Abstract
Nerve growth factor is a neurotrophic factor that regulates neuronal cell development, maintenance, and injury responses in the peripheral and central nervous system. Nerve growth factor reduces injury owing to oxidative stress in rat pheochromocytoma (PC12) cells by increasing intracellular glutathione, in part owing to its stimulation of the activity of γ-glutamylcysteine synthetase, which is the rate-limiting enzyme in the synthesis of glutathione. Here we show that nerve growth factor did not increase the activity of γ-glutamylcysteine synthetase in PC12 cells at the transcriptional level. Rather, nerve growth factor enhanced the stability of γ-glutamylcysteine synthetase mRNA in PC12 cells. These results suggest that, during oxidative stress, nerve growth factor extended the half-life of γ-glutamylcysteine synthetase mRNA, thus increasing γ-glutamylcysteine synthetase mRNA levels compared to nerve growth factor-deprived PC12 cells.
Original language | English (US) |
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Pages (from-to) | 559-566 |
Number of pages | 8 |
Journal | International Journal of Developmental Neuroscience |
Volume | 14 |
Issue number | 5 |
DOIs | |
State | Published - Aug 1996 |
Keywords
- Glutathione
- Nerve growth factor
- PC12
- γ-glutamylcysteine synthetase
ASJC Scopus subject areas
- Developmental Neuroscience
- Developmental Biology