Development of a novel mouse glioma model using lentiviral vectors

被引:253
作者
Marumoto, Tomotoshi [1 ,2 ]
Tashiro, Ayumu [3 ,4 ]
Friedmann-Morvinski, Dinorah [1 ]
Scadeng, Miriam [5 ]
Soda, Yasushi [1 ]
Gage, Fred H. [1 ]
Verma, Inder M. [1 ]
机构
[1] Salk Inst Biol Studies, Genet Lab, La Jolla, CA 92037 USA
[2] Kobe Med Ctr Natl Hosp Org, Dept Neurosurg, Suma Ku, Kobe, Hyogo 6540155, Japan
[3] Memory Norwegian Univ Sci & Technol, Kavli Inst Syst Neurosci, Med Tech Res Ctr, NO-7489 Trondheim, Norway
[4] Memory Norwegian Univ Sci & Technol, Ctr Biol, Med Tech Res Ctr, NO-7489 Trondheim, Norway
[5] Univ Calif San Diego, Ctr Funct Magnet Resonance Imaging, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
HUMAN-BRAIN; GLIOBLASTOMA-MULTIFORME; GENETIC ALTERATIONS; TRANSGENIC MICE; EGF RECEPTOR; EXPRESSION; CELLS; IDENTIFICATION; PROLIFERATION; ASTROCYTES;
D O I
10.1038/nm.1863
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report the development of a new method to induce glioblastoma multiforme in adult immunocompetent mice by injecting Cre-loxP-controlled lentiviral vectors expressing oncogenes. Cell type- or region-specific expression of activated forms of the oncoproteins Harvey-Ras and AKT in fewer than 60 glial fibrillary acidic protein-positive cells in the hippocampus, subventricular zone or cortex of mice heterozygous for the gene encoding the tumor suppressor Tp53 were tested. Mice developed glioblastoma multiforme when transduced either in the subventricular zone or the hippocampus. However, tumors were rarely detected when the mice were transduced in the cortex. Transplantation of brain tumor cells into naive recipient mouse brain resulted in the formation of glioblastoma multiforme-like tumors, which contained CD133(+) cells, formed tumorspheres and could differentiate into neurons and astrocytes. We suggest that the use of Cre-loxP-controlled lentiviral vectors is a novel way to generate a mouse glioblastoma multiforme model in a region- and cell type-specific manner in adult mice.
引用
收藏
页码:110 / 116
页数:7
相关论文
共 35 条
[1]   STUDIES ON THE PROPERTIES OF P1 SITE-SPECIFIC RECOMBINATION - EVIDENCE FOR TOPOLOGICALLY UNLINKED PRODUCTS FOLLOWING RECOMBINATION [J].
ABREMSKI, K ;
HOESS, R ;
STERNBERG, N .
CELL, 1983, 32 (04) :1301-1311
[2]   MDM2 EXPRESSION IS INDUCED BY WILD TYPE-P53 ACTIVITY [J].
BARAK, Y ;
JUVEN, T ;
HAFFNER, R ;
OREN, M .
EMBO JOURNAL, 1993, 12 (02) :461-468
[3]  
DAHLSTRAND J, 1992, CANCER RES, V52, P5334
[4]   GFAP-expressing progenitors are the principal source of constitutive neurogenesis in adult mouse forebrain [J].
Denise, A ;
Garcia, R ;
Doan, NB ;
Imura, T ;
Bush, TG ;
Sofroniew, MV .
NATURE NEUROSCIENCE, 2004, 7 (11) :1233-1241
[5]   Subventricular zone astrocytes are neural stem cells in the adult mammalian brain [J].
Doetsch, F ;
Caillé, I ;
Lim, DA ;
García-Verdugo, JM ;
Alvarez-Buylla, A .
CELL, 1999, 97 (06) :703-716
[6]   A third-generation lentivirus vector with a conditional packaging system [J].
Dull, T ;
Zufferey, R ;
Kelly, M ;
Mandel, RJ ;
Nguyen, M ;
Trono, D ;
Naldini, L .
JOURNAL OF VIROLOGY, 1998, 72 (11) :8463-8471
[7]  
EKSTRAND AJ, 1994, ONCOGENE, V9, P2313
[8]  
FINKELSTEIN SD, 1994, NEUROSURGERY, V34, P136
[9]   SURVIVAL AND DIFFERENTIATION OF ADULT NEURONAL PROGENITOR CELLS TRANSPLANTED TO THE ADULT BRAIN [J].
GAGE, FH ;
COATES, PW ;
PALMER, TD ;
KUHN, HG ;
FISHER, LJ ;
SUHONEN, JO ;
PETERSON, DA ;
SUHR, ST ;
RAY, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (25) :11879-11883
[10]   Human-specific regulation of α2-6-linked sialic acids [J].
Gagneux, P ;
Cheriyan, M ;
Hurtado-Ziola, N ;
van der Linden, ECMB ;
Anderson, D ;
McClure, H ;
Varki, A ;
Varki, NM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (48) :48245-48250