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Polysialic Acid Regulates Sympathetic Outflow by Facilitating Information Transfer within the Nucleus of the Solitary Tract.
Bokiniec, Phillip; Shahbazian, Shila; McDougall, Stuart J; Berning, Britt A; Cheng, Delfine; Llewellyn-Smith, Ida J; Burke, Peter G R; McMullan, Simon; Mühlenhoff, Martina; Hildebrandt, Herbert; Braet, Filip; Connor, Mark; Packer, Nicolle H; Goodchild, Ann K.
Affiliation
  • Bokiniec P; Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, 2109 New South Wales, Australia.
  • Shahbazian S; Max Delbrück Center for Molecular Medicine, Robert-Roessle-Str. 10, Berlin, 13092, Germany.
  • McDougall SJ; Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, 2109 New South Wales, Australia.
  • Berning BA; Florey Institute of Neuroscience and Mental Health, University of Melbourne, Melbourne, 3010 Victoria, Australia.
  • Cheng D; Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, 2109 New South Wales, Australia.
  • Llewellyn-Smith IJ; School of Medical Sciences, Discipline of Anatomy and Histology, University of Sydney, Sydney, 2006 New South Wales, Australia.
  • Burke PGR; Cardiovascular Medicine and Human Physiology, Flinders University, Adelaide, 5042 South Australia, Australia.
  • McMullan S; Neuroscience Research Australia, Sydney, 2031 New South Wales, Australia.
  • Mühlenhoff M; Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, 2109 New South Wales, Australia.
  • Hildebrandt H; Institut für Zelluläre Chemie, Medizinische Hochschule Hannover, Hannover 30625, Germany.
  • Braet F; Institut für Zelluläre Chemie, Medizinische Hochschule Hannover, Hannover 30625, Germany.
  • Connor M; School of Medical Sciences, Discipline of Anatomy and Histology, University of Sydney, Sydney, 2006 New South Wales, Australia.
  • Packer NH; Australian Centre for Microscopy and Microanalysis, University of Sydney, Sydney, 2006 New South Wales, Australia.
  • Goodchild AK; Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, 2109 New South Wales, Australia.
J Neurosci ; 37(27): 6558-6574, 2017 07 05.
Article in En | MEDLINE | ID: mdl-28576943
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sialic Acids / Sympathetic Nervous System / Afferent Pathways / Solitary Nucleus / Nerve Net / Neuronal Plasticity Type of study: Prognostic_studies Limits: Animals Language: En Journal: J Neurosci Year: 2017 Document type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sialic Acids / Sympathetic Nervous System / Afferent Pathways / Solitary Nucleus / Nerve Net / Neuronal Plasticity Type of study: Prognostic_studies Limits: Animals Language: En Journal: J Neurosci Year: 2017 Document type: Article Affiliation country: Australia