ABSTRACT The voltage-gated potassium channel Kv1.2 is a key determinant of cellular excitability in the nervous and cardiovascular systems. In the brain, Kv1.2 is strongly expressed in neurons of the hippocampus, a structure essential for learning and memory, and the cerebellum, a structure essential for motor control and cognition. In the vasculature, Kv1.2 is expressed in smooth muscle cells where it contributes to the regulation of blood flow. Dynamic regulation of Kv1.2 is fundamental to its role in these tissues. Disruption of this regulation can manifest in a range of pathological conditions, including seizure, hypertension and neuropathic pain. Thus, elucidating the mechanisms by which Kv1.2 is regulated addresses fundamental aspects of human physiology and disease. Kv1.2 was the first voltage gated ion channel found to be regulated by tyrosine phosphorylation. The ionic current of Kv1.2 is suppressed following tyrosine phosphorylation by a process involving channel endocytosis. Movement of channel away from the plasma membrane involves many proteins associated with the cytoskeleton, including dynamin, cortactin and RhoA. Because trafficking of Kv1.2 away from the cell surface has emerged as the primary mechanism for its negative regulation, we hypothesized that trafficking of the channel to the cell surface could be a mechanism for positive regulation of the Kv1.2 ionic current. Activation of the cAMP/PKA pathway enhances the ionic current of Kv1.2. We hypothesized that a mechanism for this positive regulation is an increase in the amount of channel protein present at the cell surface. Our data show that cAMP can regulate Kv1.2 surface levels by two opposing trafficking pathways, one PKA-dependent and one PKA-independent. Channel homeostasis is preserved by the dynamic balance between these two pathways. Accordingly, any change in the levels of cAMP causes a net increase in the amount of Kv1.2 present at the cell surface. Specific C-terminal phosphorylation sites of Kv1.2 were identified and shown to have a role in maintaining basal surface channel levels. These findings demonstrate channel trafficking as a mechanism for the positive regulation of the Kv1.2 ionic current. In addition to Kv1.2 trafficking at the plasma membrane, movement of the channel from the biosynthetic pathway to the cell surface is another checkpoint for its regulation. Here we show that the protein arginine methyltransferase 8 (PRMT8) is able to promote the ER exit of Kv1.2, resulting in an increase in Kv1.2 surface expression. PRMT8 not only promoted surface expression of the high mannose glycosylated form of Kv1.2, characteristic of immature, ER-localized channels, but also enhanced Kv1.2 total protein levels, most likely by decreasing the amount of channel protein available for ER-associated degradation (ERAD). These findings highlight biosynthetic trafficking of Kv1.2 as a crucial part of its regulation and identify a novel role for PRMT8, as a regulator of biosynthetic protein trafficking.
| Identifer | oai:union.ndltd.org:uvm.edu/oai:scholarworks.uvm.edu:graddis-1051 |
| Date | 02 October 2009 |
| Creators | Connors, Emilee |
| Publisher | ScholarWorks @ UVM |
| Source Sets | University of Vermont |
| Detected Language | English |
| Type | text |
| Format | application/pdf |
| Source | Graduate College Dissertations and Theses |
Page generated in 0.0019 seconds