Hippocampal neurons of mice deficient in DNA-dependent protein kinase exhibit increased vulnerability to DNA damage, oxidative stress and excitotoxicity
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作者:
Culmsee, C
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机构:NIA, Gerontol Res Ctr, Neurosci Lab, Baltimore, MD 21224 USA
Culmsee, C
Bondada, S
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机构:NIA, Gerontol Res Ctr, Neurosci Lab, Baltimore, MD 21224 USA
Bondada, S
Mattson, MP
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机构:NIA, Gerontol Res Ctr, Neurosci Lab, Baltimore, MD 21224 USA
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
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.