Bio-Liposomes for efficient atherosclerosis therapy
PCSK9, which is closely related to atherosclerosis, is significantly expressed in vascular smooth muscle cells (VSMCs). Moreover, Proprotein Convertase Subtilisin/Kexin type 9 (PCSK9) mediated phenotypic transformation, abnormal proliferation, and migration of VSMCs play key roles in accelerating at...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199622/ https://www.ncbi.nlm.nih.gov/pubmed/37208681 http://dx.doi.org/10.1186/s12951-023-01904-4 |
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author | Li, Zhenxian Zhu, Haimei Liu, Hao Liu, Dayue Liu, Jianhe Jiang, Jiazheng Zhang, Yi Qin, Zhang Xu, Yijia Peng, Yuan Liu, Bin Long, Yun |
author_facet | Li, Zhenxian Zhu, Haimei Liu, Hao Liu, Dayue Liu, Jianhe Jiang, Jiazheng Zhang, Yi Qin, Zhang Xu, Yijia Peng, Yuan Liu, Bin Long, Yun |
author_sort | Li, Zhenxian |
collection | PubMed |
description | PCSK9, which is closely related to atherosclerosis, is significantly expressed in vascular smooth muscle cells (VSMCs). Moreover, Proprotein Convertase Subtilisin/Kexin type 9 (PCSK9) mediated phenotypic transformation, abnormal proliferation, and migration of VSMCs play key roles in accelerating atherosclerosis. In this study, by utilizing the significant advantages of nano-materials, a biomimetic nanoliposome loading with Evolocumab (Evol), a PCSK9 inhibitor, was designed to alleviate atherosclerosis. In vitro results showed that (Lipo + M)@E NPs up-regulated the levels of α-SMA and Vimentin, while inhibiting the expression of OPN, which finally result in the inhibition of the phenotypic transition, excessive proliferation, and migration of VSMCs. In addition, the long circulation, excellent targeting, and accumulation performance of (Lipo + M)@E NPs significantly decreased the expression of PCSK9 in serum and VSMCs within the plaque of ApoE(−/−) mice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-01904-4. |
format | Online Article Text |
id | pubmed-10199622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101996222023-05-21 Evolocumab loaded Bio-Liposomes for efficient atherosclerosis therapy Li, Zhenxian Zhu, Haimei Liu, Hao Liu, Dayue Liu, Jianhe Jiang, Jiazheng Zhang, Yi Qin, Zhang Xu, Yijia Peng, Yuan Liu, Bin Long, Yun J Nanobiotechnology Research PCSK9, which is closely related to atherosclerosis, is significantly expressed in vascular smooth muscle cells (VSMCs). Moreover, Proprotein Convertase Subtilisin/Kexin type 9 (PCSK9) mediated phenotypic transformation, abnormal proliferation, and migration of VSMCs play key roles in accelerating atherosclerosis. In this study, by utilizing the significant advantages of nano-materials, a biomimetic nanoliposome loading with Evolocumab (Evol), a PCSK9 inhibitor, was designed to alleviate atherosclerosis. In vitro results showed that (Lipo + M)@E NPs up-regulated the levels of α-SMA and Vimentin, while inhibiting the expression of OPN, which finally result in the inhibition of the phenotypic transition, excessive proliferation, and migration of VSMCs. In addition, the long circulation, excellent targeting, and accumulation performance of (Lipo + M)@E NPs significantly decreased the expression of PCSK9 in serum and VSMCs within the plaque of ApoE(−/−) mice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-01904-4. BioMed Central 2023-05-19 /pmc/articles/PMC10199622/ /pubmed/37208681 http://dx.doi.org/10.1186/s12951-023-01904-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Li, Zhenxian Zhu, Haimei Liu, Hao Liu, Dayue Liu, Jianhe Jiang, Jiazheng Zhang, Yi Qin, Zhang Xu, Yijia Peng, Yuan Liu, Bin Long, Yun Evolocumab loaded Bio-Liposomes for efficient atherosclerosis therapy |
title | Evolocumab loaded Bio-Liposomes for efficient atherosclerosis therapy |
title_full | Evolocumab loaded Bio-Liposomes for efficient atherosclerosis therapy |
title_fullStr | Evolocumab loaded Bio-Liposomes for efficient atherosclerosis therapy |
title_full_unstemmed | Evolocumab loaded Bio-Liposomes for efficient atherosclerosis therapy |
title_short | Evolocumab loaded Bio-Liposomes for efficient atherosclerosis therapy |
title_sort | evolocumab loaded bio-liposomes for efficient atherosclerosis therapy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199622/ https://www.ncbi.nlm.nih.gov/pubmed/37208681 http://dx.doi.org/10.1186/s12951-023-01904-4 |
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