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 in | Journal of neuroscience research Vol. 60; no. 4; pp. 450 - 457 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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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. |
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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. |
Author_xml | – sequence: 1 givenname: N. surname: Inamura fullname: Inamura, N. organization: Division of Protein Biosynthesis, Institute for Protein Research, Osaka University, Osaka, Japan – sequence: 2 givenname: T. surname: Araki fullname: Araki, T. organization: Division of Protein Biosynthesis, Institute for Protein Research, Osaka University, Osaka, Japan – sequence: 3 givenname: Y. surname: Enokido fullname: Enokido, Y. organization: Division of Protein Biosynthesis, Institute for Protein Research, Osaka University, Osaka, Japan – sequence: 4 givenname: C. surname: Nishio fullname: Nishio, C. organization: Division of Protein Biosynthesis, Institute for Protein Research, Osaka University, Osaka, Japan – sequence: 5 givenname: S. surname: Aizawa fullname: Aizawa, S. organization: Department of Morphogenesis, Institute of Molecular Embryology and Genetics, Kumamoto University School of Medicine, Kumamoto, Japan – sequence: 6 givenname: H. surname: Hatanaka fullname: Hatanaka, H. email: hatanaka@protein.osaka-u.ac.jp organization: Division of Protein Biosynthesis, Institute for Protein Research, Osaka University, Osaka, Japan |
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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 |
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