Stable gene transfer and expression in human primary T cells by the Sleeping Beauty transposon system

被引:81
作者
Huang, X
Wilber, AC
Bao, L
Tuong, D
Tolar, J
Orchard, PJ
Levine, BL
June, CH
McIvor, RS
Blazar, BR
Zhou, XZ
机构
[1] Univ Minnesota, Ctr Canc, Div Blood & Marrow Transplantat, Dept Pediat, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Ctr Canc, Dept Genet Cell Biol & Dev, Minneapolis, MN 55455 USA
[3] Univ Penn, Dept Pathol & Lab Med, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
关键词
D O I
10.1182/blood-2005-05-2133
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Sleeping Beauty (SB)transposon system is a nonviral DNA delivery system in which a transposase directs integration of an SB transposon into TA-dinucleotide sites in the genome. To determine whether the SB transposon system can mediate stable gene expression in human T cells, primary peripheral blood lymphocytes (PBLs) were nucleofected with SB vectors carrying a DsRed reporter gene. Plasmids containing the SB transposase on the same molecule as (cis) or on a molecule separate from (trans)the SB transposon mediated long-term and stable reporter gene expression in human primary T cells. Sequencing of transposon:chromosome junctions confirmed that stable gene expression was due to SB-mediated transposition. In other studies, PBLs were successfully transfected using the SB transposon system and shown to stably express a fusion protein consisting of (1) a surface receptor useful for positive T-cell selection and (2) a '' suicide '' gene useful for elimination of transfected T cells after chemotherapy. This study is the first report demonstrating that the SB transposon system can mediate stable gene transfer in human primary PBLs, which may be advantageous for T-cell-based gene therapies.
引用
收藏
页码:483 / 491
页数:9
相关论文
共 55 条
[11]   Structure-function analysis of the inverted terminal repeats of the Sleeping Beauty transposon [J].
Cui, ZB ;
Geurts, AM ;
Liu, GY ;
Kaufman, CD ;
Hackett, PB .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 318 (05) :1221-1235
[12]   Expression of Bcl-XL restores cell survival, but not proliferation and effector differentiation, in CD28-deficient T lymphocytes [J].
Dahl, AM ;
Klein, C ;
Andres, PG ;
London, CA ;
Lodge, MP ;
Mulligan, RC ;
Abbas, AK .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (12) :2031-2037
[13]   Gene therapy insertional mutagenesis insights [J].
Davé, UP ;
Jenkins, NA ;
Copeland, NG .
SCIENCE, 2004, 303 (5656) :333-333
[14]   Targeting of proteins derived from self-processing polyproteins containing multiple signal sequences [J].
de Felipe, P ;
Ryan, MD .
TRAFFIC, 2004, 5 (08) :616-626
[15]   TCR analysis reveals significant repertoire selection during in vitro lymphocyte culture [J].
Dietrich, PY ;
Walker, PR ;
Schnuriger, V ;
Saas, P ;
Perrin, G ;
Guillard, M ;
Gaudin, C ;
Caignard, A .
INTERNATIONAL IMMUNOLOGY, 1997, 9 (08) :1073-1083
[16]   Mammalian germ-line transgenesis by transposition [J].
Dupuy, AJ ;
Clark, K ;
Carlson, CM ;
Fritz, S ;
Davidson, AE ;
Markley, KM ;
Finley, K ;
Fletcher, CF ;
Ekker, SC ;
Hackett, PB ;
Horn, S ;
Largaespada, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (07) :4495-4499
[17]   Retrovirus-mediated gene transfer in primary T lymphocytes:: Influence of the transduction/selection process and of ex vivo expansion on the T cell receptor β chain hypervariable region repertoire [J].
Ferrand, C ;
Robinet, E ;
Contassot, E ;
Certoux, JM ;
Lim, A ;
Hervé, P ;
Tiberghien, P .
HUMAN GENE THERAPY, 2000, 11 (08) :1151-1164
[18]   Gene therapy of severe combined immunodeficiencies [J].
Fischer, A ;
Hacein-Bey, S ;
Cavazzana-Calvo, M .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (08) :615-621
[19]   Cellular fate of a modular DNA delivery system mediated by silica nanoparticles [J].
Gemeinhart, RA ;
Luo, D ;
Saltzman, WM .
BIOTECHNOLOGY PROGRESS, 2005, 21 (02) :532-537
[20]   Gene transfer into genomes of human cells by the sleeping beauty transposon system [J].
Geurts, AM ;
Yang, Y ;
Clark, KJ ;
Liu, GY ;
Cui, ZB ;
Dupuy, AJ ;
Bell, JB ;
Largaespada, DA ;
Hackett, PB .
MOLECULAR THERAPY, 2003, 8 (01) :108-117