Department of Respiratory Medicine and Exercise Physiology, The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Rm 209 Martin Research Building, 1124 West Carson Street, Torrance, CA, 90502, USA.
Department of Physiology and Pharmacology, Alberta Children's Hospital Research Institute, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Rm 203 Heritage Medical Research Building, 3330 Hospital Drive NW, Calgary, Alberta, T2N 4N1, Canada.
J Neuroinflammation. 2021 Aug 31;18(1):191. doi: 10.1186/s12974-021-02241-9.
The carotid bodies are multimodal sensors that regulate various autonomic reflexes. Recent evidence demonstrates their role in immune reflex regulation. Our previous studies using the allergen (ovalbumin) sensitised and exposed Brown Norway rat model of asthma suggest that carotid bodies mediate asthmatic bronchoconstriction through a lysophosphatidic acid (LPA) receptor (LPAr)-protein kinase C epsilon (PKCε)-transient receptor potential vanilloid one channel (TRPV1) pathway. Whilst naïve carotid bodies respond to LPA, whether their response to LPA is enhanced in asthma is unknown. Here, we show that asthmatic sensitisation of Brown Norway rats involving repeated aerosolised allergen challenges over 6 days, results in an augmentation of the carotid bodies' acute sensitivity to LPA. Increased expression of LPAr in the carotid bodies and petrosal ganglia likely contributed to this sensitivity. Importantly, allergen sensitisation of the carotid bodies to LPA did not alter their hypoxic response, nor did hypoxia augment LPA sensitivity acutely. Our data demonstrate the ability of allergens to sensitise the carotid bodies, highlighting the likely role of the carotid bodies and blood-borne inflammatory mediators in asthma.
颈动脉体是一种多模式传感器,可调节各种自主反射。最近的证据表明,它们在免疫反射调节中起作用。我们之前使用过敏原(卵清蛋白)致敏并暴露于哮喘的褐家鼠模型的研究表明,颈动脉体通过溶血磷脂酸(LPA)受体(LPAr)-蛋白激酶 C ɛ(PKCε)-瞬时受体电位香草酸 1 通道(TRPV1)途径介导哮喘性支气管痉挛。虽然未致敏的颈动脉体对 LPA 有反应,但它们对 LPA 的反应是否在哮喘中增强尚不清楚。在这里,我们表明,涉及重复雾化过敏原挑战 6 天的褐家鼠哮喘致敏导致颈动脉体对 LPA 的急性敏感性增强。颈动脉体和耳神经节中 LPAr 的表达增加可能促成了这种敏感性。重要的是,过敏原对颈动脉体对 LPA 的致敏作用并未改变其对缺氧的反应,也没有急性增加缺氧对 LPA 的敏感性。我们的数据表明过敏原能够使颈动脉体致敏,这突出了颈动脉体和血液源性炎症介质在哮喘中的可能作用。