DNA damage-induced cell death: lessons from the central nervous system

DNA damage can, but does not always, induce cell death. While several pathways linking DNA damage signals to mitochondria-dependent and -independent death machineries have been elucidated, the connectivity of these pathways is subject to regulation by multiple other factors that are not well underst...

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Published in:Cell research Vol. 18; no. 1; pp. 17 - 26
Main Authors: Borges, Helena Lobo, Linden, Rafael, Wang, Jean YJ
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 01.01.2008
Nature Publishing Group
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ISSN:1001-0602, 1748-7838, 1748-7838
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Abstract DNA damage can, but does not always, induce cell death. While several pathways linking DNA damage signals to mitochondria-dependent and -independent death machineries have been elucidated, the connectivity of these pathways is subject to regulation by multiple other factors that are not well understood. We have proposed two conceptual models to explain the delayed and variable cell death response to DNA damage: integrative surveillance versus autonomous pathways. In this review, we discuss how these two models may explain the in vivo regulation of cell death induced by ionizing radiation (IR) in the developing central nervous system, where the death response is regulated by radiation dose, cell cycle status and neuronal development.
AbstractList DNA damage can, but does not always, induce cell death. While several pathways linking DNA damage signals to mitochondria-dependent and -independent death machineries have been elucidated, the connectivity of these pathways is subject to regulation by multiple other factors that are not well understood. We have proposed two conceptual models to explain the delayed and variable cell death response to DNA damage: integrative surveillance versus autonomous pathways. In this review, we discuss how these two models may explain the in vivo regulation of cell death induced by ionizing radiation (IR) in the developing central nervous system, where the death response is regulated by radiation dose, cell cycle status and neuronal development.
DNA damage can, but does not always, induce cell death. While several pathways linking DNA damage signals to mitochondria-dependent and -independent death machineries have been elucidated, the connectivity of these pathways is subject to regulation by multiple other factors that are not well understood. We have proposed two conceptual models to explain the delayed and variable cell death response to DNA damage: integrative surveillance versus autonomous pathways. In this review, we discuss how these two models may explain the in vivo regulation of cell death induced by ionizing radiation (IR) in the developing central nervous system, where the death response is regulated by radiation dose, cell cycle status and neuronal development.
DNA damage can, but does not always, induce cell death. While several pathways linking DNA damage signals to mitochondria-dependent and -independent death machineries have been elucidated, the connectivity of these pathways is subject to regulation by multiple other factors that are not well understood. We have proposed two conceptual models to explain the delayed and variable cell death response to DNA damage: integrative surveillance versus autonomous pathways . In this review, we discuss how these two models may explain the in vivo regulation of cell death induced by ionizing radiation (IR) in the developing central nervous system, where the death response is regulated by radiation dose, cell cycle status and neuronal development.
DNA damage can, but does not always, induce cell death. While several pathways linking DNA damage signals to mitochondria-dependent and -independent death machineries have been elucidated, the connectivity of these pathways is subject to regulation by multiple other factors that are not well understood. We have proposed two conceptual models to explain the delayed and variable cell death response to DNA damage: integrative surveillance versus autonomous pathways. In this review, we discuss how these two models may explain the in vivo regulation of cell death induced by ionizing radiation (IR) in the developing central nervous system, where the death response is regulated by radiation dose, cell cycle status and neuronal development.DNA damage can, but does not always, induce cell death. While several pathways linking DNA damage signals to mitochondria-dependent and -independent death machineries have been elucidated, the connectivity of these pathways is subject to regulation by multiple other factors that are not well understood. We have proposed two conceptual models to explain the delayed and variable cell death response to DNA damage: integrative surveillance versus autonomous pathways. In this review, we discuss how these two models may explain the in vivo regulation of cell death induced by ionizing radiation (IR) in the developing central nervous system, where the death response is regulated by radiation dose, cell cycle status and neuronal development.
Author Helena Lobo Borges Rafael Linden Jean YJ Wang
AuthorAffiliation Division of Hematology/Oncology, Moores Cancer Center, Department of Medicine, University of California, San Diego, 3855 Health Sciences, La Jolla, CA 92093-0820, USA; Departamento de Anatomia, Instituto de Ciencias Biomedicas, Universidade Federal do Rio de Janeiro, Centro de Ciencias da Saude, Cidade Universitaria, 21940-590 Rio de Janeiro, Brazil; Instiuto de Biofisica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Centro de Ciencias da Saude, Cidade Universiteria, 21940-590 Rio de Janeiro, Brazil
AuthorAffiliation_xml – name: 3 Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Centro de Ciências da Saúde, Cidade Universitária, 21940-590 Rio de Janeiro, Brazil
– name: 2 Departamento de Anatomia, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Centro de Ciências da Saúde, Cidade Universitária, 21940-590 Rio de Janeiro, Brazil
– name: 1 Division of Hematology/Oncology, Moores Cancer Center, Department of Medicine, University of California, San Diego, 3855 Health Sciences, La Jolla, CA 92093-0820, USA
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  givenname: Helena Lobo
  surname: Borges
  fullname: Borges, Helena Lobo
  organization: Division of Hematology/Oncology, Department of Medicine, Moores Cancer Center, University of California, San Diego, Departamento de Anatomia, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Centro de Ciências da Saúde, Cidade Universitária
– sequence: 2
  givenname: Rafael
  surname: Linden
  fullname: Linden, Rafael
  organization: Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Centro de Ciências da Saúde, Cidade Universitária
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  givenname: Jean YJ
  surname: Wang
  fullname: Wang, Jean YJ
  email: jywang@ucsd.edu
  organization: Division of Hematology/Oncology, Department of Medicine, Moores Cancer Center, University of California, San Diego
BackLink https://www.ncbi.nlm.nih.gov/pubmed/18087290$$D View this record in MEDLINE/PubMed
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DocumentTitleAlternate DNA damage-induced cell death: lessons from the central nervous system
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Issue 1
Keywords apoptosis
neonatal retina
ATM
phosphorylation
ionizing radiation
neuroblasts
p53
Language English
License http://www.springer.com/tdm
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apoptosis, ATM, ionizing radiation, neonatal retina, neuroblasts, p53, phosphorylation
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Snippet DNA damage can, but does not always, induce cell death. While several pathways linking DNA damage signals to mitochondria-dependent and -independent death...
DNA damage can, but does not always, induce cell death. While several pathways linking DNA damage signals to mitochondria-dependent and - independent death...
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StartPage 17
SubjectTerms Animals
Apoptosis - genetics
Apoptosis - radiation effects
Biomedical and Life Sciences
Caspases - metabolism
Caspases - physiology
Cell Biology
Cell death
Cell Death - genetics
Cell Death - radiation effects
Central nervous system
Deoxyribonucleic acid
DNA
DNA Damage - physiology
DNA Fragmentation
Enzyme Activation - physiology
Enzyme Activation - radiation effects
Humans
Ionizing radiation
Life Sciences
Models, Biological
Mortality
Radiation Dosage
Radiation Injuries, Experimental - genetics
Radiation, Ionizing
Retina - growth & development
Retina - radiation effects
review
死亡过程
神经系统
脱氧核糖核酸
Title DNA damage-induced cell death: lessons from the central nervous system
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https://pubmed.ncbi.nlm.nih.gov/PMC2626635
Volume 18
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