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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.

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。

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