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

机译:脂质纳米颗粒沉默肿瘤坏死因子α以改善糖尿病小鼠的伤口愈合

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摘要

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.
机译:在美国,糖尿病及其并发症导致的死亡率和发病率越来越受到关注。特别值得关注的是,糖尿病患者经常遭受伤口愈合不良和所导致的糖尿病足溃疡不愈合的困扰。这些溃疡会过度产生肿瘤坏死因子α(TNFα),从而减少伤口床细胞的迁移和增殖,同时促进细胞凋亡。在本文中,我们描述了使用载有siRNA的脂质纳米颗粒(LNP)作为潜在的伤口治疗方法,以对抗过度的免疫反应并促进伤口闭合。 LNP用对TNFα特异性的可电离,可降解的类脂质和siRNA配制。在糖尿病和非糖尿病小鼠中,局部应用纳米颗粒可使伤口中的TNFαmRNA表达降低40-55%。与未治疗的对照组相比,在糖尿病小鼠中,这种TNFα抑制作用可加速伤口愈合。综合起来,这些结果证明了使用LNP进行RNA干扰疗法可以降低慢性糖尿病伤口的严重程度和持续时间的概念证明。

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