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Basic Fibroblast Growth Factor in the Adrenal Gland
Dieter Blottner1, Reiner Westermann, Claudia Grothe
1Department of Anatomy and Cell Biology, University of Marburg, D-3550 Marburg, FRG.
The European Journal of Neuroscience
|September 1, 1989
Summary
Basic fibroblast growth factor (bFGF) in adrenal medulla supports spinal cord neurons. This suggests bFGF acts as a retrograde trophic messenger, maintaining neuron survival and function.
Area of Science:
- Neuroscience
- Cell Biology
Background:
- Trophic factors are crucial for neuronal development and maintenance.
- Nerve growth factor (NGF) exemplifies trophic support from target organs to neurons.
- The concept of target organ-regulated neuronal maintenance implies retrograde trophic support.
Purpose of the Study:
- To investigate the role of basic fibroblast growth factor (bFGF) in retrograde trophic neuron-neuron interaction.
- To determine if bFGF is present in the adrenal medulla and supports autonomic spinal cord neurons.
Main Methods:
- Western blotting and immunostaining to detect bFGF in adrenal medulla extracts and chromaffin cells.
- Assessing the effect of a bFGF-specific antibody on adrenal medullary extract activity.
- Evaluating the mitogenic activity of chromaffin granule proteins on endothelial cells.
- Investigating the impact of adrenal medulla destruction and bFGF substitution on spinal cord neurons.
Main Results:
- Basic fibroblast growth factor (bFGF) or a related protein is present in the adrenal medulla and chromaffin cells.
- Antibodies against bFGF blocked trophic activity in adrenal medullary extracts, supporting neuron survival in vitro.
- Soluble proteins from chromaffin granules exhibited mitogenic activity on endothelial cells.
- Destruction of the adrenal medulla led to significant loss of spinal cord neurons, which was prevented by bFGF substitution.
Conclusions:
- Basic fibroblast growth factor (bFGF) is localized in chromaffin cells.
- bFGF maintains target-deprived autonomic spinal cord neurons, acting as an interneuronal trophic messenger in vivo.