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超声联合微泡辅助基因转染修复跟腱:长期的基因表达和纤维调节素 KO 表型的恢复。

Ultrasound and microbubble-assisted gene delivery in Achilles tendons: long lasting gene expression and restoration of fibromodulin KO phenotype.

机构信息

Centre de Biophysique Moléculaire UPR 4301 CNRS, Rue Charles Sadron 45071 Orléans Cedex 2, France.

出版信息

J Control Release. 2011 Dec 10;156(2):223-30. doi: 10.1016/j.jconrel.2011.08.020. Epub 2011 Aug 23.

Abstract

The aim of this study is to deliver genes in Achilles tendons using ultrasound and microbubbles. The rationale is to combine ultrasound-assisted delivery and the stimulation of protein expression induced by US. We found that mice tendons injected with 10 μg of plasmid encoding luciferase gene in the presence of 5×10⁵ BR14 microbubbles, exposed to US at 1 MHz, 200 kPa, 40% duty cycle for 10 min were efficiently transfected without toxicity. The rate of luciferase expression was 100-fold higher than that obtained when plasmid alone was injected. Remarkably, the luciferase transgene was stably expressed for up to 108 days. DNA extracted from these sonoporated tendons was efficient in transforming competent E. coli bacteria, indicating that persistent intact pDNA was responsible for this long lasting gene expression. We used this approach to restore expression of the fibromodulin gene in fibromodulin KO mice. A significant fibromodulin expression was detected by quantitative PCR one week post-injection. Interestingly, ultrastructural analysis of these tendons revealed that collagen fibrils diameter distribution and circularity were similar to that of wild type mice. Our results suggest that this gene delivery method is promising for clinical applications aimed at modulating healing or restoring a degenerative tendon while offering great promise for gene therapy due its safety compared to viral methods.

摘要

本研究旨在通过超声和微泡将基因递送至跟腱。其原理是结合超声辅助传递和 US 诱导的蛋白质表达刺激。我们发现,在存在 5×10⁵ BR14 微泡的情况下,向注射了编码荧光素酶基因的 10 μg 质粒的小鼠跟腱中施加 1 MHz、200 kPa、40%占空比的超声 10 min,可有效转染而无毒性。荧光素酶表达率比单独注射质粒时高 100 倍。值得注意的是,荧光素酶转基因可稳定表达长达 108 天。从这些超声处理的肌腱中提取的 DNA 有效地转化了感受态 E. coli 细菌,表明持续完整的 pDNA 是导致这种长期基因表达的原因。我们使用这种方法在纤维调节素 KO 小鼠中恢复纤维调节素基因的表达。注射后一周通过定量 PCR 检测到明显的纤维调节素表达。有趣的是,这些肌腱的超微结构分析显示,胶原纤维直径分布和圆度与野生型小鼠相似。我们的结果表明,这种基因传递方法具有很大的临床应用前景,可用于调节愈合或恢复退行性肌腱,同时由于与病毒方法相比具有更高的安全性,为基因治疗提供了很大的希望。

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