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CD151基因治疗改善小型猪心肌梗死后心功能的研究
引用本文:左后娟,刘正湘,刘晓春,曾和松,文莎,刘涛,汪道文.CD151基因治疗改善小型猪心肌梗死后心功能的研究[J].中华老年医学杂志,2009,28(9).
作者姓名:左后娟  刘正湘  刘晓春  曾和松  文莎  刘涛  汪道文
作者单位:1. 华中科技大学同济医学院附属同济医院心内科,武汉,430030
2. 华中科技大学同济医学院神经生物学系
摘    要:目的 研究重组腺相关病毒(rAAV)介导的CD151基因转染小型猪心肌梗死模型对心肌梗死后心功能的影响,以明确CD151体内促血管新生的作用.方法 实验用小型猪分为4组:(1)正常对照组4只;(2)rAAV-含绿色荧光蛋白序列(GFP)组6只;(3)rAAV-CD151组6只;rAAV-antiCD151组6只.结扎猪冠状动脉左前降支建立心肌梗死模型.包装正义及反义CD151腺相关病毒,分点注射至梗死区及梗死周围心肌进行基因转染.基因转染8周行Westernblot测定心肌组织CD151蛋白表达,氮-13-氨水(13N-NH3)电子发射计算机断层显影(PET)评价心肌血流灌注,超声心动图检测心功能.结果 CD151基因转染促进心肌组织局部CD151高表达.与rAAV-GFP组比较,基因转染8周时rAAV-CD151组心肌缺损面积减小(11.3±2.4)%与(21.1±2.6)%,t=-5.67,P<0.01],心功能各指标左心室射血分数(65.7±4.6)%与(54.7±5.3)%,t=3.98,P<0.05]、左心室短轴缩短率(36.0±2.9)%与(27.6±3.1)%,t=3.35,P<0.05]、左心室前侧壁的增厚率(55.4±4.9)%与(36.8±7.8)%,t=3.34,P<0.05]和室间隔的增厚率(35.2±6.0)%与(26.7±4.4)%,t=9.27,P<0.01]均增加,左心室前侧壁和室间隔的厚度亦增加(P<0.05).rAAV-antiCD151组各参数则低于rAAV-CD151组(均P<0.05).结论 rAAV-CD151能有效转染小型猪心肌,增加缺血心肌血流灌注,减小梗死面积,明显增加心肌收缩力并改善心功能.

关 键 词:转染  基因疗法  心肌梗死  

Experimental study of CD151 gene therapy on improving myocardial function in swines with myocardial infarction
ZUO Hou-juan,LIU Zheng-xiang,LIU Xiao-chun,ZENG He-song,WEN Sha,LIU Tao,WANG Dao-wen.Experimental study of CD151 gene therapy on improving myocardial function in swines with myocardial infarction[J].Chinese Journal of Geriatrics,2009,28(9).
Authors:ZUO Hou-juan  LIU Zheng-xiang  LIU Xiao-chun  ZENG He-song  WEN Sha  LIU Tao  WANG Dao-wen
Abstract:Objective To investigate the effect of CD151 gene therapy on improving myocardial function in swines with myocardial infarction. Methods CD151, antisense CD151 and green fluorescent protein (GFP) were constructed into the recombinant adeno-associated virus (rAAV). Swines were divided into 4 groups: rAAV-GFP group (6 swines), rAAV-CD151 group (6 swines), rAAV-antiCD151 group (6 swines) and control group (6 swines). The swines were performed with coronary artery ligation and intramuscularly injection with rAAV. Eight weeks after vector administration, western blot was used to detect gene expression of CD151. 13N-labeled NH3 positron emission tomography (PET) was used to evaluate myocardial perfusion. Echocardiography was used to assess myocardial function. Results Compared with the control group and the rAAV-GFP group, the rAAV-CD151 group showed higher CD151 protein expression. Compared with the rAAV-GFP group, the defect size of myocardium was decreased( 11.3±2.4)% vs. (21.1±2.6)%, t= -5.67,P<0.01] and left ventricular ejection fraction (EF), left ventricular fractional shortening (FS), the ratio of anterior lateral wall thickening (△ALWT) and ratio of interventricular septum thickening (△IVST) were significantly improved in rAAV-CD151 group 8 weeks after vector administration (65.7±4.6)% vs. (54.7±5.3)%, (36.0±2.9)% vs. (27.6±3.1)%,(55.4± 4.9)% vs. (36.8±7.8)%, (35.2±6.0)% vs. (26.7±4.4)%, t=3.98, 3.35, 3.34, 9.27, all P< 0.05]. The level of diastolic ALWT and diastolic IVST was also increased in rAAV CD151 group compared with rAAV-GFP group ( P<0.05).Compared with rAAV-CD151 group, parameters of myocardial function in rAAV-antisense CD151 group were not improved (P<0.05). Conclusions rAAV-CD151 can effectively transfeet the myocardium, increase the expression ofCD151 protein, promote the blood perfusion of myocardium and improve the ventricular function after myocardial infarction.
Keywords:Transfection  Gene therapy  Myocardial infarction  Swine
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