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Gestational Exposure to Sidestream (Secondhand) Cigarette Smoke Promotes Transgenerational Epigenetic Transmission of Exacerbated Allergic Asthma and Bronchopulmonary Dysplasia.
- Source :
-
Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 2017 May 15; Vol. 198 (10), pp. 3815-3822. Date of Electronic Publication: 2017 Apr 05. - Publication Year :
- 2017
-
Abstract
- Embryonic development is highly sensitive to xenobiotic toxicity and in utero exposure to environmental toxins affects physiological responses of the progeny. In the United States, the prevalence of allergic asthma (AA) is inexplicably rising and in utero exposure to cigarette smoke increases the risk of AA and bronchopulmonary dysplasia (BPD) in children and animal models. We reported that gestational exposure to sidestream cigarette smoke (SS), or secondhand smoke, promoted nicotinic acetylcholine receptor-dependent exacerbation of AA and BPD in mice. Recently, perinatal nicotine injections in rats were reported to induce peroxisome proliferator-activated receptor γ-dependent transgenerational transmission of asthma. Herein, we show that first generation and second generation progeny from gestationally SS-exposed mice exhibit exacerbated AA and BPD that is not dependent on the decrease in peroxisome proliferator-activated receptor γ levels. Lungs from these mice show strong eosinophilic infiltration, excessive Th2 polarization, marked airway hyperresponsiveness, alveolar simplification, decreased lung compliance, and decreased lung angiogenesis. At the molecular level, these changes are associated with increased RUNX3 expression, alveolar cell apoptosis, and the antiangiogenic factor GAX, and decreased expression of HIF-1α and proangiogenic factors NF-κB and VEGFR2 in the 7-d first generation and second generation lungs. Moreover, the lungs from these mice exhibit lower levels of microRNA (miR)-130a and increased levels of miR-16 and miR-221. These miRs regulate HIF-1α-regulated apoptotic, angiogenic, and immune pathways. Thus the intergenerational effects of gestational SS involve epigenetic regulation of HIF-1α through specific miRs contributing to increased incidence of AA and BPD in the progenies.<br /> (Copyright © 2017 by The American Association of Immunologists, Inc.)
- Subjects :
- Alveolar Epithelial Cells pathology
Animals
Apoptosis
Asthma immunology
Asthma physiopathology
Bronchopulmonary Dysplasia immunology
Bronchopulmonary Dysplasia physiopathology
Core Binding Factor Alpha 3 Subunit genetics
Female
Homeodomain Proteins genetics
Hypoxia-Inducible Factor 1, alpha Subunit genetics
Lung pathology
Mice
MicroRNAs genetics
NF-kappa B p50 Subunit genetics
Nerve Growth Factors
Neuropeptides genetics
Nicotine adverse effects
PPAR gamma genetics
PPAR gamma metabolism
Pregnancy
Prenatal Exposure Delayed Effects physiopathology
Smoking adverse effects
Th2 Cells immunology
Asthma etiology
Asthma genetics
Bronchopulmonary Dysplasia etiology
Epigenesis, Genetic
Prenatal Exposure Delayed Effects immunology
Smoke adverse effects
Tobacco Smoke Pollution adverse effects
Subjects
Details
- Language :
- English
- ISSN :
- 1550-6606
- Volume :
- 198
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Journal of immunology (Baltimore, Md. : 1950)
- Publication Type :
- Academic Journal
- Accession number :
- 28381639
- Full Text :
- https://doi.org/10.4049/jimmunol.1700014