Lynn Therese M, Molloy Emer L, Masterson Joanne C, Glynn Senan F, Costello Richard W, Avdalovic Mark V, Schelegle Edward S, Miller Lisa A, Hyde Dallas M, O'Dea Shirley
1 Biology Department, Maynooth University, County Kildare, Ireland.
2 Department of Pediatrics, University of Colorado Denver, Aurora, Colorado.
Am J Respir Cell Mol Biol. 2016 Apr;54(4):562-73. doi: 10.1165/rcmb.2015-0210OC.
Bone morphogenetic protein (BMP) signaling is important for correct lung morphogenesis, and there is evidence of BMP signaling reactivation in lung diseases. However, little is known about BMP signaling patterns in healthy airway homeostasis and inflammatory airway disease and during epithelial repair. In this study, a rhesus macaque (Macaca mulatta) model of allergic airway disease was used to investigate BMP signaling throughout the airways in health, disease, and regeneration. Stereologic quantification of immunofluorescent images was used to determine the expression of BMP receptor (BMPR) Ia and phosphorylated SMAD (pSMAD) 1/5/8 in the airway epithelium. A pSMAD 1/5/8 expression gradient was found along the airways of healthy juvenile rhesus macaques (n = 3, P < 0.005). Membrane-localized BMPRIa expression was also present in the epithelium of the healthy animals. After exposure to house dust mite allergen and ozone, significant down-regulation of nuclear pSMAD 1/5/8 occurs in the epithelium. When the animals were provided with a recovery period in filtered air, proliferating cell nuclear antigen, pSMAD 1/5/8, and membrane-localized BMPRIa expression were significantly increased in the epithelium of conducting airways (P < 0.005). Furthermore, in the asthmatic airways, altered BMPRIa localization was evident. Because of the elevated eosinophil presence in these airways, we investigated the effect of eosinophil-derived proteins on BMPRIa trafficking in epithelial cells. Eosinophil-derived proteins (eosinophil-derived neurotoxin, eosinophil peroxidase, and major basic protein) induced transient nuclear translocation of membrane-bound BMPRIa. This work mapping SMAD signaling in the airways of nonhuman primates highlights a potential mechanistic relationship between inflammatory mediators and BMP signaling and provides evidence that basal expression of the BMP signaling pathway may be important for maintaining healthy airways.
骨形态发生蛋白(BMP)信号传导对正确的肺形态发生很重要,并且有证据表明BMP信号传导在肺部疾病中重新激活。然而,关于BMP信号传导在健康气道稳态、炎症性气道疾病以及上皮修复过程中的模式,人们了解甚少。在本研究中,使用恒河猴(猕猴)过敏性气道疾病模型来研究健康、疾病和再生过程中整个气道的BMP信号传导。通过对免疫荧光图像进行体视学定量,以确定气道上皮中BMP受体(BMPR)Ia和磷酸化SMAD(pSMAD)1/5/8的表达。在健康幼年恒河猴(n = 3,P < 0.005)的气道中发现了pSMAD 1/5/8表达梯度。膜定位的BMPRIa表达也存在于健康动物的上皮中。暴露于屋尘螨过敏原和臭氧后,上皮中核pSMAD 1/5/8显著下调。当动物在过滤空气中有恢复期时,传导气道上皮中的增殖细胞核抗原、pSMAD 1/5/8和膜定位的BMPRIa表达显著增加(P < 0.005)。此外,在哮喘气道中,BMPRIa定位改变明显。由于这些气道中嗜酸性粒细胞的存在增加,我们研究了嗜酸性粒细胞衍生蛋白对上皮细胞中BMPRIa转运的影响。嗜酸性粒细胞衍生蛋白(嗜酸性粒细胞衍生神经毒素、嗜酸性粒细胞过氧化物酶和主要碱性蛋白)诱导膜结合的BMPRIa发生短暂的核转位。这项在非人类灵长类动物气道中绘制SMAD信号传导的工作突出了炎症介质与BMP信号传导之间潜在的机制关系,并提供了证据表明BMP信号通路的基础表达可能对维持健康气道很重要。