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
12期
1926-1931
,共6页
王珏%王竞男%邓宇斌%杨立群
王玨%王競男%鄧宇斌%楊立群
왕각%왕경남%산우빈%양립군
生物材料%纳米材料%基因运载载体%支链淀粉衍生物%颈动脉注射%尾静脉注射%绿色荧光蛋白%基因转染%脑卒中
生物材料%納米材料%基因運載載體%支鏈澱粉衍生物%頸動脈註射%尾靜脈註射%綠色熒光蛋白%基因轉染%腦卒中
생물재료%납미재료%기인운재재체%지련정분연생물%경동맥주사%미정맥주사%록색형광단백%기인전염%뇌졸중
biocompatible materials%carotid arteries%injections,intra-arterial%green fluorescent proteins%transfection
背景:超支化支链淀粉衍生物作为非病毒基因载体具有低毒性、转染率好的特点,但如何高效递送其进入机体内使有治疗作用基因成功表达的方式仍在探索中。<br> 目的:探讨包裹绿色荧光蛋白的新型基因运载载体经改进颈动脉注射法到达大鼠脑缺血损伤区的表达情况。方法:取雄性SD大鼠制作大脑中动脉梗死模型,24 h后随机分为2组,对照组以尾静脉注射包裹绿色荧光蛋白的超支化支链淀粉衍生物,实验组以改进型颈内动脉注射包裹绿色荧光蛋白的超支化支链淀粉衍生物。7 d后处死大鼠,取出脑组织,qPCR和Western blot检测大鼠脑组织中绿色荧光蛋白的基因和蛋白水平,免疫荧光法观察脑组织冰冻切片中血管内壁附近绿色荧光蛋白的表达。<br> 结果与结论:qPCR和Western blot检测结果均显示实验组大鼠脑组织中绿色荧光蛋白的表达量显著高于对照组(P<0.05),免疫荧光观察结果显示绿色荧光蛋白在实验组血管内壁附近的表达高于对照组。在SD大鼠大脑中动脉梗死模型中,相比尾静脉注射法,改进型颈动脉注射法可显著促进脑缺血损伤区的超支化支链淀粉衍生物及绿色荧光蛋白在脑组织中表达的量。
揹景:超支化支鏈澱粉衍生物作為非病毒基因載體具有低毒性、轉染率好的特點,但如何高效遞送其進入機體內使有治療作用基因成功錶達的方式仍在探索中。<br> 目的:探討包裹綠色熒光蛋白的新型基因運載載體經改進頸動脈註射法到達大鼠腦缺血損傷區的錶達情況。方法:取雄性SD大鼠製作大腦中動脈梗死模型,24 h後隨機分為2組,對照組以尾靜脈註射包裹綠色熒光蛋白的超支化支鏈澱粉衍生物,實驗組以改進型頸內動脈註射包裹綠色熒光蛋白的超支化支鏈澱粉衍生物。7 d後處死大鼠,取齣腦組織,qPCR和Western blot檢測大鼠腦組織中綠色熒光蛋白的基因和蛋白水平,免疫熒光法觀察腦組織冰凍切片中血管內壁附近綠色熒光蛋白的錶達。<br> 結果與結論:qPCR和Western blot檢測結果均顯示實驗組大鼠腦組織中綠色熒光蛋白的錶達量顯著高于對照組(P<0.05),免疫熒光觀察結果顯示綠色熒光蛋白在實驗組血管內壁附近的錶達高于對照組。在SD大鼠大腦中動脈梗死模型中,相比尾靜脈註射法,改進型頸動脈註射法可顯著促進腦缺血損傷區的超支化支鏈澱粉衍生物及綠色熒光蛋白在腦組織中錶達的量。
배경:초지화지련정분연생물작위비병독기인재체구유저독성、전염솔호적특점,단여하고효체송기진입궤체내사유치료작용기인성공표체적방식잉재탐색중。<br> 목적:탐토포과록색형광단백적신형기인운재재체경개진경동맥주사법도체대서뇌결혈손상구적표체정황。방법:취웅성SD대서제작대뇌중동맥경사모형,24 h후수궤분위2조,대조조이미정맥주사포과록색형광단백적초지화지련정분연생물,실험조이개진형경내동맥주사포과록색형광단백적초지화지련정분연생물。7 d후처사대서,취출뇌조직,qPCR화Western blot검측대서뇌조직중록색형광단백적기인화단백수평,면역형광법관찰뇌조직빙동절편중혈관내벽부근록색형광단백적표체。<br> 결과여결론:qPCR화Western blot검측결과균현시실험조대서뇌조직중록색형광단백적표체량현저고우대조조(P<0.05),면역형광관찰결과현시록색형광단백재실험조혈관내벽부근적표체고우대조조。재SD대서대뇌중동맥경사모형중,상비미정맥주사법,개진형경동맥주사법가현저촉진뇌결혈손상구적초지화지련정분연생물급록색형광단백재뇌조직중표체적량。
BACKGROUND:Hyperbranched cationic amylopectin is a kind of nonviral gene vectors with low toxicity and good transfection efficiency. However, searching for more efficient methods to delivery it into the body and making the genes expressed are being explored. <br> OBJECTIVE:To study the expression of DMAPA-Amp wrapped green fluorescent protein (GFP) transferred by modified carotid injection into cerebral ischemic area. <br> METHODS:Male Sprague-Dawley rats subjected to middle cerebral artery infarction were randomly divided into two groups after 24 hours:experimental group (injected with GFP entrapped DMAPA-Amp via the internal carotid artery) and control group (injected with GFP entrapped DMAPA-Amp via the tail vein). These rats were put to death and their brain tissue was removed after 7 days. The expression of GFP was detected by quantitative PCR and western blot assay, and immunofluorescence staining was performed to detect the expression of GFP located near cerebrovascular endothelial cel s by frozen section. <br> RESULTS AND CONCLUSION:Compared with the control group, the expression of GFP was much higher in the experimental group detected by quantitative PCR and western blot (P< 0.05). Additional y, the expression of GFP located near cerebrovascular endothelial cel s by frozen section was also higher than that in the control group. Modified carotid injection could significantly promote the expression of hyperbranched cationic amylopectin derivates and GFP in the brain tissue of Sprague-Dawley rats undergoing middle cerebral artery infarction compared with tail vein injection, which indicates DMAPA-Amp and modified carotid injection may cast new lights on the therapy for angiogenesis of ischemic stroke.