Publication | Open Access
CaMKII-Dependent Phosphorylation of the GTPase Rem2 Is Required to Restrict Dendritic Complexity
34
Citations
39
References
2013
Year
Molecular RegulationMolecular BiologyNeurotransmissionDendritic ComplexityCellular PhysiologySocial SciencesDendritic ArborSignaling PathwayCell SignalingGtpase Rem2Restrict Dendritic ComplexityDendritic ArborizationMolecular NeuroscienceCamkii-dependent PhosphorylationG Protein-coupled ReceptorCortical RemodelingCell BiologySignal TransductionNeuroscienceMolecular NeurobiologyIntracellular TraffickingCellular BiochemistrySystems BiologyMedicineCentral Nervous System
The morphogenesis of the dendritic arbor is a critical aspect of neuronal development, ensuring that proper neural networks are formed. However, the molecular mechanisms that underlie this dendritic remodeling remain obscure. We previously established the activity-regulated GTPase Rem2 as a negative regulator of dendritic complexity. In this study, we identify a signaling pathway whereby Rem2 regulates dendritic arborization through interactions with Ca(2+)/calmodulin-dependent kinases (CaMKs) in rat hippocampal neurons. Specifically, we demonstrate that Rem2 functions downstream of CaMKII but upstream of CaMKIV in a pathway that restricts dendritic complexity. Furthermore, we show that Rem2 is a novel substrate of CaMKII and that phosphorylation of Rem2 by CaMKII regulates Rem2 function and subcellular localization. Overall, our results describe a unique signal transduction network through which Rem2 and CaMKs function to restrict dendritic complexity.
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