Fetal gene transfer by transuterine injection of cationic liposome-DNA complexes

被引:29
作者
Gaensler, KML [1 ]
Tu, GH
Bruch, S
Liggitt, D
Lipshutz, GS
Metkus, A
Harrison, M
Heath, TD
Debs, RJ
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[2] Calif Pacific Med Ctr, Inst Res, San Francisco, CA 94115 USA
[3] Univ Calif San Francisco, Dept Surg, San Francisco, CA 94143 USA
[4] Univ Washington, Dept Comparat Med, Seattle, WA 98195 USA
[5] Univ Wisconsin, Sch Pharm, Madison, WI 53706 USA
关键词
gene therapy; gene transfer; cationic liposomes; fetus; in utero;
D O I
10.1038/70729
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
In utero injection of cationic liposome-DNA complexes (CLDCs) containing chloramphenicol acetyltransferase, beta-galactosidase (beta-gal), or human granulocyte colony-stimulating factor (hG-CSF) expression plasmids produced high-level gene expression in fetal rats. Tissues adjacent to the injection site exhibited the highest levels of gene expression. Chloramphenicol acetyltransferase expression persisted for at least 14 days and was reexpressed following postnatal reinjection of CLDCs. Intraperitoneal administration of the hG-CSF gene produced high serum hG-CSF levels. X-gal staining demonstrated widespread beta-gal expression in multiple fetal tissues and cell types. No toxic or inflammatory responses were observed, nor was there evidence of fetal-maternal or maternal-fetal gene transfer, suggesting that CLDCs may provide a useful alternative to viral vectors for in utero gene transfer.
引用
收藏
页码:1188 / 1192
页数:5
相关论文
共 50 条
[1]   NONINVASIVE LIPOSOME-MEDIATED GENE DELIVERY CAN CORRECT THE ION-TRANSPORT DEFECT IN CYSTIC-FIBROSIS MUTANT MICE [J].
ALTON, EWFW ;
MIDDLETON, PG ;
CAPLEN, NJ ;
SMITH, SN ;
STEEL, DM ;
MUNKONGE, FM ;
JEFFERY, PK ;
GEDDES, DM ;
HART, SL ;
WILLIAMSON, R ;
FASOLD, KI ;
MILLER, AD ;
DICKINSON, P ;
STEVENSON, BJ ;
MCLACHLAN, G ;
DORIN, JR ;
PORTEOUS, DJ .
NATURE GENETICS, 1993, 5 (02) :135-142
[2]  
BARTKE A, 1994, P SOC EXP BIOL MED, V206, P345, DOI 10.3181/00379727-206-43771
[3]   INVIVO TRANSFER AND EXPRESSION OF THE LACZ GENE IN THE MOUSE LUNG [J].
BOUT, A ;
VALERIO, D ;
SCHOLTE, BJ .
EXPERIMENTAL LUNG RESEARCH, 1993, 19 (02) :193-202
[4]   NO LUNG TOXICITY AFTER REPEATED AEROSOL OR INTRAVENOUS DELIVERY OF PLASMID-CATIONIC LIPOSOME COMPLEXES [J].
CANONICO, AE ;
PLITMAN, JD ;
CONARY, JT ;
MEYRICK, BO ;
BRIGHAM, KL .
JOURNAL OF APPLIED PHYSIOLOGY, 1994, 77 (01) :415-419
[5]   AEROSOL AND INTRAVENOUS TRANSFECTION OF HUMAN ALPHA-1-ANTITRYPSIN GENE TO LUNGS OF RABBITS [J].
CANONICO, AE ;
CONARY, JT ;
MEYRICK, BO ;
BRIGHAM, KL .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1994, 10 (01) :24-29
[6]   FETAL LIVER HEMATOPOIETIC STEM-CELLS AS A TARGET FOR INUTERO RETROVIRAL GENE-TRANSFER [J].
CLAPP, DW ;
DUMENCO, LL ;
HATZOGLOU, M ;
GERSON, SL .
BLOOD, 1991, 78 (04) :1132-1139
[7]   Safety-modified episomal vectors for human gene therapy [J].
Cooper, MJ ;
Lippa, M ;
Payne, JM ;
Hatzivassiliou, G ;
Reifenberg, E ;
Fayazi, B ;
Perales, JC ;
Morrison, LJ ;
Templeton, D ;
Piekarz, RL ;
Tan, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (12) :6450-6455
[8]   PROLONGED TRANSGENE EXPRESSION IN RODENT LUNG-CELLS [J].
DEBS, R ;
PIAN, M ;
GAENSLER, K ;
CLEMENTS, J ;
FRIEND, DS ;
DOBBS, L .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1992, 7 (04) :406-413
[9]   TOTIPOTENT HEMATOPOIETIC STEM-CELLS - NORMAL SELF-RENEWAL AND DIFFERENTIATION AFTER TRANSPLANTATION BETWEEN MOUSE FETUSES [J].
FLEISCHMAN, RA ;
CUSTER, RP ;
MINTZ, B .
CELL, 1982, 30 (02) :351-359
[10]   GERM-LINE TRANSMISSION AND DEVELOPMENTAL REGULATION OF A 150-KB YEAST ARTIFICIAL CHROMOSOME CONTAINING THE HUMAN BETA-GLOBIN LOCUS IN TRANSGENIC MICE [J].
GAENSLER, KML ;
KITAMURA, M ;
KAN, YW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (23) :11381-11385