Adenovirus-mediated gene transfer of Bcl-xL prevents cell death in primary neuronal culture of the rat

被引:19
作者
Matsuoka, N
Yukawa, H
Ishii, K
Hamada, H
Akimoto, M
Hashimoto, N
Miyatake, S
机构
[1] Kyoto Univ, Fac Med, Dept Neurosurg & Clin Neurosci, Sakyo Ku, Kyoto 6068507, Japan
[2] Kyoto Univ, Inst Virus Res, Sakyo Ku, Kyoto 6068507, Japan
[3] Japanese Fdn Canc Res, Inst Canc, Ctr Canc Chemotherapy, Dept Mol Biotherapy Res,Toshima Ku, Tokyo 170, Japan
[4] Shinshu Univ, Dept Ophthalmol, Nagano 3900802, Japan
关键词
adenovirus; apoptosis; Bcl-xL; gene transfer; neuronal cell death; primary neuronal culture;
D O I
10.1016/S0304-3940(99)00499-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Bcl-xL is a Bcl-2-related gene that regulates programmed cell death in a bcl-2-independent fashion. It is expressed in tissues containing long-surviving postmitotic cells, such as neurons in adult brains. To investigate the possibility of gene therapy for transferring this anti-apoptotic gene into the neuron for the treatment of vascular occlusive or neurodegenerative diseases, we examined the effect of a replication-deficient recombinant adenovirus vector coding human Bcl-xL gene on the augmentation of the survival of primarily-cultured rat neuronal cells in vitro. Immunoblot analysis revealed that primarily-cultured neuronal cells were successfully infected and transferred with this gene by recombinant adenovirus vector with high transduction efficiency. Bcl-xL gene transfer to the primarily-cultured neurons could prevent these cells from cell death. (C) 1999 Elsevier Science Ireland ltd. All rights reserved.
引用
收藏
页码:177 / 180
页数:4
相关论文
共 15 条
[1]  
Akimoto M, 1999, INVEST OPHTH VIS SCI, V40, P273
[2]   CLONING THE CHROMOSOMAL BREAKPOINT OF T(14-18) HUMAN LYMPHOMAS - CLUSTERING AROUND JH ON CHROMOSOME-14 AND NEAR A TRANSCRIPTIONAL UNIT ON 18 [J].
BAKHSHI, A ;
JENSEN, JP ;
GOLDMAN, P ;
WRIGHT, JJ ;
MCBRIDE, OW ;
EPSTEIN, AL ;
KORSMEYER, SJ .
CELL, 1985, 41 (03) :899-906
[3]   BCL-X, A BCL-2-RELATED GENE THAT FUNCTIONS AS A DOMINANT REGULATOR OF APOPTOTIC CELL-DEATH [J].
BOISE, LH ;
GONZALEZGARCIA, M ;
POSTEMA, CE ;
DING, LY ;
LINDSTEN, T ;
TURKA, LA ;
MAO, XH ;
NUNEZ, G ;
THOMPSON, CB .
CELL, 1993, 74 (04) :597-608
[4]   APOPTOSIS - FINAL COMMON PATHWAY OF PHOTORECEPTOR DEATH IN RD, RDS, AND RHODOPSIN MUTANT MICE [J].
CHANG, GQ ;
HAO, Y ;
WONG, F .
NEURON, 1993, 11 (04) :595-605
[5]   INDUCTION OF APOPTOSIS BY THE BCL-2 HOMOLOG BAK [J].
CHITTENDEN, T ;
HARRINGTON, EA ;
OCONNOR, R ;
FLEMINGTON, C ;
LUTZ, RJ ;
EVAN, GI ;
GUILD, BC .
NATURE, 1995, 374 (6524) :733-736
[6]   C-ELEGANS CELL-SURVIVAL GENE CED-9 ENCODES A FUNCTIONAL HOMOLOG OF THE MAMMALIAN PROTOONCOGENE BCL-2 [J].
HENGARTNER, MO ;
HORVITZ, HR .
CELL, 1994, 76 (04) :665-676
[7]   EFFECTS OF 2-MERCAPTOETHANOL ON SURVIVAL AND DIFFERENTIATION OF FETAL MOUSE-BRAIN NEURONS CULTURED IN-VITRO [J].
ISHII, K ;
KATAYAMA, M ;
HORI, K ;
YODOI, J ;
NAKANISHI, T .
NEUROSCIENCE LETTERS, 1993, 163 (02) :159-162
[8]   BCL-2 INHIBITION OF NEURAL DEATH - DECREASED GENERATION OF REACTIVE OXYGEN SPECIES [J].
KANE, DJ ;
SARAFIAN, TA ;
ANTON, R ;
HAHN, H ;
GRALLA, EB ;
VALENTINE, JS ;
ORD, T ;
BREDESEN, DE .
SCIENCE, 1993, 262 (5137) :1274-1277
[9]   Efficient gene activation system on mammalian cell chromosomes using recombinant adenovirus producing Cre recombinase [J].
Kanegae, Y ;
Takamori, K ;
Sato, Y ;
Lee, G ;
Nakai, M ;
Saito, I .
GENE, 1996, 181 (1-2) :207-212
[10]   2-MERCAPTOETHANOL-INDEPENDENT SURVIVAL OF FETAL MOUSE-BRAIN NEURONS CULTURED IN A MEDIUM OF HUMAN SERUM [J].
KATAYAMA, M ;
ISHII, K .
BRAIN RESEARCH, 1994, 656 (02) :409-412