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脂质纳米颗粒可沉默肿瘤坏死因子α以促进糖尿病小鼠伤口愈合。

Lipid nanoparticles silence tumor necrosis factor α to improve wound healing in diabetic mice.

作者信息

Kasiewicz Lisa N, Whitehead Kathryn A

机构信息

Dept. of Chemical Engineering Carnegie Mellon University 5000 Forbes Avenue, Pittsburgh PA 15213.

Dept. of Biomedical Engineering Carnegie Mellon University 5000 Forbes Avenue, Pittsburgh PA 15213.

出版信息

Bioeng Transl Med. 2018 Dec 20;4(1):75-82. doi: 10.1002/btm2.10123. eCollection 2019 Jan.

Abstract

Diabetes mellitus is a mounting concern in the United States, as are the mortality and morbidity that result from its complications. Of particular concern, diabetes patients frequently suffer from impaired wound healing and resultant nonhealing diabetic foot ulcers. These ulcers overproduce tumor necrosis factor α (TNFα), which reduces wound bed cell migration and proliferation while encouraging apoptosis. Herein, we describe the use of siRNA-loaded lipid nanoparticles (LNPs) as a potential wound treatment to combat an overzealous immune response and facilitate wound closure. LNPs were formulated with an ionizable, degradable lipidoid and siRNA specific for TNFα. Topical application of nanoparticles reduced TNFα mRNA expression in the wound by 40-55% in diabetic and nondiabetic mice. In diabetic mice, this TNFα knockdown accelerated wound healing compared to untreated controls. Together, these results serve as proof-of-concept that RNA interference therapy using LNPs can reduce the severity and duration of chronic diabetic wounds.

摘要

糖尿病在美国正日益引起关注,其并发症导致的死亡率和发病率亦是如此。特别值得关注的是,糖尿病患者经常遭受伤口愈合受损以及由此产生的不愈合糖尿病足溃疡。这些溃疡会过度产生肿瘤坏死因子α(TNFα),这会减少伤口床细胞的迁移和增殖,同时促进细胞凋亡。在此,我们描述了负载小干扰RNA(siRNA)的脂质纳米颗粒(LNP)作为一种潜在的伤口治疗方法,以对抗过度活跃的免疫反应并促进伤口愈合。LNP是用一种可电离、可降解的类脂质和针对TNFα的siRNA配制而成。纳米颗粒的局部应用使糖尿病和非糖尿病小鼠伤口中的TNFα信使核糖核酸(mRNA)表达降低了40%至55%。在糖尿病小鼠中,与未治疗的对照组相比,这种TNFα基因敲低加速了伤口愈合。总之,这些结果证明了使用LNP的RNA干扰疗法可以减轻慢性糖尿病伤口的严重程度并缩短其持续时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03bd/6336737/cc887c059a40/BTM2-4-75-g001.jpg

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