Gene transfer into porcine myocardium via pericardial cavity by homemade easy puncture device.

Huai-Min Guan, Peng Liu, Jin-Hong Xie, Feng-Ling Wang, Lin-Sheng Cao, Qi-Jun Qian
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Abstract

Objective: To explore the feasibility and safety of gene transfer into porcine myocardium via the pericardial cavity by a homemade easy device.

Methods: Replication-deficient recombinant adenoviral vector carrying LacZ report gene (Ad-LacZ) was constructed by the calcium phosphate precipitation method. Twelve healthy Chinese mini-swine were randomly divided into experimental group (n = 6) and control group (n = 6). Acute myocardial infarction (AMI) model was established by balloon occlusion of the distal part of D1 branch of left anterior descending (LAD) artery, at the same time the intrapericardial cavity injections were performed through the small incision of the abdominal wall below the xyphoid appendix using a homemade device. Then gene transfer was performed using a central venous catheter. The pericardium was pretreated with injection of a mixture of collagenase (1,200 U) and hyaluronidase (3,000 U) in both groups. Then 2.0 x 10(9) plaque formation unit (PFU) Ad-LacZ was injected into the pericardial cavity in experimental group, while 1 mL of normal saline was injected in the control group. The beta-galactosidase activity detection and X-gal staining of the ischemic myocardium were performed on the 3rd, 7th, and 28th day after injection.

Results: The LAD artery was occluded completely and infarction and ischemia were detected by histological assessment In experimental group, the X-gal staining positive cells and beta-galactosidase activity quantification were detectable on the 3rd day after injection, increased markedly on the 7th day, and then declined on the 28th day. The transfer efficiencies indicated by the positive myocardial cells were 16.7%, 45.6% , 22.8% on the 3rd, 7th, 28th day, respectively. In control group, no positive cells and beta-galactosidase activity were observed.

Conclusion: Adenovirus can be transferred into ischemic myocardium and express target gene in the AMI model for four weeks with the homemade easy device via pericardial cavity pretreated by collagenase and hyaluronidase.

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自制简易穿刺装置经心包腔将基因转入猪心肌。
目的:探讨自制简易装置经心包腔向猪心肌内转移基因的可行性和安全性。方法:采用磷酸钙沉淀法构建携带LacZ报告基因的复制缺陷重组腺病毒载体(Ad-LacZ)。选取健康中国小型猪12头,随机分为实验组(n = 6)和对照组(n = 6),采用球囊闭塞左前降支(LAD)远端部分建立急性心肌梗死(AMI)模型,同时采用自制器械经椎弓形尾突下方腹壁小切口心包腔内注射。然后通过中心静脉导管进行基因转移。两组心包均注射胶原酶(1200 U)和透明质酸酶(3000 U)混合液预处理。实验组在心包腔内注射2.0 × 10(9) PFU的Ad-LacZ,对照组注射生理盐水1 mL。注射后第3、7、28天对缺血心肌进行β -半乳糖苷酶活性检测和X-gal染色。结果:LAD动脉完全闭塞,组织学检查可见梗死和缺血。实验组注射后第3天检测到X-gal染色阳性细胞和β -半乳糖苷酶活性定量,第7天明显升高,第28天下降。第3天、第7天、第28天心肌细胞转染效率分别为16.7%、45.6%、22.8%。对照组无阳性细胞,无-半乳糖苷酶活性。结论:用自制简易装置经胶原酶和透明质酸酶预处理心包腔,可将腺病毒转染缺血心肌,并在心肌梗死模型中表达靶基因4周。
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