Cited by 107Cell death mechanisms and regulationNeurogenesis and neuroplasticity mechanismsDevelopmental Biology and Gene Regulation

The proapoptotic activities of Bax and Bak limit the size of the neural stem cell pool

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Lindsten, Tullia, Golden, Jeffrey A., Zong, Wei-Xing, Minarcik, Jeremy, Harris, Marian H., Thompson, Craig B.·2003·The Journal of Neuroscience

Abstract

The proapoptotic Bcl-2 family members Bak and Bax play central and redundant roles in the regulation of apoptosis. In this study, we investigated the effect of loss of Bax and Bak in the CNS. The adult bax-/-bak-/- mice display masses of densely staining cells in the proliferative zones of the brain. These cells are shown to be a mix of neural progenitor cells and postmitotic cells at different stages of neural and glial differentiation. Both neural progenitor cells and mature neurons derived from bax-/-bak-/- mice were resistant to various apoptotic stimuli. Despite this resistance, postmitotic mature bax-/-bak-/- neurons remain as sensitive to excitoxic death as wild-type neurons. Thus, Bax and Bak play a critical role in regulating the number of neural progenitor cells in the adult brain but are not absolutely required for the initiation of neuronal cell death after neurotoxic injury.

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Crossref · 10.1523/jneurosci.23-35-11112.2003

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  • Growth factor-deprived hematopoietic and neuronal cells fail to consume glucose in quantities sufficient to maintain cellular bioenergetics.

    “when deprived of growth factors, hematopoietic and neuronal cells fail to consume glucose in quantities sufficient to even maintain cellular bioenergetics”

    From The emerging hallmarks of cancer metabolism (2016) · cites this paper as Lindsten et al., 2003

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Authors
Lindsten, T., Golden, J. A., Zong, W.-X., Minarcik, J., Harris, M. H., & Thompson, C. B.
Affiliations
Children's Hospital of Philadelphia (US)
Venue
The Journal of Neuroscience
Published
2003-12-03
Volume
23
Issue
35
Pages
11112-11119
ISSN
  • 0270-6474 (ISSN-L)
  • 1529-2401
OpenAlex
W1953301620
Cited by
107
References
27
Citations by year
2025: 1 · 2024: 3 · 2022: 1 · 2021: 3 · 2020: 2 · 2019: 2 · 2017: 3 · 2016: 7 · 2015: 5 · 2014: 2 · 2013: 3 · 2012: 10
FWCI
3.10
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Cancer Research Institute
  • National Institutes of Health (HD 26979)
  • Directorate for Biological Sciences
  • National Cancer Institute
  • National Institute of Child Health and Human Development (HD26979)
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (P30HD026979, HD 26979)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
Keywords
Bax, Bak, Bcl-2 family proteins, apoptosis, neural stem cells, neural progenitor cells, excitotoxicity, neuronal cell death, glial differentiation, brain development
MeSH terms
Animals, Antigens, Differentiation, Cell Count, Cell Division, Cells, Cultured, Cerebellum, Flow Cytometry, Membrane Proteins, Neurons, Proto-Oncogene Proteins, Stem Cells, Apoptosis, Mice, Knockout, Proto-Oncogene Proteins c-bcl-2, Lateral Ventricles, bcl-2 Homologous Antagonist-Killer Protein, bcl-2-Associated X Protein, Mice

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