Abstract

Axonal outgrowth and the formation of the axon initial segment (AIS) are early events in the acquisition of neuronal polarity. The AIS is characterized by a high concentration of voltage-dependent sodium and potassium channels. However, the specific ion channel subunits present and their precise localization in this axonal subdomain vary both during development and among the types of neurons, probably determining their firing characteristics in response to stimulation. Here, we characterize the developmental expression of different subfamilies of voltage-gated potassium channels in the AISs of cultured mouse hippocampal neurons, including subunits Kv1.2, Kv2.2 and Kv7.2. In contrast to the early appearance of voltage-gated sodium channels and the Kv7.2 subunit at the AIS, Kv1.2 and Kv2.2 subunits were tethered at the AIS only after 10 days in vitro. Interestingly, we observed different patterns of Kv1.2 and Kv2.2 subunit expression, with each confined to distinct neuronal populations. The accumulation of Kv1.2 and Kv2.2 subunits at the AIS was dependent on ankyrin G tethering, it was not affected by disruption of the actin cytoskeleton and it was resistant to detergent extraction, as described previously for other AIS proteins. This distribution of potassium channels in the AIS further emphasizes the heterogeneity of this structure in different neuronal populations, as proposed previously, and suggests corresponding differences in action potential regulation.

Highlights

  • The non-uniform distribution of specific of voltage-gated K+ (Kv) channels and their restriction to discrete neuronal domains is thought to contribute to the control of neuronal excitability

  • The present findings indicate that in contrast to the early expression of voltage-gated sodium channels (VGSC) and Kv7 potassium channels in the axon initial segment (AIS), Kv1.2 and Kv2.2 subunits are first tethered at the AIS of cultured hippocampal neurons after 10 days in vitro (DIV)

  • Our results show that the accumulation of Kv1.2 and Kv2.2 subunits in the AIS is resistant to detergent extraction and like other AIS proteins, it is dependent on the presence of ankyrin G

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Summary

Introduction

The non-uniform distribution of specific of voltage-gated K+ (Kv) channels and their restriction to discrete neuronal domains is thought to contribute to the control of neuronal excitability These channels are believed to influence different properties of neurons, including resting membrane potential, waveform shape, action potential (AP) firing pattern, transmitter release and synaptic strength. Kv channels are complexes made up of four voltage-sensing and pore-forming subunits, each generated from a family of over 35 subunits divided into 12 subfamilies (Kv1–12) [7,8] These complexes may assemble with auxiliary b subunits what may influence the expression, localization and biophysical properties of Kv channels [9,10,11]. Together with heterogeneous expression and localization of such channels in the AIS, they are likely to contribute to the electrophysiological variability between neuronal populations, and the corresponding differences in AP initiation and/or propagation [17,18,19,20,27,28,29,30,31]

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