Long-term expression of foreign genes in normal human epidermal keratinocytes after transfection with lipid/DNA complexes

被引:36
作者
Zellmer, S
Gaunitz, F
Salvetter, J
Surovoy, A
Reissig, D
Gebhardt, R
机构
[1] Univ Leipzig, Fac Med, Inst Biochem, D-04103 Leipzig, Germany
[2] Univ Leipzig, Fac Med, Inst Anat, D-04103 Leipzig, Germany
[3] Russian Acad Sci, Inst Bioorgan Chem, Moscow 117871, Russia
关键词
cationic lipids; transplantation; air-liquid interface culture; serum-free;
D O I
10.1007/s004180000225
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Normal human epidermal keratinocytes were isolated and cultivated in scrum-free medium. The expression of the integrin subunits alpha (6) and beta (1) indicated that a high number of keratinocytes from the stem cell system was present. These cells were transfected with complexes made of different cationic lipids and marker genes. Effectene showed a 20-fold higher transfection efficiency, compared to Lipofectin and Lipofectamine, and a similar low toxicity. The transfection protocol was optimised. A DNA/lipid ratio of 0.133 showed the highest transfection efficiency. Keratinocytes expressed the marker gene luciferase for 20 days. The maximum expression occurred after 3-4 days, where individual patches of fluorescent keratinocytes were detected. Transfected keratinocytes, cultivated at the air-liquid interface, expressed the marker gene beta -galactosidase for at least 7 weeks.
引用
收藏
页码:41 / 47
页数:7
相关论文
共 27 条
[1]   3 CLONAL TYPES OF KERATINOCYTE WITH DIFFERENT CAPACITIES FOR MULTIPLICATION [J].
BARRANDON, Y ;
GREEN, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (08) :2302-2306
[2]   CELL-SIZE AS A DETERMINANT OF THE CLONE-FORMING ABILITY OF HUMAN KERATINOCYTES [J].
BARRANDON, Y ;
GREEN, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (16) :5390-5394
[3]   Efficient gene transfer into human keratinocytes with recombinant adeno-associated virus vectors [J].
Braun-Falco, M ;
Doenecke, A ;
Smola, H ;
Hallek, M .
GENE THERAPY, 1999, 6 (03) :432-441
[4]   Transglutaminase 1 delivery to lamellar ichthyosis keratinocytes [J].
Choate, KA ;
Kinsella, TM ;
Williams, ML ;
Nolan, GP ;
Khavari, PA .
HUMAN GENE THERAPY, 1996, 7 (18) :2247-2253
[5]   THE FATE OF GENETICALLY MARKED HUMAN ORAL KERATINOCYTES IN-VITRO [J].
GARLICK, JA ;
TAICHMAN, LB .
ARCHIVES OF ORAL BIOLOGY, 1993, 38 (10) :903-910
[6]   Expression of naked DNA in human, pig, and mouse skin [J].
Hengge, UR ;
Walker, PS ;
Vogel, JC .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (12) :2911-2916
[7]   CYTOKINE GENE-EXPRESSION IN EPIDERMIS WITH BIOLOGICAL EFFECTS FOLLOWING INJECTION OF NAKED DNA [J].
HENGGE, UR ;
CHAN, EF ;
FOSTER, RA ;
WALKER, PS ;
VOGEL, JC .
NATURE GENETICS, 1995, 10 (02) :161-166
[8]   Efficient in vitro transfection of human keratinocytes with an adenovirus-enhanced receptor-mediated system [J].
Huber, M ;
Limat, A ;
Wagner, E ;
Hohl, D .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 114 (04) :661-666
[9]   Isolation and characterization of human epidermal stem cells [J].
Jones, PH .
CLINICAL SCIENCE, 1996, 91 (02) :141-146
[10]   Adhesive properties of human basal epidermal cells: An analysis of keratinocyte stem cells, transit amplifying cells, and postmitotic differentiating cells [J].
Kaur, P ;
Li, A .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 114 (03) :413-420