Department of Clinical Sciences, Faculty of Veterinary Medicine, Université de Montréal, Saint-Hyacinthe, Quebec, Canada.
PLoS One. 2012;7(1):e29440. doi: 10.1371/journal.pone.0029440. Epub 2012 Jan 3.
Gene expression analyses are used to investigate signaling pathways involved in diseases. In asthma, they have been primarily derived from the analysis of bronchial biopsies harvested from mild to moderate asthmatic subjects and controls. Due to ethical considerations, there is currently limited information on the transcriptome profile of the peripheral lung tissues in asthma.
To identify genes contributing to chronic inflammation and remodeling in the peripheral lung tissue of horses with heaves, a naturally occurring asthma-like condition.
Eleven adult horses (6 heaves-affected and 5 controls) were studied while horses with heaves were in clinical remission (Pasture), and during disease exacerbation induced by a 30-day natural antigen challenge during stabling (Challenge). Large peripheral lung biopsies were obtained by thoracoscopy at both time points. Using suppression subtractive hybridization (SSH), lung cDNAs of controls (Pasture and Challenge) and asymptomatic heaves-affected horses (Pasture) were subtracted from cDNAs of horses with heaves in clinical exacerbation (Challenge). The differential expression of selected genes of interest was confirmed using quantitative PCR assay.
Horses with heaves, but not controls, developed airway obstruction when challenged. Nine hundred and fifty cDNA clones isolated from the subtracted library were screened by dot blot array and 224 of those showing the most marked expression differences were sequenced. The gene expression pattern was confirmed by quantitative PCR in 15 of 22 selected genes. Novel genes and genes with an already defined function in asthma were identified in the subtracted cDNA library. Genes of particular interest associated with asthmatic airway inflammation and remodeling included those related to PPP3CB/NFAT, RhoA, and LTB4/GPR44 signaling pathways.
Pathways representing new possible targets for anti-inflammatory and anti-remodeling therapies for asthma were identified. The findings of genes previously associated with asthma validate this equine model for gene expression studies.
基因表达分析被用于研究与疾病相关的信号通路。在哮喘中,这些分析主要来自于对轻度至中度哮喘患者和对照者支气管活检的分析。由于伦理考虑,目前关于哮喘患者外周肺组织转录组谱的信息有限。
鉴定导致马气喘(一种自然发生的哮喘样疾病)外周肺组织慢性炎症和重塑的基因。
11 匹成年马(6 匹气喘受影响和 5 匹对照)在气喘受影响的马处于临床缓解期(牧场)时以及在圈养期间进行为期 30 天的自然抗原挑战导致疾病加重时(挑战)进行了研究。在这两个时间点,通过胸腔镜获得了大的外周肺活检。使用抑制性消减杂交(SSH),将对照(牧场和挑战)和无症状气喘受影响的马(牧场)的肺 cDNA 从临床加重的气喘马(挑战)的 cDNA 中减去。使用定量 PCR 检测选择的感兴趣基因的差异表达。
气喘马但不是对照马在受到挑战时会发生气道阻塞。从消减文库中筛选出 950 个 cDNA 克隆,并用斑点印迹阵列进行筛选,其中 224 个显示最明显表达差异的 cDNA 进行测序。在 22 个选定基因中,有 15 个通过定量 PCR 确认了基因表达模式。在消减 cDNA 文库中鉴定出了新的基因和已定义的哮喘相关功能的基因。与哮喘气道炎症和重塑相关的特别感兴趣的基因包括与 PPP3CB/NFAT、RhoA 和 LTB4/GPR44 信号通路相关的基因。
鉴定出了代表哮喘抗炎和抗重塑治疗新的可能靶点的通路。先前与哮喘相关的基因的发现验证了这种用于基因表达研究的马模型。