Departments of Human Genetics, Montreal Children’s Hospital Research Institute, McGill University, Montreal, Quebec, Canada.
Am J Physiol Lung Cell Mol Physiol. 2012 Nov 15;303(10):L899-911. doi: 10.1152/ajplung.00179.2012. Epub 2012 Sep 14.
The "fetal origins hypothesis" argued that physiological changes consequent to in utero exposures ultimately contribute to disease susceptibility in later life. The dramatic increase in asthma prevalence is attributed to early exposures acting on preexisting asthma-susceptible genotypes. We showed previously that distinct transcriptome signatures distinguish the developmental respiratory phenotype of atopic (Brown Norway, BN) and normoresponsive (Lewis) rats. We aimed to determine whether maternal allergen exposure would influence asthma pathogenesis by reprogramming primary patterns of developmental lung gene expression. Postnatal offspring of dams sensitized to ovalbumin before mating and challenged during pregnancy were assessed for lung function, inflammatory biomarkers, and respiratory gene expression. Although maternal ovalbumin exposure resulted in characteristic features of an allergic response (bronchoalveolar lavage neutrophils, IgE, methacholine-induced lung resistance) in offspring of both strains, substantial strain-specific differences were observed in respiratory gene expression. Of 799 probes representing the top 5% of transcriptomic variation, only 112 (14%) were affected in both strains. Strain-specific gene signatures also exhibited marked differences in enrichment for gene ontologies, with immune regulation and cell proliferation being prominent in the BN strain, cell cycle and microtubule assembly gene sets in the Lewis strain. Multiple ovalbumin-specific probes in both strains were also differentially expressed in lymphoblastoid cell lines from human asthmatic vs. nonasthmatic sibling pairs. Our data point to the existence of distinct, genetically programmed responses to maternal exposures in developing lung. These different response patterns, if recapitulated in human fetal development, can contribute to long-term pulmonary health including interindividual susceptibility to asthma.
“胎儿起源假说”认为,子宫内暴露引起的生理变化最终导致生命后期的疾病易感性。哮喘患病率的急剧增加归因于早期暴露作用于预先存在的哮喘易感基因型。我们之前表明,不同的转录组特征区分了特应性(布朗诺威,BN)和正常反应性(刘易斯)大鼠的发育性呼吸表型。我们旨在确定母体过敏原暴露是否通过重新编程发育中肺基因表达的主要模式来影响哮喘发病机制。在交配前致敏卵清蛋白并在怀孕期间进行挑战的母鼠的后代进行肺功能、炎症生物标志物和呼吸基因表达评估。尽管母源性卵清蛋白暴露导致两种品系后代均具有过敏反应的特征(支气管肺泡灌洗中性粒细胞、IgE、乙酰甲胆碱诱导的肺阻力),但在呼吸基因表达方面观察到明显的品系特异性差异。在代表转录组变化前 5%的 799 个探针中,只有 112 个(14%)在两种品系中受到影响。基因特征也表现出基因本体论富集的明显差异,BN 品系中以免疫调节和细胞增殖为主,Lewis 品系中以细胞周期和微管组装基因集为主。两种品系中的多个卵清蛋白特异性探针在哮喘和非哮喘同胞对的淋巴母细胞系中也表现出差异表达。我们的数据表明,在发育中的肺中存在对母体暴露的独特的、遗传编程的反应。如果这些不同的反应模式在人类胎儿发育中重现,则可能导致长期的肺部健康,包括对哮喘的个体易感性。