TRPV1 induction in airway vagal low-threshold mechanosensory neurons by allergen challenge and neurotrophic factors

被引:110
作者
Lieu, Tina Marie [1 ]
Myers, Allen C. [1 ]
Meeker, Sonya [1 ]
Undem, Bradley J. [1 ]
机构
[1] Johns Hopkins Univ Med Inst, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
asthma; C-fiber; capsaicin; vagus; NERVE GROWTH-FACTOR; GUINEA-PIG AIRWAYS; SENSORY NEURONS; RECEPTOR EXPRESSION; PHENOTYPIC SWITCH; GDNF FAMILY; INFLAMMATION; PROVOCATION; SENSITIVITY; ACTIVATION;
D O I
10.1152/ajplung.00366.2011
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Lieu T, Myers AC, Meeker S, Undem BJ. TRPV1 induction in airway vagal low-threshold mechanosensory neurons by allergen challenge and neurotrophic factors. Am J Physiol Lung Cell Mol Physiol 302: L941-L948, 2012. First published March 2, 2012; doi: 10.1152/ajplung.00366.2011.-We addressed the hypothesis that allergic inflammation in guinea pig airways leads to a phenotypic switch in vagal tracheal cough-causing, low-threshold mechanosensitive A delta neurons, such that they begin expressing functional transient receptor potential vanilloid (TRPV1) channels. Guinea pigs were actively sensitized to ovalbumin (OVA) and beginning 21 days later exposed via aerosol to OVA daily for 3 days. Tracheal-specific neurons were identified in the nodose ganglion using retrograde tracing techniques. Tracheal specific neurons were isolated, and mRNA expression was evaluated at the single-neuron level using RT-PCR analysis. Electrophysiological studies have revealed that the vast majority of vagal nodose afferent nerves innervating the trachea are capsaicin-insensitive A delta-fibers. Consistent with this, we found < 20% of these neurons express TRPV1 mRNA or respond to capsaicin in a calcium assay. Allergen exposure induced de novo TRPV1 mRNA in a majority of the tracheal-specific nodose neurons (P < 0.05). The allergen-induced TRPV1 induction was mimicked by applying either brain-derived neurotrophic factor (BDNF) or glial-derived neurotrophic factor (GDNF) to the tracheal lumen. The BDNF-induced phenotypic change observed at the level of mRNA expression was mimicked using a calcium assay to assess functional TRPV1 ion channels. Finally, OVA exposure induced BDNF and GDNF production in the tracheal epithelium, the immediate vicinity of the nodose A delta-fibers terminations. The induction of TRPV1 in nodose tracheal A delta-fibers would substantively expand the nature of stimuli capable of activating these cough-causing nerves.
引用
收藏
页码:L941 / L948
页数:8
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