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Dissecting the Interoception Circuit that Controls Airway Constriction

剖析控制气道收缩的内感受回路

基本信息

批准号：
10320714
负责人：
Xin Sun
金额：
$ 55.53万
依托单位：
UNIVERSITY OF CALIFORNIA, SAN DIEGO
依托单位国家：
美国
项目类别：
财政年份：
2021
资助国家：
美国
起止时间：
2021-09-01 至 2026-08-31
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10320714
关键词：
Ablation Address Adult Aerosols Afferent Neurons Air Airway Disease Allergens Anxiety Asthma Back Brain Brain Stem Brain region Breathing Cell Nucleus Child Chronic Data Dementia Disease Efferent Neurons Electrophysiology (science)Epithelial Foundations Ganglia Gases Genetic Health system Human Hypothalamic structure Imaging Device In Situ Individual Injections Interoception Irritants Knowledge Label Link Lung Maps Meditation Mental Depression Molecular Nerve Nervous system structure Neuraxis Neuroendocrine Cell Neurons Nucleus solitarius Organ Peripheral Physiology Property Psyche structure Qi Gong RNA Recombinant adeno-associated virus (rAAV)Respiration Sensory Side Signal Transduction Smooth Muscle Spinal Spinal Cord Spinal cord posterior horn Stress Suggestion Synapses Techniques Testing Three-Dimensional Imaging Toxin Tube Vagotomy Viral airway hyperresponsiveness asthma exacerbation attenuation base cell type constriction dorsal motor nucleus expectation experimental study functional loss improved in vivo in vivo calcium imaging insight mouse allergen mouse model neural circuit neuronal cell body novel therapeutics optical imaging optogenetics paraventricular nucleus prevent pulmonary function relating to nervous system respiratory response sensor spatial relationship tool

项目摘要

PROJECT SUMMARY/ABSTRACT Lung is one of the largest internal sensory organs. Chronic exposure of the lung to allergens or other irritants has been shown to influence stress, anxiety, depression, and dementia. On the other hand, practices that modulate respiration including deep breathing in meditation or Qi Gong are linked to improved central nervous system (CNS) health. However, the functional neuroanatomical connections between brain and lung at the molecular and cellular level remain largely unknown. This R01 application proposes to test the hypothesis, using mouse models, that allergen-induced signals detected by interoceptors in the lung are transmitted via vagal afferent neurons to nucleus tractus solitarius (NTS) (aim 1), and then from NTS to other central integrators in the brain, potentially including paraventricular nucleus (PVH) in the hypothalamus (aim 2), and lastly from dorsal motor nucleus of the vagus (DMV) to descending spinal cord efferents that project back to the lung (aim 3) to sense and regulate airway hyperresponsiveness. The aims will incorporate cutting-edge cell-type specific circuit and viral tracing techniques, lightsheet 3-D imaging, and candidate multiplex RNA in situ and unbiased snRNAseq approaches to map the neural circuits and identify the signature of signal-activated neurons in peripheral ganglia, NTS and other brain regions. In addition, they will combine chemogenetic, optogenetic and toxin-based approaches with neural activity readouts including cFOS, in vivo calcium imaging, electrophysiology, and lung physiology to assess gain and loss of functional effects of key lung, vagal, spinal and brain connections.

项目总结/文摘