• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

β-CD-(D) 作为 siRNA 载体降低基质金属蛋白酶-9 表达和改善糖尿病大鼠伤口愈合的效率和安全性。

Efficiency and Safety of β-CD-(D) as siRNA Carrier for Decreasing Matrix Metalloproteinase-9 Expression and Improving Wound Healing in Diabetic Rats.

机构信息

Department of Endocrinology, Sun Yat-sen Memorial Hospital, Guangdong Provincal Key Laboratory of Malignant Tumor Epigenetics and Gene Reguatioǹ Medical Research Center, Sun Yat-sen University , Guangzhou 510120, China.

Department of Endocrinology, The Third Affiliated Hospital of Guangzhou Medical University , Guangzhou 510150, China.

出版信息

ACS Appl Mater Interfaces. 2017 May 24;9(20):17417-17426. doi: 10.1021/acsami.7b02809. Epub 2017 May 5.

DOI:10.1021/acsami.7b02809
PMID:28447455
Abstract

Overexpression of matrix metalloproteinase-9 (MMP-9) is critical for diabetic chronic wounds involved in the refractory wound healing process. We aimed to develop a strategy through RNAi to decrease MMP-9 expression and improve diabetic wound healing. We had explored β-CD-(D) as a gene carrier to take siRNA and effectively interfere with MMP-9 expression. It has been proven that β-CD-(D) could be used as an effective siRNA delivery system. In this study, we want to know about the efficiency and safety of β-CD-(D)/MMP-9 siRNA for improving wound healing in diabetic rats. β-CD-(D3)7/MMP-9 siRNA treated animals show lower levels of MMP-9 expression, which induce faster wound-close rates. Histological evaluation indicates that β-CD-(D3)7/MMP-9 siRNA significantly increases the content of collagen around the injured tissues. The number of neutrophilic ganulocytes was significantly decreased through treatment of β-CD-(D3)7/MMP-9 siRNA. In vivo fluorescence imaging assessment shows that β-CD-(D3)7/MMP-9 siRNA could not cause organ damage and organ accumulation. The results suggest that β-CD-(D)/MMP-9 siRNA might be developed as a novel topical agent for the diabetic wounds treatment.

摘要

基质金属蛋白酶-9(MMP-9)的过表达对于涉及难治性伤口愈合过程的糖尿病慢性伤口至关重要。我们旨在通过 RNAi 开发一种策略来降低 MMP-9 的表达并改善糖尿病伤口愈合。我们已经探索了β-CD-(D)作为一种基因载体来携带 siRNA 并有效干扰 MMP-9 的表达。已经证明β-CD-(D)可以用作有效的 siRNA 递送系统。在这项研究中,我们想了解β-CD-(D3)7/MMP-9 siRNA 改善糖尿病大鼠伤口愈合的效率和安全性。β-CD-(D3)7/MMP-9 siRNA 处理的动物表现出较低水平的 MMP-9 表达,从而诱导更快的伤口闭合率。组织学评估表明,β-CD-(D3)7/MMP-9 siRNA 显著增加了受伤组织周围胶原蛋白的含量。通过β-CD-(D3)7/MMP-9 siRNA 处理,中性粒细胞的数量明显减少。体内荧光成像评估表明,β-CD-(D3)7/MMP-9 siRNA 不会引起器官损伤和器官积累。结果表明,β-CD-(D)/MMP-9 siRNA 可能被开发为治疗糖尿病伤口的新型局部制剂。

