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通过特定的迷走神经和背根神经节神经元亚群对小鼠肺感觉神经支配的定位。

Mapping of the Sensory Innervation of the Mouse Lung by Specific Vagal and Dorsal Root Ganglion Neuronal Subsets.

机构信息

Molecular Pharmacology and Physiology, Morsani College of Medicine, University of South Florida, Tampa, FL 33612.

Molecular Pharmacology and Physiology, Morsani College of Medicine, University of South Florida, Tampa, FL 33612

出版信息

eNeuro. 2022 Apr 13;9(2). doi: 10.1523/ENEURO.0026-22.2022. Print 2022 Mar-Apr.

Abstract

The airways are densely innervated by sensory afferent nerves, whose activation regulates respiration and triggers defensive reflexes (e.g., cough, bronchospasm). Airway innervation is heterogeneous, and distinct afferent subsets have distinct functional responses. However, little is known of the innervation patterns of subsets within the lung. A neuroanatomical map is critical for understanding afferent activation under physiological and pathophysiological conditions. Here, we quantified the innervation of the mouse lung by vagal and dorsal root ganglion (DRG) sensory subsets defined by the expression of Pirt (all afferents), 5HT (vagal nodose afferents), Tac1 (tachykinergic afferents), and transient receptor potential vanilloid 1 channel (TRPV1; defensive/nociceptive afferents) using Cre-mediated reporter expression. We found that vagal afferents innervate almost all conducting airways and project into the alveolar region, whereas DRG afferents only innervate large airways. Of the two vagal ganglia, only nodose afferents project into the alveolar region, but both nodose and jugular afferents innervate conducting airways throughout the lung. Many afferents that project into the alveolar region express TRPV1. Few DRG afferents expressed TRPV1. Approximately 25% of blood vessels were innervated by vagal afferents (many were Tac1+). Approximately 10% of blood vessels had DRG afferents (some were Tac1+), but this was restricted to large vessels. Lastly, innervation of neuroepithelial bodies (NEBs) correlated with the cell number within the bodies. In conclusion, functionally distinct sensory subsets have distinct innervation patterns within the conducting airways, alveoli and blood vessels. Physiologic (e.g., stretch) and pathophysiological (e.g., inflammation, edema) stimuli likely vary throughout these regions. Our data provide a neuroanatomical basis for understanding afferent responses .

摘要

气道被感觉传入神经密集地支配,其激活调节呼吸并引发防御反射(例如咳嗽、支气管痉挛)。气道神经支配是异质的,不同的传入神经子集具有不同的功能反应。然而,肺内传入神经子集的支配模式知之甚少。神经解剖图谱对于理解生理和病理生理条件下传入神经的激活至关重要。在这里,我们通过 Pirt(所有传入神经)、5HT(迷走神经结状传入神经)、Tac1(速激肽能传入神经)和瞬时受体电位香草酸 1 通道(TRPV1;防御/伤害性传入神经)表达定义的迷走神经和背根神经节(DRG)感觉亚群,定量分析了小鼠肺的神经支配。我们发现迷走神经传入神经几乎支配所有传导气道并投射到肺泡区域,而 DRG 传入神经仅支配大气道。在两个迷走神经节中,只有结状传入神经投射到肺泡区域,但结状和颈静脉传入神经都支配整个肺的传导气道。许多投射到肺泡区域的传入神经表达 TRPV1。很少有 DRG 传入神经表达 TRPV1。大约 25%的血管被迷走神经传入神经支配(许多是 Tac1+)。大约 10%的血管有 DRG 传入神经(有些是 Tac1+),但仅限于大血管。最后,神经上皮体(NEBs)的支配与体内细胞数量相关。总之,功能不同的感觉亚群在传导气道、肺泡和血管中有不同的支配模式。生理(例如,拉伸)和病理生理(例如,炎症、水肿)刺激可能在这些区域内有所不同。我们的数据为理解传入神经反应提供了神经解剖学基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71a5/9015009/50bad30a27c3/ENEURO.0026-22.2022_f001.jpg

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