Differences in survival-promoting effects and intracellular signaling properties of BDNF and IGF-1 in cultured cerebral cortical neurons
Autor: | Hiroshi Hatanaka, Toshihiko Ikeuchi, Keiko Tanabe, Yasuyuki Ishikawa, Koji Shimoke, Kazuyo Wada, Masashi Yamada, Shinichi Koizumi |
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Rok vydání: | 2001 |
Předmět: |
MAPK/ERK pathway
Brain-derived neurotrophic factor medicine.medical_specialty Biology CREB Biochemistry Cellular and Molecular Neuroscience Endocrinology nervous system Neurotrophic factors Internal medicine medicine biology.protein Phosphorylation Signal transduction Protein kinase A Protein kinase B |
Zdroj: | Journal of Neurochemistry. 78:940-951 |
ISSN: | 0022-3042 |
DOI: | 10.1046/j.1471-4159.2001.00497.x |
Popis: | Brain-derived neurotrophic factor (BDNF) and insulin-like growth factor-1 (IGF-1) act on various neurons of the CNS as neurotrophic factors promoting neuronal differentiation and survival. We examined the survival-promoting effects of BDNF and IGF-1 on serum deprivation-induced death in cultured cerebral cortical neurons, and compared the intracellular signaling pathways stimulated by BDNF and IGF-1 in the neurons. We found that the survival-promoting effect of BDNF was much weaker than that of IGF-1 in serum deprivation-induced death of cultured cortical neurons. We found no differences in the levels of phosphatidylinositol 3-kinase (PtdIns3-K) activity or Akt (also called PKB) phosphorylation induced by BDNF and IGF-1 in the cultured cortical neurons, although many reports suggest that PtdIns3-K and Akt are involved in survival promotion. In addition, phosphorylation signals of mitogen-activated protein kinase (MAPK) and cAMP responsive element-binding protein (CREB), which have also been reported to be involved in survival promotion, were stimulated by BDNF much more potently than by IGF-1. These results show that there may be, as yet unidentified, intracellular signaling pathways other than the PtdIns3-K-Akt, MAPK and CREB signaling, to regulate survival promotion. These unidentified signaling pathways may be responsible for the distinct strengths of the survival-promoting effects of BDNF and IGF-1. |
Databáze: | OpenAIRE |
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