相似文献

1
Efficiency and Safety of β-CD-(D) as siRNA Carrier for Decreasing Matrix Metalloproteinase-9 Expression and Improving Wound Healing in Diabetic Rats.β-CD-(D) 作为 siRNA 载体降低基质金属蛋白酶-9 表达和改善糖尿病大鼠伤口愈合的效率和安全性。
ACS Appl Mater Interfaces. 2017 May 24;9(20):17417-17426. doi: 10.1021/acsami.7b02809. Epub 2017 May 5.
2
Cationic star-shaped polymer as an siRNA carrier for reducing MMP-9 expression in skin fibroblast cells and promoting wound healing in diabetic rats.阳离子星形聚合物作为 siRNA 载体,降低皮肤成纤维细胞中 MMP-9 的表达,促进糖尿病大鼠伤口愈合。
Int J Nanomedicine. 2014 Jul 15;9:3377-87. doi: 10.2147/IJN.S66368. eCollection 2014.
3
45S5 Bioglass® works synergistically with siRNA to downregulate the expression of matrix metalloproteinase-9 in diabetic wounds.45S5 生物玻璃®与 siRNA 协同作用,下调糖尿病创面基质金属蛋白酶-9 的表达。
Acta Biomater. 2022 Jun;145:372-389. doi: 10.1016/j.actbio.2022.04.010. Epub 2022 Apr 12.
4
Naturally-occurring bacterial cellulose-hyperbranched cationic polysaccharide derivative/MMP-9 siRNA composite dressing for wound healing enhancement in diabetic rats.用于增强糖尿病大鼠伤口愈合的天然细菌纤维素-超支化阳离子多糖衍生物/MMP-9 siRNA 复合敷料。
Acta Biomater. 2020 Jan 15;102:298-314. doi: 10.1016/j.actbio.2019.11.005. Epub 2019 Nov 18.
5
Mesenchymal stem cells correct impaired diabetic wound healing by decreasing ECM proteolysis.间充质干细胞通过减少细胞外基质蛋白水解来纠正受损的糖尿病创面愈合。
Physiol Genomics. 2017 Oct 1;49(10):541-548. doi: 10.1152/physiolgenomics.00090.2016. Epub 2017 Aug 25.
6
Sustained delivery of MMP-9 siRNA via thermosensitive hydrogel accelerates diabetic wound healing.温敏水凝胶持续递送 MMP-9 siRNA 加速糖尿病创面愈合。
J Nanobiotechnology. 2021 May 5;19(1):130. doi: 10.1186/s12951-021-00869-6.
7
Efficiency and Safety of Dextran-PAMAM/siMMP-9 Complexes for Decreasing Matrix Metalloproteinase-9 Expression and Promoting Wound Healing in Diabetic Rats.聚酰胺-胺树枝状聚合物/小分子干扰 RNA 复合物降低基质金属蛋白酶-9 表达促进糖尿病大鼠创面愈合的效率和安全性。
Bioconjug Chem. 2022 Dec 21;33(12):2398-2410. doi: 10.1021/acs.bioconjchem.2c00487. Epub 2022 Nov 14.
8
Hyperbranched cationic polysaccharide derivatives for efficient siRNA delivery and diabetic wound healing enhancement.超支化阳离子多糖衍生物用于高效 siRNA 递送和糖尿病伤口愈合的增强。
Int J Biol Macromol. 2020 Jul 1;154:855-865. doi: 10.1016/j.ijbiomac.2020.03.164. Epub 2020 Mar 18.
9
Matrix metalloproteinase-inspired suicidal treatments of diabetic ulcers with siRNA-decorated nanofibrous meshes.基于基质金属蛋白酶的仿生自杀治疗法,用 siRNA 修饰的纳米纤维网治疗糖尿病溃疡。
Gene Ther. 2013 Apr;20(4):378-85. doi: 10.1038/gt.2012.49. Epub 2012 Jun 21.
10
Self-Assembled Wound Dressings Silence MMP-9 and Improve Diabetic Wound Healing In Vivo.自组装伤口敷料可抑制基质金属蛋白酶-9并促进糖尿病伤口的体内愈合。
Adv Mater. 2016 Mar 2;28(9):1809-17. doi: 10.1002/adma.201503565. Epub 2015 Dec 23.

引用本文的文献

1
Extracellular Vesicle-Associated miR-ERIA Exerts the Antiangiogenic Effect of Macrophages in Diabetic Wound Healing.细胞外囊泡相关的miR-ERIA在糖尿病伤口愈合中发挥巨噬细胞的抗血管生成作用。
Diabetes. 2025 Apr 1;74(4):596-610. doi: 10.2337/db24-0701.
2
Advances in nucleic acid delivery strategies for diabetic wound therapy.用于糖尿病伤口治疗的核酸递送策略的进展。
J Clin Transl Endocrinol. 2024 Aug 30;37:100366. doi: 10.1016/j.jcte.2024.100366. eCollection 2024 Sep.
3
Cas13b-mediated RNA targeted therapy alleviates genetic dilated cardiomyopathy in mice.
Cas13b介导的RNA靶向治疗可减轻小鼠的遗传性扩张型心肌病。
Cell Biosci. 2024 Jan 4;14(1):4. doi: 10.1186/s13578-023-01143-y.
4
In-silico engineering of RNA nanoplatforms to promote the diabetic wound healing.用于促进糖尿病伤口愈合的RNA纳米平台的计算机辅助工程设计。
BMC Chem. 2023 Jun 8;17(1):52. doi: 10.1186/s13065-023-00969-4.
5
Recent advances in responsive hydrogels for diabetic wound healing.用于糖尿病伤口愈合的响应性水凝胶的最新进展。
Mater Today Bio. 2022 Dec 1;18:100508. doi: 10.1016/j.mtbio.2022.100508. eCollection 2023 Feb.
6
Role of matrix metalloproteinases in diabetic foot ulcers: Potential therapeutic targets.基质金属蛋白酶在糖尿病足溃疡中的作用:潜在的治疗靶点。
Front Pharmacol. 2022 Oct 20;13:1050630. doi: 10.3389/fphar.2022.1050630. eCollection 2022.
7
Immunomodulatory biomaterial-based wound dressings advance the healing of chronic wounds via regulating macrophage behavior.基于免疫调节生物材料的伤口敷料通过调节巨噬细胞行为促进慢性伤口愈合。
Regen Biomater. 2022 Sep 6;9:rbac065. doi: 10.1093/rb/rbac065. eCollection 2022.
8
ADSC-exo@MMP-PEG smart hydrogel promotes diabetic wound healing by optimizing cellular functions and relieving oxidative stress.负载脂肪间充质干细胞外泌体的基质金属蛋白酶-聚乙二醇智能水凝胶通过优化细胞功能和减轻氧化应激促进糖尿病伤口愈合。
Mater Today Bio. 2022 Jul 16;16:100365. doi: 10.1016/j.mtbio.2022.100365. eCollection 2022 Dec.
9
Macrophages as a therapeutic target to promote diabetic wound healing.巨噬细胞作为治疗靶点促进糖尿病创面愈合。
Mol Ther. 2022 Sep 7;30(9):2891-2908. doi: 10.1016/j.ymthe.2022.07.016. Epub 2022 Aug 2.
10
The Emerging Role of Immune Cells and Targeted Therapeutic Strategies in Diabetic Wounds Healing.免疫细胞与靶向治疗策略在糖尿病伤口愈合中的新作用
J Inflamm Res. 2022 Jul 20;15:4119-4138. doi: 10.2147/JIR.S371939. eCollection 2022.