Fetal gene transfer by intrauterine injection with microbubble-enhanced ultrasound

被引:80
作者
Endoh, M
Koibuchi, N
Sato, M
Morishita, R
Kanzaki, T
Murata, Y
Kaneda, Y
机构
[1] Osaka Univ, Sch Med, Dept Gene Therapy Sci, Suita, Osaka 565, Japan
[2] Osaka Univ, Sch Med, Dept Obstet & Gynecol, Suita, Osaka 565, Japan
关键词
gene transfer; in vivo delivery; naked DNA; ultrasound; in utero; oligodeoxynucleotide; microbubble; gene therapy;
D O I
10.1006/mthe.2002.0577
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Intrauterine injection of naked DNA expressing luciferase, green fluorescent protein (GFP), or beta-galactosidase (beta-gal) and fluorescein isothiocyanate-labeled oligodeoxynucleotide (FITC-ODN), in combination with microbubble-enhanced ultrasound (US), referred to as the "shot-gun method" (SGM), produced high-level protein expression in fetal mice. With the SGM, luciferase expression increased similar to10(3)-fold in comparison with expression after injection of naked DNA alone. Electron microscopic analysis demonstrated transient formation of pores on the skin surface after intraamniotic (i.a.) injection with the SGM. Widespread expression of GFP and beta-gal and delivery of FITC-ODN were observed in multiple fetal tissues adjacent to the injection points. PCR analysis indicated that germline transfection was only transient following intraperitoneal (i.p) injection, and there was no evidence of transfer of the reporter gene to the offspring. Thus, SGM might provide a useful means to clarify the molecular mechanisms of genetic diseases in utero, as well as a tool to develop gene therapies in utero.
引用
收藏
页码:501 / 508
页数:8
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