共 111 条
Expression analysis of asthma candidate genes during human and murine lung development
被引:49
作者:

Melen, Erik
论文数: 0 引用数: 0
h-index: 0
机构:
Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USA
Karolinska Inst, Inst Environm Med, S-10401 Stockholm, Sweden
Karolinska Univ Hosp, Astrid Lindgren Childrens Hosp, Stockholm, Sweden Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA

Kho, Alvin T.
论文数: 0 引用数: 0
h-index: 0
机构:
Childrens Hosp, Informat Program, Boston, MA 02115 USA Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA

Sharma, Sunita
论文数: 0 引用数: 0
h-index: 0
机构:
Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USA
Brigham & Womens Hosp, Div Pulm & Crit Care Med, Boston, MA 02115 USA Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA

Gaedigk, Roger
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h-index: 0
机构:
Childrens Mercy Hosp & Clin, Dept Pediat, Div Clin Pharmacol & Med Toxicol, Kansas City, MO USA Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA

Leeder, J. Steven
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h-index: 0
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Childrens Mercy Hosp & Clin, Dept Pediat, Div Clin Pharmacol & Med Toxicol, Kansas City, MO USA Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA

Mariani, Thomas J.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Rochester, Div Neonatol, Rochester, NY USA
Univ Rochester, Ctr Pediat Biomed Res, Rochester, NY USA Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA

Carey, Vincent J.
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h-index: 0
机构:
Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USA Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA

Weiss, Scott T.
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h-index: 0
机构:
Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USA
Brigham & Womens Hosp, Div Pulm & Crit Care Med, Boston, MA 02115 USA
Partners Ctr Personalized Genet Med, Boston, MA USA Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA

Tantisira, Kelan G.
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h-index: 0
机构:
Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USA
Brigham & Womens Hosp, Div Pulm & Crit Care Med, Boston, MA 02115 USA
Partners Ctr Personalized Genet Med, Boston, MA USA Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA
机构:
[1] Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Karolinska Inst, Inst Environm Med, S-10401 Stockholm, Sweden
[4] Karolinska Univ Hosp, Astrid Lindgren Childrens Hosp, Stockholm, Sweden
[5] Childrens Hosp, Informat Program, Boston, MA 02115 USA
[6] Brigham & Womens Hosp, Div Pulm & Crit Care Med, Boston, MA 02115 USA
[7] Childrens Mercy Hosp & Clin, Dept Pediat, Div Clin Pharmacol & Med Toxicol, Kansas City, MO USA
[8] Univ Rochester, Div Neonatol, Rochester, NY USA
[9] Univ Rochester, Ctr Pediat Biomed Res, Rochester, NY USA
[10] Partners Ctr Personalized Genet Med, Boston, MA USA
来源:
RESPIRATORY RESEARCH
|
2011年
/
12卷
基金:
美国国家卫生研究院;
关键词:
Asthma;
Development;
Expression;
Genetics;
Lung;
SINGLE-NUCLEOTIDE POLYMORPHISM;
ACTIVATOR INHIBITOR-1 PAI-1;
BRONCHIAL EPITHELIAL-CELLS;
GENOME-WIDE ASSOCIATION;
CHINESE HAN POPULATION;
ALLERGIC-ASTHMA;
CHILDHOOD ASTHMA;
AIRWAY HYPERRESPONSIVENESS;
SUSCEPTIBILITY GENES;
MAMMALIAN CHITINASE;
D O I:
10.1186/1465-9921-12-86
中图分类号:
R56 [呼吸系及胸部疾病];
学科分类号:
摘要:
Background: Little is known about the role of most asthma susceptibility genes during human lung development. Genetic determinants for normal lung development are not only important early in life, but also for later lung function. Objective: To investigate the role of expression patterns of well-defined asthma susceptibility genes during human and murine lung development. We hypothesized that genes influencing normal airways development would be over-represented by genes associated with asthma. Methods: Asthma genes were first identified via comprehensive search of the current literature. Next, we analyzed their expression patterns in the developing human lung during the pseudoglandular (gestational age, 7-16 weeks) and canalicular (17-26 weeks) stages of development, and in the complete developing lung time series of 3 mouse strains: A/J, SW, C57BL6. Results: In total, 96 genes with association to asthma in at least two human populations were identified in the literature. Overall, there was no significant over-representation of the asthma genes among genes differentially expressed during lung development, although trends were seen in the human (Odds ratio, OR 1.22, confidence interval, CI 0.90-1.62) and C57BL6 mouse (OR 1.41, CI 0.92-2.11) data. However, differential expression of some asthma genes was consistent in both developing human and murine lung, e.g. NOD1, EDN1, CCL5, RORA and HLAG. Among the asthma genes identified in genome wide association studies, ROBO1, RORA, HLA-DQB1, IL2RB and PDE10A were differentially expressed during human lung development. Conclusions: Our data provide insight about the role of asthma susceptibility genes during lung development and suggest common mechanisms underlying lung morphogenesis and pathogenesis of respiratory diseases.
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