Madigan Laura A, Wong Gordon S, Gordon Elizabeth M, Chen Wei-Sheng, Balenga Nariman, Koziol-White Cynthia J, Panettieri Reynold A, Levine Stewart J, Druey Kirk M
1 Molecular Signal Transduction Section, Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, and.
2 Laboratory of Asthma and Lung Inflammation, Cardiovascular and Pulmonary Branch, Division of Intramural Research, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland; and.
Am J Respir Cell Mol Biol. 2018 Jan;58(1):89-98. doi: 10.1165/rcmb.2017-0109OC.
A cardinal feature of asthma is airway hyperresponsiveness (AHR) to spasmogens, many of which activate G protein-coupled receptors (GPCRs) on airway smooth muscle (ASM) cells. Asthma subtypes associated with allergy are characterized by eosinophilic inflammation in the lung due to the type 2 immune response to allergens and proinflammatory mediators that promote AHR. The degree to which intrinsic abnormalities of ASM contribute to this phenotype remains unknown. The regulators of G protein signaling (RGS) proteins are a large group of intracellular proteins that inhibit GPCR signaling pathways. RGS2- and RGS5-deficient mice develop AHR spontaneously. Although RGS4 is upregulated in ASM from patients with severe asthma, the effects of increased RGS4 expression on AHR in vivo are unknown. Here, we examined the impact of forced RGS4 overexpression in lung on AHR using transgenic (Tg) mice. Tg RGS4 was expressed in bronchial epithelium and ASM in vivo, and protein expression in lung was increased at least 4-fold in Tg mice compared with wild-type (WT) mice. Lung slices from Tg mice contracted less in response to the m3 muscarinic receptor agonist methacholine compared with the WT, although airway resistance in live, unchallenged mice of both strains was similar. Tg mice were partially protected against AHR induced by fungal allergen challenge due to weakened contraction signaling in ASM and reduced type 2 cytokine (IL-5 and IL-13) levels in Tg mice compared with the WT. These results provide support for the hypothesis that increasing RGS4 expression and/or function could be a viable therapeutic strategy for asthma.
哮喘的一个主要特征是气道对痉挛原的高反应性(AHR),其中许多痉挛原可激活气道平滑肌(ASM)细胞上的G蛋白偶联受体(GPCR)。与过敏相关的哮喘亚型的特征是,由于对过敏原和促炎介质的2型免疫反应导致肺部嗜酸性粒细胞炎症,而这些介质会促进AHR。ASM的内在异常对该表型的影响程度尚不清楚。G蛋白信号调节(RGS)蛋白是一大类抑制GPCR信号通路的细胞内蛋白。RGS2和RGS5缺陷型小鼠会自发出现AHR。尽管在重度哮喘患者的ASM中RGS4上调,但RGS4表达增加对体内AHR的影响尚不清楚。在这里,我们使用转基因(Tg)小鼠研究了肺中强制过表达RGS4对AHR的影响。Tg RGS4在体内的支气管上皮和ASM中表达,与野生型(WT)小鼠相比,Tg小鼠肺中的蛋白表达增加了至少4倍。与WT相比,Tg小鼠的肺切片对m3毒蕈碱受体激动剂乙酰甲胆碱的反应收缩较小,尽管两种品系的未受刺激的活体小鼠的气道阻力相似。与WT相比,Tg小鼠由于ASM中的收缩信号减弱和Tg小鼠中2型细胞因子(IL-5和IL-13)水平降低,对真菌过敏原激发诱导的AHR有部分保护作用。这些结果支持了增加RGS4表达和/或功能可能是一种可行的哮喘治疗策略这一假说。