Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/124389
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Type: Journal article
Title: Polysialic acid regulates sympathetic outflow by facilitating information transfer within the nucleus of the solitary tract
Author: Bokiniec, P.
Shahbazian, S.
McDougall, S.J.
Berning, B.A.
Cheng, D.
Llewellyn-Smith, I.J.
Burke, P.G.R.
McMullan, S.
Mühlenhoff, M.
Hildebrandt, H.
Braet, F.
Connor, M.
Packer, N.H.
Goodchild, A.K.
Citation: The Journal of Neuroscience, 2017; 37(27):6558-6574
Publisher: Society for Neuroscience
Issue Date: 2017
ISSN: 0270-6474
1529-2401
Statement of
Responsibility: 
Phillip Bokiniec, Shila Shahbazian, Stuart J. McDougall, Britt A. Berning, Delfine Cheng, Ida J. Llewellyn-Smith ... et al.
Abstract: Expression of the large extracellular glycan, polysialic acid (polySia), is restricted in the adult, to brain regions exhibiting high levels of plasticity or remodeling, including the hippocampus, prefrontal cortex, and the nucleus of the solitary tract (NTS). The NTS, located in the dorsal brainstem, receives constant viscerosensory afferent traffic as well as input from central regions controlling sympathetic nerve activity, respiration, gastrointestinal functions, hormonal release, and behavior. Our aims were to determine the ultrastructural location of polySia in the NTS and the functional effects of enzymatic removal of polySia, both in vitro and in vivo polySia immunoreactivity was found throughout the adult rat NTS. Electron microscopy demonstrated polySia at sites that influence neurotransmission: the extracellular space, fine astrocytic processes, and neuronal terminals. Removing polySia from the NTS had functional consequences. Whole-cell electrophysiological recordings revealed altered intrinsic membrane properties, enhancing voltage-gated K+ currents and increasing intracellular Ca2+ Viscerosensory afferent processing was also disrupted, dampening low-frequency excitatory input and potentiating high-frequency sustained currents at second-order neurons. Removal of polySia in the NTS of anesthetized rats increased sympathetic nerve activity, whereas functionally related enzymes that do not alter polySia expression had little effect. These data indicate that polySia is required for the normal transmission of information through the NTS and that changes in its expression alter sympathetic outflow. polySia is abundant in multiple but discrete brain regions, including sensory nuclei, in both the adult rat and human, where it may regulate neuronal function by mechanisms identified here.SIGNIFICANCE STATEMENT All cells are coated in glycans (sugars) existing predominantly as glycolipids, proteoglycans, or glycoproteins formed by the most complex form of posttranslational modification, glycosylation. How these glycans influence brain function is only now beginning to be elucidated. The adult nucleus of the solitary tract has abundant polysialic acid (polySia) and is a major site of integration, receiving viscerosensory information which controls critical homeostatic functions. Our data reveal that polySia is a determinant of neuronal behavior and excitatory transmission in the nucleus of the solitary tract, regulating sympathetic nerve activity. polySia is abundantly expressed at distinct brain sites in adult, including major sensory nuclei, suggesting that sensory transmission may also be influenced via mechanisms described here. These findings hint at the importance of elucidating how other glycans influence neural function.
Keywords: Electron microscopy; nucleus of the solitary tract; patch clamp; polysialic acid; sympathetic nerve activity; viscerosensory afferents
Rights: © 2017 the authors. Authors grant JNeurosci a license to publish their work and copyright remains with the author. For articles published after 2014, the Society for Neuroscience (SfN) retains an exclusive license to publish the article for 6 months; after 6 months, the work becomes available to the public to copy, distribute, or display under the terms of the Creative Commons Attribution 4.0 International License (CC-BY). This license allows data and text mining, use of figures in presentations, and posting the article online, provided that the original article is credited.
DOI: 10.1523/JNEUROSCI.0200-17.2017
Grant ID: http://purl.org/au-research/grants/nhmrc/APP1028183
http://purl.org/au-research/grants/nhmrc/APP1030301
http://purl.org/au-research/grants/arc/DP120100920
Published version: http://dx.doi.org/10.1523/jneurosci.0200-17.2017
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