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Vol. 287, Issue 2, 744-751, November 1998
Department of Pharmacology and Center for Molecular Neuroscience,
Vanderbilt University School of Medicine, Nashville, Tennessee
Norepinephrine (NE) transporters (NETs) found in the neuronal plasma
membrane mediate the removal of NE from the extracellular space,
limiting the activation of adrenoceptors at noradrenergic synapses. Our
previous studies with the noradrenergic neuroblastoma SK-N-SH have
revealed a muscarinic receptor-triggered regulation of NET surface
density and transport capacity, mediated in part by protein kinase C
activation. Low abundance of NET proteins in this native cell model,
however, preclude direct confirmation of altered trafficking of NET
proteins. In our study, we monitored the activity and surface
distribution of human NET proteins in transient and stably-transfected
cell lines after application of kinase activators and inhibitors. Using
hNET stably transfected HEK-293 and LLC-PK1 cells, as well as
transiently transfected COS-7 cells, we demonstrate that PKC-activating
phorbol esters,
-PMA or
-PDBu selectively diminish l-NE transport
capacity (Vmax) with little change in NE Km.
Effects of phorbol esters are rapid, stereospecific and blocked by
protein kinase C inhibitors, staurosporine and bisindolylmaleimide I. As in SK-N-SH cells,
-PMA induces a reduction in intact cell
[3H]nisoxetine binding sites with no change in nisoxetine
Kd or total membrane NET density. Cell-surface
biotinylation and confocal immunofluorescence techniques confirm that
protein kinase C-dependent reductions in NE transport capacity and
whole-cell antagonist binding density are accompanied by reductions in
cell-surface human NET protein expression. Together these findings
argue for kinase-modulated protein trafficking as a potential route for acute regulation of antidepressant-sensitive NE clearance.
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