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Front Cell Neurosci. 2019 Jan 22;13:1. doi: 10.3389/fncel.2019.00001. eCollection 2019.

Loss of Neurofascin-186 Disrupts Alignment of AnkyrinG Relative to Its Binding Partners in the Axon Initial Segment.

Author information

1
Department of Biological Sciences, Dartmouth College, Hanover, NH, United States.
2
Department of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth College, Hanover, NH, United States.

Abstract

The axon initial segment (AIS) is a specialized region within the proximal portion of the axon that initiates action potentials thanks in large part to an enrichment of sodium channels. The scaffolding protein ankyrinG (AnkG) is essential for the recruitment of sodium channels as well as several other intracellular and extracellular proteins to the AIS. In the present study, we explore the role of the cell adhesion molecule (CAM) neurofascin-186 (NF-186) in arranging the individual molecular components of the AIS in cultured rat hippocampal neurons. Using a CRISPR depletion strategy to ablate NF expression, we found that the loss of NF selectively perturbed AnkG accumulation and its relative proximal distribution within the AIS. We found that the overexpression of sodium channels could restore AnkG accumulation, but not its altered distribution within the AIS without NF present. We go on to show that although the loss of NF altered AnkG distribution, sodium channel function within the AIS remained normal. Taken together, these results demonstrate that the regulation of AnkG and sodium channel accumulation within the AIS can occur independently of one another, potentially mediated by other binding partners such as NF.

KEYWORDS:

ankyrin G; axon initial segment; cultured hippocampal neurons; neurofascin-186; voltage gated sodium channels

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