Rapid regulation of dopamine transporters by tyrosine kinases in rat neuronal preparations
Article first published online: 26 FEB 2007
Journal of Neurochemistry
Volume 101, Issue 5, pages 1258–1271, June 2007
How to Cite
Hoover, B. R., Everett, C. V., Sorkin, A. and Zahniser, N. R. (2007), Rapid regulation of dopamine transporters by tyrosine kinases in rat neuronal preparations. Journal of Neurochemistry, 101: 1258–1271. doi: 10.1111/j.1471-4159.2007.04522.x
- Issue published online: 26 FEB 2007
- Article first published online: 26 FEB 2007
- Received August 23, 2006; revised manuscript received November 30, 2006; accepted December 1, 2006.
- brain-derived neurotrophic factor;
- dopamine transporter;
- dopamine uptake;
- tyrosine kinases
Termination of dopamine neurotransmission is primarily controlled by the plasma membrane-localized dopamine transporter. In this study, we investigated how this transporter is regulated by tyrosine kinases in neuronal preparations. In rat dorsal striatal synaptosomes, inhibition of tyrosine kinases by genistein or tyrphostin 23 resulted in a rapid (5–15 min), concentration-dependent decrease in [3H]dopamine uptake because of a reduction in maximal [3H]dopamine uptake velocity and dopamine transporter cell surface expression. The reduced transporter activity was associated with a decrease in phosphorylated p44/p42 mitogen-activated protein kinases. In primary rat mesencephalic neuronal cultures, the tyrosine kinase inhibitors similarly reduced [3H]dopamine uptake. When cultures were serum-deprived, acute activation of tyrosine kinase-coupled TrkB receptors by 100 ng/mL brain-derived neurotrophic factor significantly increased [3H]dopamine uptake; the effects were complex with increased maximal velocity but reduced affinity. The facilitatory effect of brain-derived neurotrophic factor on dopamine transporter activity depended on both the mitogen-activated protein kinase and phosphatidylinositol 3-kinase pathways. Taken together, our results suggest that striatal dopamine transporter function and cell surface expression is constitutively up-regulated by tyrosine kinase activation and that brain-derived neurotrophic factor can mediate this type of rapid regulation.