Immunohistochemical Localization of Five Members of the K<sub>V</sub>1 Channel Subunits: Contrasting Subcellular Locations and Neuron‐specific Co‐localizations in Rat Brain

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<jats:title>Abstract</jats:title><jats:p>A large variety of potassium channels is involved in regulating integration and transmission of electrical signals in the nervous system. Different types of neurons, therefore, require specific patterns of potassium channel subunit expression and specific regulation of subunit coassembly into heteromultimeric channels, as well as subunit‐specific sorting and segregation. This was investigated by studying in detail the expression of six different α‐subunits of voltage‐gated potassium channels in the rat hippocampus, cerebellum, olfactory bulb and spinal cord, combining <jats:italic>in situ</jats:italic> hybridization and immunocytochemistry. Specific polyclonal antibodies were prepared for five α‐subunits (K<jats:sub>V</jats:sub>1.1, K<jats:sub>V</jats:sub>1.2, K<jats:sub>V</jats:sub>1.3, K<jats:sub>V</jats:sub>1.4, K<jats:sub>V</jats:sub>1.6) of the <jats:italic>Shaker</jats:italic>‐related subfamily of rat K<jats:sub>v</jats:sub> channels, which encode delayed‐rectifier type and rapidly inactivating A‐type potassium channels. Their distribution was compared to that of an A‐type potassium channel (K<jats:sub>V</jats:sub>3.4), belonging to the <jats:italic>Shaw</jats:italic>‐related subfamily of rat K<jats:sub>v</jats:sub> channels. Our results show that these K<jats:sub>v</jats:sub> channel α‐subunits are differentially expressed in rat brain neurons. We did not observe in various neurons a stereotypical distribution of K<jats:sub>v</jats:sub> channel α‐subunits to dendritic and axonal compartments, but a complex differential subcellular subunit distribution. The different K<jats:sub>v</jats:sub> channel subunits are targeted either to presynaptic or to postsynaptic domains, depending on neuronal cell type. Thus, distinct combinations of K<jats:sub>v</jats:sub>1 α‐subunits are co‐localized in different neurons. The implications of these findings are that both differential expression and assembly as well as subcellular targeting of K<jats:sub>v</jats:sub> channel α‐subunits may contribute to K<jats:sub>v</jats:sub> channel diversity and thereby to presynaptic and postsynaptic membrane excitability.</jats:p>

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