Key result
Kv2.1 exhibits robust clustering and enhanced phosphorylation in M phase versus interphase cells, resulting in enhanced plasma membrane-endoplasmic reticulum membrane contact sites.
Cell cycle-dependent regulation of Kv2.1 localization and phosphorylation impacts plasma membrane-endoplasmic reticulum membrane contact sites during mitosis.
Background: Kv2.1 channels are components of plasma membrane:endoplasmic reticulum membrane contact sites (PM:ER MCS). Results: Kv2.1 exhibits clustering and enhanced phosphorylation in M phase versus interphase COS-1 cells, resulting in enhanced PM:ER MCS. Conclusion: Cell cycle-dependent regulation of Kv2.1 localization and phosphorylation impacts PM:ER MCS. Significance: PM:ER MCS are regulated by changes in PM protein localization and phosphorylation during mitosis. The plasma membrane (PM) comprises distinct subcellular domains with diverse functions that need to be dynamically coordinated with intracellular events, one of the most impactful being mitosis. The Kv2.1 voltage-gated potassium channel is conditionally localized to large PM clusters that represent specialized PM:endoplasmic reticulum membrane contact sites (PM:ER MCS), and overexpression of Kv2.1 induces more exuberant PM:ER MCS in neurons and in certain heterologous cell types. Localization of Kv2.1 at these contact sites is dynamically regulated by changes in phosphorylation at one or more sites located on its large cytoplasmic C terminus. Here, we show that Kv2.1 expressed in COS-1 cells undergoes dramatic cell cycledependent changes in its PM localization, having diffuse localization in interphase cells, and robust clustering during M phase. The mitosis-specific clusters of Kv2.1 are localized to PM:ER MCS, and M phase clustering of Kv2.1 induces more extensive PM:ER MCS. These cell cycle-dependent changes in Kv2.1 localization and the induction of PM:ER MCS are accompanied by increased mitotic Kv2.1 phosphorylation at several C-terminal phosphorylation sites. Phosphorylation of exogenously expressed Kv2.1 is significantly increased upon metaphase arrest in COS-1 and CHO cells, and in a pancreatic cell line that express endogenous Kv2.1. The M phase clustering of Kv2.1 at PM:ER MCS in COS-1 cells requires the same C-terminal targeting motif needed for conditional Kv2.1 clustering in neurons. The cell cycle-dependent changes in localization and phosphorylation of Kv2.1 were not accompanied by changes in the electrophysiological properties of Kv2.1 expressed in CHO cells. Together, these results provide novel insights into the cell cycle-dependent changes in PM protein localization and phosphorylation.
No takes yet. Share an insight, caveat, or question.
Cobb et al. (2015) studied Cell cycle-dependent regulation of Kv2.1. Kv2.1 expression vs. Interphase cells was evaluated on Kv2.1 localization and phosphorylation. Kv2.1 exhibits robust clustering and enhanced phosphorylation in M phase versus interphase cells, resulting in enhanced plasma membrane-endoplasmic reticulum membrane contact sites.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: