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

被引:85
作者
Gautron, Laurent [1 ,2 ]
Sakata, Ichiro [1 ,2 ]
Udit, Swalpa [1 ,2 ]
Zigman, Jeffrey M. [1 ,2 ]
Wood, John N. [3 ]
Elmquist, Joel K. [3 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Div Hypothalam Res, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Pharmacol, Div Hypothalam Res, Dallas, TX 75390 USA
[3] UCL, Wolfson Inst Biomed Res, London WC1E 6BT, England
基金
英国生物技术与生命科学研究理事会; 美国国家卫生研究院;
关键词
vagotomy; autonomic nervous system; transgenic; visceral pain; obesity; connections; INTRAGANGLIONIC LAMINAR ENDINGS; HEPATIC GLUCOSE-PRODUCTION; GLUCAGON-LIKE PEPTIDE-1; DORSAL-ROOT GANGLIA; RAT NODOSE GANGLION; GASTROINTESTINAL-TRACT; ENTEROENDOCRINE CELLS; FOOD-INTAKE; RECEPTOR IMMUNOREACTIVITY; SENSORY INNERVATION;
D O I
10.1002/cne.22667
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:3085 / 3101
页数:17
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