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首页> 外文期刊>Ultrasound in Medicine and Biology >SHORT HAIRPIN RNA KNOCKDOWN OF CONNECTIVE TISSUE GROWTH FACTOR BY ULTRASOUND-TARGETED MICROBUBBLE DESTRUCTION IMPROVES RENAL FIBROSIS
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SHORT HAIRPIN RNA KNOCKDOWN OF CONNECTIVE TISSUE GROWTH FACTOR BY ULTRASOUND-TARGETED MICROBUBBLE DESTRUCTION IMPROVES RENAL FIBROSIS

机译:超声靶向微泡破坏法对结缔组织生长因子的短发RNA抑制作用,促进肾纤维化

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The purpose of this study was to evaluate whether ultrasound-targeted microbubble destruction transfer of interfering RNA against connective tissue growth factor (CTGF) in the kidney would ameliorate renal fibrosis in vivo. A short hairpin RNA (shRNA) targeting CTGF was cloned into a tool plasmid and loaded onto the surface of a cationic microbubble product. A unilateral ureteral obstruction (UUO) model in mice was used to evaluate the effect of CTGF knockdown. Mice were administered the plasmid-carrying microbubble intravenously, and ultrasound was applied locally to the obstructed kidney. Mice undergoing a sham UUO surgery and untreated UUO mice were used as disease controls, and mice administered plasmid alone, plasmid with ultrasound treatment and microbubbles and plasmid without ultrasound were used as treatment controls. Mice were treated once and then evaluated at day 14. CTGF in the kidney was measured by quantitative reverse transcription polymerase chain reaction and Western blot. Expression of CTGF, transforming growth factor beta 1, alpha smooth muscle actin and type I collagen in the obstructed kidney was evaluated by immunohistochemistry. The cohort treated with plasmid-carrying microbubbles and ultrasound exhibited reduced mRNA and protein expression of CTGF (p < 0.01). Furthermore, CTGF gene silencing decreased the interstitial deposition of transforming growth factor beta 1, alpha smooth muscle actin and type I collagen as assessed in immunohistochemistry, as well as reduced renal fibrosis in pathologic alterations (p < 0.01). No significant changes in target mRNA, protein expression or disease pathology were observed in the control cohorts. A single treatment of ultrasound-targeted microbubble destruction is able to deliver sufficient shRNA to inhibit the expression of CTGF and provide a meaningful reduction in disease severity. This technique may be a potential therapy for treatment of renal fibrosis. (E-mail: yb12yx@hotmail.com) (C) 2016 World Federation for Ultrasound in Medicine & Biology.
机译:这项研究的目的是评估肾脏中针对靶向结缔组织生长因子(CTGF)的干扰RNA的超声靶向微泡破坏转移是否会改善体内的肾纤维化。将靶向CTGF的短发夹RNA(shRNA)克隆到工具质粒中,并加载到阳离子微泡产物的表面。使用小鼠单侧输尿管梗阻(UUO)模型评估CTGF敲低的效果。静脉内给予小鼠携带质粒的微泡,并在阻塞的肾脏局部施加超声。将接受假UUO手术的小鼠和未治疗的UUO小鼠用作疾病对照,并将仅给予质粒,经超声处理的质粒和微泡以及无超声的质粒的小鼠用作治疗对照。处理小鼠一次,然后在第14天进行评估。通过定量逆转录聚合酶链反应和蛋白质印迹来测量肾脏中的CTGF。通过免疫组织化学评估CTGF,转化生长因子β1,α平滑肌肌动蛋白和I型胶原在阻塞性肾脏中的表达。用携带质粒的微泡和超声处理的队列显示CTGF的mRNA和蛋白表达降低(p <0.01)。此外,CTGF基因沉默可减少转化生长因子β1,α平滑肌肌动蛋白和I型胶原的间质沉积(如免疫组织化学所评估),并减少病理改变中的肾纤维化(p <0.01)。在对照队列中未观察到靶mRNA,蛋白质表达或疾病病理的显着变化。超声靶向微泡破坏的单一治疗能够递送足够的shRNA来抑制CTGF的表达,并显着降低疾病的严重程度。该技术可能是治疗肾纤维化的潜在疗法。 (电子邮件:yb12yx@hotmail.com)(C)2016世界医学和生物学超声联合会。

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