Liang Weihua, Zhang Weiwei, Zhao Shifu, Li Qianning, Yang Yiming, Liang Hua, Ceng Rongchuan
Department of Neurology, Xinqiao Hospital, The Third Military Medical University, Chongqing 400038, P.R. China.
Deparment of Neurology, General Hospital of Beijing PLA Military Region, Beijing 100700, P.R. China.
Mol Med Rep. 2015 Feb;11(2):903-9. doi: 10.3892/mmr.2014.2822. Epub 2014 Oct 30.
The efficiency of cellular uptake of triplex‑forming oligodexinucleotides (TFO), and the inhibition of tissue factor (TF) is low. The aim of the present study was to improve the absorption of TFO, and increase the inhibition of TF induced by shear stress both in vitro and in vivo, by using an ultrasound‑targeted microbubble destruction (UTMD)‑based delivery system. TFO‑conjugated lipid ultrasonic microbubbles (TFO‑M) were first constructed and characterised. The absorption of TFO was observed by a fluorescence‑based method, and the inhibition of TF by immunofluorescence and quantitative polymerase chain reaction. ECV304 human umbilical vein endothelial cells were subjected to fluid shear stress for 6 h after treatment with TFO conjugated lipid ultrasonic microbubbles without sonication (TFO‑M group); TFO alone; TFO conjugated lipid ultrasonic microbubbles, plus immediate sonication (TFO+U group and TFO‑M+U group); or mock treated with 0.9% NaCl only (SSRE group). The in vivo experiments were established in a similar manner to the in vitro experiments, except that TFO or TFO‑M was injected into rats through the tail vein. Six hours after the preparation of a carotid stenosis model, the rats were humanely sacrificed. The transfection efficiency of TFO in the TFO‑M+U group was higher as compared with the TFO‑M and TFO+U group (P<0.01). The protein and mRNA expression of TF in the TFO‑M+U group was significantly decreased both in vitro and in vivo (P<0.01), as compared with the TFO‑M, TFO+U and SSRE groups. The UTMD‑based TFO delivery system promoted the -absorption of TFO and the inhibition of TF, and was therefore considered to be favorable for preventing thrombosis induced by shear stress.
三链形成寡脱氧核苷酸(TFO)的细胞摄取效率以及对组织因子(TF)的抑制作用较低。本研究的目的是通过使用基于超声靶向微泡破坏(UTMD)的递送系统,提高TFO的吸收,并在体外和体内增强对剪切应力诱导的TF的抑制作用。首先构建并表征了TFO偶联脂质超声微泡(TFO-M)。通过基于荧光的方法观察TFO的吸收情况,并通过免疫荧光和定量聚合酶链反应检测TF的抑制情况。用未超声处理的TFO偶联脂质超声微泡处理后,对ECV304人脐静脉内皮细胞施加6小时的流体剪切应力(TFO-M组);单独使用TFO;TFO偶联脂质超声微泡,外加即时超声处理(TFO+U组和TFO-M+U组);或仅用0.9%氯化钠进行模拟处理(SSRE组)。体内实验的设置与体外实验类似,只是将TFO或TFO-M通过尾静脉注射到大鼠体内。在制备颈动脉狭窄模型6小时后,对大鼠实施安乐死。与TFO-M组和TFO+U组相比,TFO-M+U组中TFO的转染效率更高(P<0.01)。与TFO-M组、TFO+U组和SSRE组相比,TFO-M+U组中TF的蛋白质和mRNA表达在体外和体内均显著降低(P<0.01)。基于UTMD的TFO递送系统促进了TFO的吸收和对TF的抑制,因此被认为有利于预防剪切应力诱导的血栓形成。