Protein tyrosine kinase inhibitors synergize with nerve growth factor in embryonic chick sensory neuronal cell survival
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1Developmental Neurobiology, Division of Neuroscience, The John Curtin School of Medical Research, Australian National University, Canberra, ACT. selena.bartlett@anu.edu.au
Abstract:
The survival of developing sensory neurons is dependent upon target-derived growth factors, in their absence neurons undergo programmed cell death. The molecular mechanisms underpinning neuronal cell survival and death are poorly understood. Tyrosine kinases are important signalling proteins that have been implicated in both cell survival and death. The aim of this study was to examine the effects of tyrosine kinase inhibition on embryonic chick sensory neuronal survival using the tyrosine kinase inhibitors, herbimycin, genistein and tyrphostin. In low concentrations of nerve growth factor, NGF (100 fg/ml), the majority of neurons die, however neuronal survival was significantly potentiated in the presence of each of the tyrosine kinase inhibitors, herbimycin (40 ng/ml), genistein (2.5 microM) and tyrphostin (8 microM). In the presence of each of these inhibitors, sensory neurons exhibited typical phase bright morphology and fibre outgrowth was increased. These results demonstrate that the tyrosine kinase inhibitors support the survival of neurons in the presence of low concentrations of NGF. Herbimycin was used at lower concentrations than previously reported, and at this concentration it has been shown to be noncytotoxic in animals. Therefore it will be important to determine if herbimycin can be used as a therapeutic agent for enhancing nerve regeneration following injury.
Insights
Tyrosine kinase inhibitors promote the survival of developing sensory neurons when nerve growth factor (NGF) is limited. This finding suggests potential therapeutic applications for nerve regeneration and repair.
Area of Science:
- Neuroscience
- Molecular Biology
- Cell Biology
Background:
- Developing sensory neuron survival relies on target-derived growth factors.
- Insufficient growth factors trigger programmed cell death in neurons.
- Molecular mechanisms of neuronal survival and death are not fully understood.
Purpose of the Study:
- To investigate the impact of tyrosine kinase inhibitors on embryonic chick sensory neuron survival.
- To assess the effects of herbimycin, genistein, and tyrphostin on neuronal survival.
Main Methods:
- Utilized tyrosine kinase inhibitors: herbimycin, genistein, and tyrphostin.
- Cultured embryonic chick sensory neurons under low nerve growth factor (NGF) conditions.
- Quantified neuronal survival and observed morphology and fiber outgrowth.
Main Results:
- Tyrosine kinase inhibitors significantly enhanced sensory neuron survival in low NGF concentrations.
- Neurons treated with inhibitors displayed improved morphology and increased fiber outgrowth.
- Herbimycin demonstrated efficacy at a non-cytotoxic concentration.
Conclusions:
- Tyrosine kinase inhibitors support sensory neuron survival under conditions of limited NGF.
- Herbimycin shows promise as a potential therapeutic agent for nerve regeneration.
- Further research is warranted to explore herbimycin's therapeutic potential for nerve injury recovery.