Hippocampal neurons of mice deficient in DNA-dependent protein kinase exhibit increased vulnerability to DNA damage, oxidative stress and excitotoxicity

被引:66
作者
Culmsee, C
Bondada, S
Mattson, MP
机构
[1] NIA, Gerontol Res Ctr, Neurosci Lab, Baltimore, MD 21224 USA
[2] Univ Kentucky, Sanders Brown Ctr Aging, Lexington, KY 40536 USA
[3] Univ Marburg, Inst Pharmakol & Toxikol, D-35037 Marburg, Germany
[4] Univ Kentucky, Dept Microbiol & Immunol, Lexington, KY 40536 USA
[5] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
来源
MOLECULAR BRAIN RESEARCH | 2001年 / 87卷 / 02期
关键词
Alzheimer's disease; amyloid beta-peptide; DNA repair; epileptic seizure; glutamate; topoisomerase inhibitor;
D O I
10.1016/S0169-328X(01)00008-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
DNA damage has been documented in neurodegenerative conditions ranging from Alzheimer's disease to stroke. DNA-dependent protein kinase (DNA-PK) is involved in V(D)J recombination and DNA double strand break repair, and may play a role in cell death induced by DNA damage. We now report that cultured hippocampal neurons from severe combined immunodeficient (scid) mice which lack DNA-PK activity are hypersensitive to apoptosis induced by exposure to topoisomerase inhibitors, amyloid beta peptide (AP) and glutamate. A similar increased vulnerability of hippocampal CAI and CA3 neurons was observed in adult scid mice after kainate-induced seizures. Our results suggest that DNA-PK activity is important for neuron survival under conditions that may occur in neurological disorders. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:257 / 262
页数:6
相关论文
共 48 条
[21]   DNA-dependent protein kinase is not required for the p53-dependent response to DNA damage [J].
Jimenez, GS ;
Bryntesson, F ;
Torres-Arzayus, MI ;
Priestley, A ;
Beeche, M ;
Saito, S ;
Sakaguchi, K ;
Appella, E ;
Jeggo, PA ;
Taccioli, GE ;
Wahl, GM ;
Hubank, M .
NATURE, 1999, 400 (6739) :81-83
[22]   The ability of p53 to activate downstream genes p21WAF1/cip1 and MDM2, and cell cycle arrest following DNA damage is delayed and attenuated in scid cells deficient in the DNA-dependent protein [J].
Kachnic, LA ;
Wu, B ;
Wunsch, H ;
Mekeel, KL ;
DeFrank, JS ;
Tang, W ;
Powell, SN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (19) :13111-13117
[23]   DNA-DEPENDENT KINASE (P350) AS A CANDIDATE GENE FOR THE MURINE SCID DEFECT [J].
KIRCHGESSNER, CU ;
PATIL, CK ;
EVANS, JW ;
CUOMO, CA ;
FRIED, LM ;
CARTER, T ;
OETTINGER, MA ;
BROWN, JM .
SCIENCE, 1995, 267 (5201) :1178-1183
[24]  
Kruman I, 1997, J NEUROSCI, V17, P5089
[25]   Homocysteine elicits a DNA damage response in neurons that promotes apoptosis and hypersensitivity to excitotoxicity [J].
Kruman, II ;
Culmsee, C ;
Chan, SL ;
Kruman, Y ;
Guo, ZH ;
Penix, L ;
Mattson, MP .
JOURNAL OF NEUROSCIENCE, 2000, 20 (18) :6920-6926
[26]   The DNA-dependent protein kinase, DNA-PK: 10 years and no ends in sight [J].
LeesMiller, SP .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1996, 74 (04) :503-512
[27]   Tying loose ends: Roles of Ku and DNA-dependent protein kinase in the repair of double-strand breaks [J].
Lieber, MR ;
Grawunder, U ;
Wu, XT ;
Yaneva, M .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1997, 7 (01) :99-104
[28]   Ischemic cell death in brain neurons [J].
Lipton, P .
PHYSIOLOGICAL REVIEWS, 1999, 79 (04) :1431-1568
[29]  
Liu PK, 1996, J NEUROSCI, V16, P6795
[30]   Apoptosis and expression of DNA repair proteins in ischaemic brain injury in man [J].
Love, S ;
Barber, R ;
Wilcock, GK .
NEUROREPORT, 1998, 9 (06) :955-959