中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2014年
18期
2801-2805
,共5页
孙玉梅%张金盈%闫继锋%袁斌%杨鹏伟%李文%于运福
孫玉梅%張金盈%閆繼鋒%袁斌%楊鵬偉%李文%于運福
손옥매%장금영%염계봉%원빈%양붕위%리문%우운복
动物模型%组织工程%RNA干扰%短发卡样RNA%骨桥蛋白%再狭窄%基因治疗%动脉粥样硬化%血管成形%平滑肌细胞
動物模型%組織工程%RNA榦擾%短髮卡樣RNA%骨橋蛋白%再狹窄%基因治療%動脈粥樣硬化%血管成形%平滑肌細胞
동물모형%조직공정%RNA간우%단발잡양RNA%골교단백%재협착%기인치료%동맥죽양경화%혈관성형%평활기세포
atherosclerosis%coronary artery disease%RNA interference%osteopontin%myocytes%smooth muscle
背景:血管成形后再狭窄严重限制了经皮冠状动脉介入治疗的应用和远期疗效。平滑肌细胞的表型转变,增殖是血管成形后再狭窄的重要机制。<br> 目的:探讨利用球囊在体转导骨桥蛋白短发夹状RNA,通过抑制实验性动脉粥样硬化模型兔损伤血管部位骨桥蛋白的表达,预防血管成形后再狭窄。<br> 方法:构建动脉粥样硬化模型兔20只,随机等分成空质粒组和OPN-shRNA质粒组,分别利用球囊在腹主动脉导入OPN-shRNA质粒和空载体。<br> 结果与结论:2组兔球囊扩张后血管平滑肌层出现特异性绿色荧光,且随转染后时间的延长荧光强度逐渐降低,与空质粒组相比,OPN-shRNA 质粒组兔扩张动脉的管腔面积明显增加,而斑块负荷明显减小。提示在动脉粥样硬化兔模型局部血管利用球囊导管能成功地转导OPN-shRNA质粒,被扩张血管的再狭窄程度减轻,血栓负荷减轻。这对于预防模型兔血管成形后再狭窄的发生具有十分重要的意义。
揹景:血管成形後再狹窄嚴重限製瞭經皮冠狀動脈介入治療的應用和遠期療效。平滑肌細胞的錶型轉變,增殖是血管成形後再狹窄的重要機製。<br> 目的:探討利用毬囊在體轉導骨橋蛋白短髮夾狀RNA,通過抑製實驗性動脈粥樣硬化模型兔損傷血管部位骨橋蛋白的錶達,預防血管成形後再狹窄。<br> 方法:構建動脈粥樣硬化模型兔20隻,隨機等分成空質粒組和OPN-shRNA質粒組,分彆利用毬囊在腹主動脈導入OPN-shRNA質粒和空載體。<br> 結果與結論:2組兔毬囊擴張後血管平滑肌層齣現特異性綠色熒光,且隨轉染後時間的延長熒光彊度逐漸降低,與空質粒組相比,OPN-shRNA 質粒組兔擴張動脈的管腔麵積明顯增加,而斑塊負荷明顯減小。提示在動脈粥樣硬化兔模型跼部血管利用毬囊導管能成功地轉導OPN-shRNA質粒,被擴張血管的再狹窄程度減輕,血栓負荷減輕。這對于預防模型兔血管成形後再狹窄的髮生具有十分重要的意義。
배경:혈관성형후재협착엄중한제료경피관상동맥개입치료적응용화원기료효。평활기세포적표형전변,증식시혈관성형후재협착적중요궤제。<br> 목적:탐토이용구낭재체전도골교단백단발협상RNA,통과억제실험성동맥죽양경화모형토손상혈관부위골교단백적표체,예방혈관성형후재협착。<br> 방법:구건동맥죽양경화모형토20지,수궤등분성공질립조화OPN-shRNA질립조,분별이용구낭재복주동맥도입OPN-shRNA질립화공재체。<br> 결과여결론:2조토구낭확장후혈관평활기층출현특이성록색형광,차수전염후시간적연장형광강도축점강저,여공질립조상비,OPN-shRNA 질립조토확장동맥적관강면적명현증가,이반괴부하명현감소。제시재동맥죽양경화토모형국부혈관이용구낭도관능성공지전도OPN-shRNA질립,피확장혈관적재협착정도감경,혈전부하감경。저대우예방모형토혈관성형후재협착적발생구유십분중요적의의。
BACKGROUND:Restenosis after angioplasty severely limited the application and long-period therapeutic effects of percutaneous coronary intervention. Changes in smooth muscle cel phenotype and their proliferation are important mechanisms of restenosis after angioplasty. <br> OBJECTIVE:To use bal oon in vivo transduction of osteopontin short hairpin RNA (OPN-shRNA), to inhibit osteopontin expression at the injured blood vessels of a rabbit model of experimental atherosclerosis, and to prevent restenosis after angioplasty. <br> METHODS:A total of 20 rabbit models of atherosclerosis were established and randomly equal y assigned to empty plasmid group and OPN-shRNA plasmid group. The plasmid recombinant OPN-shRNA and empty plasmid were transferred to the ventral aorta by bal oon. <br> RESULTS AND CONCLUSION:After bal oon dilatation, specific green fluorescence was detected in the layer of vascular smooth muscle in the two groups. Moreover, with prolonged time of transfection, fluorescence intensity gradual y decreased. Compared with the empty plasmid group, the expanded artery lumen area obviously increased in the OPN-shRNA plasmid group, and plaque burden evidently reduced. Results indicated that bal oon catheter used in regional blood vessels in rabbit models of atherosclerosis could successful y transduce OPN-shRNA plasmid. The restenosis of the expanded blood vessels lessened, and thrombus burden relieved. It is of great importance to prevent the occurrence of restenosis after angioplasty in rabbit models.