Role of p53 in DNA strand break-induced apoptosis in organotypic slice culture from the mouse cerebellum

Apoptosis occurs not only in mitotic cells but also in postmitotic neuronal cells. We previously suggested that the tumor suppressor gene p53 is required for DNA strand break‐induced apoptosis in dissociated culture of cerebellar granule neurons. In this study, we examined the role of p53 in apoptos...

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Published inJournal of neuroscience research Vol. 60; no. 4; pp. 450 - 457
Main Authors Inamura, N., Araki, T., Enokido, Y., Nishio, C., Aizawa, S., Hatanaka, H.
Format Journal Article
LanguageEnglish
Published New York John Wiley & Sons, Inc 15.05.2000
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Abstract Apoptosis occurs not only in mitotic cells but also in postmitotic neuronal cells. We previously suggested that the tumor suppressor gene p53 is required for DNA strand break‐induced apoptosis in dissociated culture of cerebellar granule neurons. In this study, we examined the role of p53 in apoptosis using organotypic slice culture of cerebellum from p53 null and wild‐type mice. Exposure to bleomycin significantly increased the numbers of TUNEL‐, p53‐, and c‐Jun–positive neurons in the wild‐type mouse cerebellar internal granular layer (IGL) and Purkinje cell layer (PL). However, in p53‐deficient mice, these responses were not observed. These results are consistent with our previous observations in dissociated neuronal culture showing that the amount of c‐Jun protein increases significantly after addition of bleomycin in p53 wild‐type cerebellar granule cells. The results presented here also indicate that p53 is involved in DNA strand break‐induced apoptosis of fully postmitotic central nervous system neurons and suggest that c‐Jun expression occurs downstream of p53 expression. J. Neurosci. Res. 4:450–457, 2000 © 2000 Wiley‐Liss, Inc.
AbstractList Apoptosis occurs not only in mitotic cells but also in postmitotic neuronal cells. We previously suggested that the tumor suppressor gene p53 is required for DNA strand break-induced apoptosis in dissociated culture of cerebellar granule neurons. In this study, we examined the role of p53 in apoptosis using organotypic slice culture of cerebellum from p53 null and wild-type mice. Exposure to bleomycin significantly increased the numbers of TUNEL-, p53-, and c-Jun-positive neurons in the wild-type mouse cerebellar internal granular layer (IGL) and Purkinje cell layer (PL). However, in p53-deficient mice, these responses were not observed. These results are consistent with our previous observations in dissociated neuronal culture showing that the amount of c-Jun protein increases significantly after addition of bleomycin in p53 wild-type cerebellar granule cells. The results presented here also indicate that p53 is involved in DNA strand break-induced apoptosis of fully postmitotic central nervous system neurons and suggest that c-Jun expression occurs downstream of p53 expression.
Apoptosis occurs not only in mitotic cells but also in postmitotic neuronal cells. We previously suggested that the tumor suppressor gene p53 is required for DNA strand break‐induced apoptosis in dissociated culture of cerebellar granule neurons. In this study, we examined the role of p53 in apoptosis using organotypic slice culture of cerebellum from p53 null and wild‐type mice. Exposure to bleomycin significantly increased the numbers of TUNEL‐, p53‐, and c‐Jun–positive neurons in the wild‐type mouse cerebellar internal granular layer (IGL) and Purkinje cell layer (PL). However, in p53‐deficient mice, these responses were not observed. These results are consistent with our previous observations in dissociated neuronal culture showing that the amount of c‐Jun protein increases significantly after addition of bleomycin in p53 wild‐type cerebellar granule cells. The results presented here also indicate that p53 is involved in DNA strand break‐induced apoptosis of fully postmitotic central nervous system neurons and suggest that c‐Jun expression occurs downstream of p53 expression. J. Neurosci. Res. 4:450–457, 2000 © 2000 Wiley‐Liss, Inc.
Author Enokido, Y.
Araki, T.
Hatanaka, H.
Nishio, C.
Inamura, N.
Aizawa, S.
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Snippet Apoptosis occurs not only in mitotic cells but also in postmitotic neuronal cells. We previously suggested that the tumor suppressor gene p53 is required for...
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SubjectTerms Animals
Antibiotics, Antineoplastic - pharmacology
Apoptosis - physiology
Bleomycin - pharmacology
cell cycle
Cells, Cultured
Cerebellum - cytology
Cerebellum - drug effects
Cerebellum - metabolism
Chromosome Breakage
DNA repair
In Situ Nick-End Labeling
Mice
Mice, Knockout
Mice, Mutant Strains
neuronal cell death
Neurons - cytology
Neurons - drug effects
Neurons - metabolism
neurotrophin
programmed cell death
Proto-Oncogene Proteins c-fos - biosynthesis
Proto-Oncogene Proteins c-jun - biosynthesis
Purkinje Cells - cytology
Purkinje Cells - drug effects
Purkinje Cells - metabolism
Tumor Suppressor Protein p53 - genetics
Tumor Suppressor Protein p53 - metabolism
Title Role of p53 in DNA strand break-induced apoptosis in organotypic slice culture from the mouse cerebellum
URI https://api.istex.fr/ark:/67375/WNG-JVQVXFZ5-T/fulltext.pdf
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https://www.ncbi.nlm.nih.gov/pubmed/10797547
https://search.proquest.com/docview/17533305
https://search.proquest.com/docview/71096626
Volume 60
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