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通过小脂质体将基因体内转移至肝细胞后,人α1 -抗胰蛋白酶在小鼠体内的表达。

Expression of human alpha 1-antitrypsin in mouse after in vivo gene transfer to hepatocytes by small liposomes.

作者信息

Aliño S F, Crespo J, Bobadilla M, Lejarreta M, Blaya C, Crespo A

机构信息

Department of Pharmacology, Faculty of Medicine and Dentistry, University of Valencia, Spain.

出版信息

Biochem Biophys Res Commun. 1994 Nov 15;204(3):1023-30. doi: 10.1006/bbrc.1994.2565.

Abstract

A plasmid (pTG7101) containing the full-length human alpha 1-antitrypsin gene was encapsulated in small liposomes and used for "in vivo" gene transfer to mouse hepatocytes, by i.v. injection (100 ng DNA/mouse and dose). The expression of human protein was evaluated by microspectrophotometry after human alpha 1-antitrypsin immunoperoxidase reaction on liver cryosections and the presence in mouse plasma of de novo synthesized protein was detected by ELISA analysis. Our results indicate that a single dose of encapsulated plasmid induces the expression of human alpha 1-antitrypsin in mouse hepatocytes and a large effect (70%) remains two weeks after treatment. However, no effect was observed when mice were treated with buffer or free plasmid (100 ng/mouse) plus an equivalent lipid dose of empty liposomes. In addition, whereas no additive effect was observed after repetitive treatment-doses, the partial hepatectomy three hours after a single treatment-dose, significantly increased the presence of human alpha 1-antitrypsin in mice plasma.

摘要

将含有全长人α1-抗胰蛋白酶基因的质粒(pTG7101)包裹于小脂质体中,通过静脉注射(100 ng DNA/小鼠及剂量)用于对小鼠肝细胞进行“体内”基因转移。在肝脏冰冻切片上进行人α1-抗胰蛋白酶免疫过氧化物酶反应后,通过显微分光光度法评估人蛋白的表达,并通过ELISA分析检测小鼠血浆中新生合成蛋白的存在。我们的结果表明,单剂量的包裹质粒可诱导小鼠肝细胞中人α1-抗胰蛋白酶的表达,且在治疗后两周仍有显著效果(70%)。然而,当用缓冲液或游离质粒(100 ng/小鼠)加等量脂质剂量的空脂质体处理小鼠时,未观察到效果。此外,重复给药后未观察到累加效应,但单次给药后三小时进行部分肝切除术,可显著增加小鼠血浆中人α1-抗胰蛋白酶的含量。

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