4.5 Article

Genetic Tracing of Nav1.8-Expressing Vagal Afferents in the Mouse

期刊

JOURNAL OF COMPARATIVE NEUROLOGY
卷 519, 期 15, 页码 3085-3101

出版社

WILEY-BLACKWELL
DOI: 10.1002/cne.22667

关键词

vagotomy; autonomic nervous system; transgenic; visceral pain; obesity; connections

资金

  1. National Institutes of Health [PL1 DK081182, UL1 RR024923, NID DK088761-01, R01 DK53301, RL1 DK081185, RO1 DA024680]
  2. Biotechnology and Biological Sciences Research Council [BB/F000227/1] Funding Source: researchfish
  3. Medical Research Council [G0901905] Funding Source: researchfish
  4. BBSRC [BB/F000227/1] Funding Source: UKRI
  5. MRC [G0901905] Funding Source: UKRI

向作者/读者索取更多资源

Nav1.8 is a tetrodotoxin-resistant sodium channel present in large subsets of peripheral sensory neurons, including both spinal and vagal afferents. In spinal afferents, Nav1.8 plays a key role in signaling different types of pain. Little is known, however, about the exact identity and role of Nav1.8-expressing vagal neurons. Here we generated mice with restricted expression of tdTomato fluorescent protein in all Nav1.8-expressing afferent neurons. As a result, intense fluorescence was visible in the cell bodies, central relays, and sensory endings of these neurons, revealing the full extent of their innervation sites in thoracic and abdominal viscera. For instance, vagal and spinal Nav1.8-expressing endings were seen clearly within the gastrointestinal mucosa and myenteric plexus, respectively. In the gastrointestinal muscle wall, labeled endings included a small subset of vagal tension receptors but not any stretch receptors. We also examined the detailed innervation of key metabolic tissues such as liver and pancreas and evaluated the anatomical relationship of Nav1.8-expressing vagal afferents with select enteroendocrine cells (i.e., ghrelin, glucagon, GLP-1). Specifically, our data revealed the presence of Nav1.8-expressing vagal afferents in several metabolic tissues and varying degrees of proximity between Nav1.8-expressing mucosal afferents and enteroendocrine cells, including apparent neuroendocrine apposition. In summary, this study demonstrates the power and versatility of the Cre-LoxP technology to trace identified visceral afferents, and our data suggest a previously unrecognized role for Nav1.8-expressing vagal neurons in gastrointestinal functions. J. Comp. Neurol. 519:30853101, 2011. (C) 2011 Wiley-Liss, Inc.

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