Gas-inducible transgene expression in mammalian cells and mice

被引:94
作者
Weber, W
Rimann, M
Spielmann, M
Keller, B
Daoud-El Baba, M
Aubel, D
Weber, CC
Fussenegger, M
机构
[1] ETH Honggerberg, Swiss Fed Inst Technol, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[2] Inst Univ Technol, IUTA, Dept Genie Biol, F-69622 Villeurbanne, France
[3] ETH Zentrum, Swiss Fed Inst Technol, Inst Biomed Engn, CH-8044 Zurich, Switzerland
关键词
D O I
10.1038/nbt1021
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
We describe the design and detailed characterization of a gas-inducible transgene control system functional in different mammalian cells, mice and prototype biopharmaceutical manufacturing. The acetaldehyde-inducible AlcR-P-alcA transactivator-promoter interaction of the Aspergillus nidulans ethanol-catabolizing regulon(1) was engineered for gas-adjustable transgene expression in mammalian cells. Fungal AlcR retained its transactivation characteristics in a variety of mammalian cell lines and reversibly adjusted transgene transcription from chimeric mammalian promoters (P-AIR) containing P-alcA-derived operators in a gaseous acetaldehyde-dependent manner. Mice implanted with microencapsulated cells engineered for acetaldehyde-inducible regulation (AIR) of the human glycoprotein secreted placental alkaline phosphatase showed adjustable serum phosphatase levels after exposure to different gaseous acetaldehyde concentrations. AIR-controlled interferon-beta production in transgenic CHO-K1-derived serum-free suspension cultures could be modulated by fine-tuning inflow and outflow of acetaldehyde-containing gas during standard bioreactor operation. AIR technology could serve as a tool for therapeutic transgene dosing as well as biopharmaceutical manufacturing.
引用
收藏
页码:1440 / 1444
页数:5
相关论文
共 30 条
[1]   Design of a novel mammalian screening system for the detection of bioavailable, non-cytotoxic streptogramin antibiotics [J].
Aubel, D ;
Morris, R ;
Lennon, B ;
Rimann, M ;
Kaufmann, H ;
Folcher, M ;
Bailey, JE ;
Thompson, CJ ;
Fussenegger, M .
JOURNAL OF ANTIBIOTICS, 2001, 54 (01) :44-55
[2]   SECRETED PLACENTAL ALKALINE-PHOSPHATASE - A POWERFUL NEW QUANTITATIVE INDICATOR OF GENE-EXPRESSION IN EUKARYOTIC CELLS [J].
BERGER, J ;
HAUBER, J ;
HAUBER, R ;
GEIGER, R ;
CULLEN, BR .
GENE, 1988, 66 (01) :1-10
[3]   Long-term control of erythropoietin secretion by doxycycline in mice transplanted with engineered primary myoblasts [J].
Bohl, D ;
Naffakh, N ;
Heard, JM .
NATURE MEDICINE, 1997, 3 (03) :299-305
[4]   A temperature-regulated replicon-based DNA expression system [J].
Boorsma, M ;
Nieba, L ;
Koller, D ;
Bachmann, MF ;
Bailey, JE ;
Renner, WA .
NATURE BIOTECHNOLOGY, 2000, 18 (04) :429-432
[5]   NPAS2: A gas-responsive transcription factor [J].
Dioum, EM ;
Rutter, J ;
Tuckerman, JR ;
Gonzalez, G ;
Gilles-Gonzalez, MA ;
McKnight, SL .
SCIENCE, 2002, 298 (5602) :2385-2387
[6]   Lack of an immune response against the tetracycline-dependent transactivator correlates with long-term doxycycline-regulated transgene expression in nonhuman primates after intramuscular injection of recombinant adeno-associated virus [J].
Favre, D ;
Blouin, V ;
Provost, N ;
Spisek, R ;
Porrot, F ;
Bohl, D ;
Marmé, F ;
Chérel, Y ;
Salvetti, A ;
Hurtrel, B ;
Heard, JM ;
Rivière, Y ;
Moullier, P .
JOURNAL OF VIROLOGY, 2002, 76 (22) :11605-11611
[7]   THE ETHANOL REGULON IN ASPERGILLUS-NIDULANS - CHARACTERIZATION AND SEQUENCE OF THE POSITIVE REGULATORY GENE ALCR [J].
FELENBOK, B ;
SEQUEVAL, D ;
MATHIEU, M ;
SIBLEY, S ;
GWYNNE, DI ;
DAVIES, RW .
GENE, 1988, 73 (02) :385-396
[8]   Ethanol catabolism in Aspergillus nidulans:: A model system for studying gene regulation [J].
Felenbok, B ;
Flipphi, M ;
Nikolaev, I .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 69, 2001, 69 :149-204
[9]   Characteristics of physiological inducers of the ethanol utilization (alc) pathway in Aspergillus nidulans [J].
Flipphi, M ;
Kocialkowska, J ;
Felenbok, B .
BIOCHEMICAL JOURNAL, 2002, 364 :25-31
[10]   Streptogramin-based gene regulation systems for mammalian cells [J].
Fussenegger, M ;
Morris, RP ;
Fux, C ;
Rimann, M ;
von Stockar, B ;
Thompson, CJ ;
Bailey, JE .
NATURE BIOTECHNOLOGY, 2000, 18 (11) :1203-1208