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一种用于通过小干扰RNA实现高效局部基因沉默的去端肽胶原蛋白涂层

An Atelocollagen Coating for Efficient Local Gene Silencing by Using Small Interfering RNA.

作者信息

Koenig Olivia, Nothdurft Dimitrios, Perle Nadja, Neumann Bernd, Behring Andreas, Degenkolbe Ilka, Walker Tobias, Schlensak Christian, Wendel Hans Peter, Nolte Andrea

机构信息

Department of Thoracic, Cardiac, and Vascular Surgery, University Hospital Tuebingen, Tuebingen, 72076 Baden-Wuerttemberg, Germany.

Department of Thoracic, Cardiac, and Vascular Surgery, University Hospital Tuebingen, Tuebingen, 72076 Baden-Wuerttemberg, Germany.

出版信息

Mol Ther Nucleic Acids. 2017 Mar 17;6:290-301. doi: 10.1016/j.omtn.2017.01.006. Epub 2017 Feb 9.

DOI:10.1016/j.omtn.2017.01.006
PMID:28325296
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5363512/
Abstract

In the last decades, many efforts have been made to counteract adverse effects after stenting atherosclerotic coronary arteries. A breakthrough in better vascular wall regeneration was noted in the new era of drug-eluting stents. A novel personalized approach is the development of gene-eluting stents promising an alteration in gene expression involved in regeneration. We investigated a coating system consisting of the polymer atelocollagen (ATCOL) and a specific small interfering RNA (siRNA) for intercellular adhesion molecule-1 (ICAM-1) found on the surface of defective endothelial cells (ECs). We demonstrated very high cell viability, in which EA.hy926 grew on 0.008% or 0.032% ATCOL layers. Additionally, hemocompatibility assays proved the biocompatibility of this coating. The highest transfection efficiency with EA.hy926 was achieved with 5 μg siRNA immobilized in ATCOL after 2 days. The release of fluorescent-labeled siRNA was about 9 days. Long-term knockdown of ICAM-1 was analyzed by flow cytometry, revealing that the coating with 0.008% ATCOL and 5 μg siICAM-1 provoked gene silencing up to 8 days. 5'-RNA ligase-mediated rapid amplification of cDNA ends PCR (RLM-RACE-PCR) demonstrated the specificity of our established ATCOL gene-silencing coating, meaning that our coating is well suited for further investigations in in vivo studies. Herein, we would like to demonstrate that our ATCOL is well-suited for better artery wall regeneration after stent implantation.

摘要

在过去几十年中,人们为对抗冠状动脉粥样硬化支架置入后的不良反应付出了诸多努力。药物洗脱支架的新时代见证了血管壁再生方面的一项突破。一种新颖的个性化方法是开发基因洗脱支架,有望改变参与再生过程的基因表达。我们研究了一种由去端胶原蛋白(ATCOL)聚合物和一种针对缺陷内皮细胞(ECs)表面发现的细胞间黏附分子-1(ICAM-1)的特异性小干扰RNA(siRNA)组成的涂层系统。我们证明了细胞活力非常高,EA.hy926细胞能在0.008%或0.032%的ATCOL层上生长。此外,血液相容性检测证明了这种涂层的生物相容性。2天后,固定在ATCOL中的5μg siRNA对EA.hy926实现了最高转染效率。荧光标记的siRNA释放约持续9天。通过流式细胞术分析ICAM-1的长期敲低情况,发现含有0.008% ATCOL和5μg siICAM-1的涂层可引发长达8天的基因沉默。5'-RNA连接酶介导的cDNA末端快速扩增PCR(RLM-RACE-PCR)证明了我们所建立的ATCOL基因沉默涂层的特异性,这意味着我们的涂层非常适合在体内研究中进行进一步研究。在此,我们想要证明我们的ATCOL非常适合支架植入后更好地实现动脉壁再生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/58264f3fa945/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/3d48e63f1aa4/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/d597c908bd09/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/3f1db0e7c37e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/e4a3bb808b97/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/992e0cb8d8fa/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/09c17627ccd4/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/e43540f58c4c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/58264f3fa945/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/3d48e63f1aa4/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/d597c908bd09/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/3f1db0e7c37e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/e4a3bb808b97/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/992e0cb8d8fa/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/09c17627ccd4/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/e43540f58c4c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3463/5363512/58264f3fa945/gr7.jpg

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