Characterization of the axon initial segment of mice substantia nigra dopaminergic neurons.

Journal Article (Journal Article)

The axon initial segment (AIS) is the site of initiation of action potentials and influences action potential waveform, firing pattern, and rate. In view of the fundamental aspects of motor function and behavior that depend on the firing of substantia nigra pars compacta (SNc) dopaminergic neurons, we identified and characterized their AIS in the mouse. Immunostaining for tyrosine hydroxylase (TH), sodium channels (Nav ) and ankyrin-G (Ank-G) was used to visualize the AIS of dopaminergic neurons. Reconstructions of sampled AIS of dopaminergic neurons revealed variable lengths (12-60 μm) and diameters (0.2-0.8 μm), and an average of 50% reduction in diameter between their widest and thinnest parts. Ultrastructural analysis revealed submembranous localization of Ank-G at nodes of Ranvier and AIS. Serial ultrathin section analysis and 3D reconstructions revealed that Ank-G colocalized with TH only at the AIS. Few cases of synaptic innervation of the AIS of dopaminergic neurons were observed. mRNA in situ hybridization of brain-specific Nav subunits revealed the expression of Nav 1.2 by most SNc neurons and a small proportion expressing Nav 1.6. The presence of sodium channels, along with the submembranous location of Ank-G is consistent with the role of AIS in action potential generation. Differences in the size of the AIS likely underlie differences in firing pattern, while the tapering diameter of AIS may define a trigger zone for action potentials. Finally, the conspicuous expression of Nav 1.2 by the majority of dopaminergic neurons may explain their high threshold for firing and their low discharge rate.

Full Text

Duke Authors

Cited Authors

  • González-Cabrera, C; Meza, R; Ulloa, L; Merino-Sepúlveda, P; Luco, V; Sanhueza, A; Oñate-Ponce, A; Bolam, JP; Henny, P

Published Date

  • November 1, 2017

Published In

Volume / Issue

  • 525 / 16

Start / End Page

  • 3529 - 3542

PubMed ID

  • 28734032

Pubmed Central ID

  • 28734032

Electronic International Standard Serial Number (EISSN)

  • 1096-9861

Digital Object Identifier (DOI)

  • 10.1002/cne.24288

Language

  • eng

Conference Location

  • United States