Publication | Open Access
Localization of Kv1.1 and Kv1.2, two K channel proteins, to synaptic terminals, somata, and dendrites in the mouse brain
395
Citations
22
References
1994
Year
Synaptic TransmissionNeurotransmissionCellular NeurobiologySocial SciencesHyperpolarization (Biology)Channel ProteinsSynaptic TerminalsMolecular NeuroscienceIon ChannelsNervous SystemCell BiologySynaptic PlasticityNeurophysiologyNeuroanatomyK ChannelMultiple Voltage-gated PotassiumMammalian BrainMouse BrainNeuroscienceMolecular NeurobiologyCentral Nervous SystemMedicine
Voltage‑gated potassium channels are thought to regulate neuronal excitability in the mammalian brain. mKv1.1 and mKv1.2 are found in multiple subcellular compartments—somata, axons, synaptic terminals, and dendrites—with region‑specific expression patterns that may influence neuronal excitability.
Multiple voltage-gated potassium (K) channel gene products are likely to be involved in regulating neuronal excitability of any single neuron in the mammalian brain. Here we show that two closely related voltage-gated K channel proteins, mKv1.1 and mKv1.2, are present in multiple subcellular locations including cell somata, juxta-paranodal regions of myelinated axons, synaptic terminals, unmyelinated axons, specialized junctions among axons, and proximal dendrites. Staining patterns of the two channel polypeptides overlap in some areas of the brain, yet each has a unique pattern of expression. For example, in the hippocampus, both mKv1.1 and mKv1.2 proteins are present in axons, often near or at synaptic terminals in the middle molecular layer of the dentate gyrus, while only mKv1.1 is detected in axons and synaptic terminals in the hilar/CA3 region. In the cerebellum, both channel proteins are localized to axon terminals and specialized junctions among axons in the plexus region of basket cells. Strong differential staining is observed in the olfactory bulb, where mKv1.2 is localized to cell somata and axons, as well as to proximal dendrites of the mitral cells. This overlapping yet differential pattern of expression and specific subcellular localization may contribute to the unique profile of excitability displayed by a particular neuron.
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