Lung-innervating neurons expressingTmc3can induce broncho-constriction and dilation with direct consequences for the respiratory cycle

Abstract

AbstractSensory neurons of the vagal ganglia (VG) innervate lungs and play a critical role in maintaining airway homeostasis. However, the specific VG neurons that innervate lungs, and the mechanisms by which these neurons sense and respond to airway insults, are not well understood. Here, we identify a subpopulation of lung-innervating VG neurons defined by their expression ofTmc3. Single cell transcriptomics illuminated several subpopulations ofTmc3+sensory neurons, revealing distinctPiezo2- andTrpv1-expressing subclusters. Furthermore,Tmc3deficiency in VG neurons leads to global and subcluster specific transcriptional changes related to metabolic and ion channel function. Importantly, we show that broncho-constriction and dilation can be modulated through inhibition or activation ofTmc3+VG neurons resulting in a decrease or increase of end-expiratory lung volume, respectively. Together, our data show thatTmc3is a marker of lung-innervating neurons and may play a pivotal role in maintaining fundamental inspiratory and expiratory processes.SignificanceHarnessing the neuronal mechanisms that regulate lung function offers potential alternatives to existing corticosteroid treatment regimens for respiratory illness associated with acute bronchoconstriction including asthma, COPD, and emphysema. Our findings defineTransmembrane channel-like 3,Tmc3, as a marker of lung-innervating sensory neurons, identify distinct subpopulations ofTmc3+ neurons with unique transcriptional profiles, and show that activation or inhibition of these neurons has a significant impact on airway function. Our work highlights potential avenues of novel targeted intervention in respiratory conditions driven by dysfunctional neuronal reflexes.