Time series of transcriptome analysis in entire lung development stages provide insights into the origin of NO2 related lung diseases
Nkx2.5 participated in abnormal lung muscle development induced by maternal NO2 exposure. [Display omitted] •Maternal NO2 exposure induce time-series changes in lung genome expression profile.•Maternal NO2 exposure disturb lung vein myocardium development in fetus/offspring.•Nkx2.5 may be related to...
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Veröffentlicht in: | Environment international 2022-10, Vol.168, p.107454-107454, Article 107454 |
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Zusammenfassung: | Nkx2.5 participated in abnormal lung muscle development induced by maternal NO2 exposure.
[Display omitted]
•Maternal NO2 exposure induce time-series changes in lung genome expression profile.•Maternal NO2 exposure disturb lung vein myocardium development in fetus/offspring.•Nkx2.5 may be related to abnormal lung development induced by maternal NO2 exposure.
Lung growth is a critical window, when exposure to various pollutants can disturb the finely-tuned lung development and enhance risk of long-term structural and functional sequelae of lung. In this study, pregnant C57/6 mice were treated with NO2, and lungs of fetus/offspring were collected at different developmental windows and dynamic lung development was determined. The results showed that maternal NO2 exposure suppressed fetal weight, implying that fetal development can be disturbed. The time-series RNA-seq analysis of lungs showed that maternal NO2 exposure induced significant time-dependent changes in the expression profiles of genes associated with lung vein myocardium development in fetus/offspring. Most of these genes in NO2 exposure group were suppressed at middle gestation and at birth. Our results also indicated that the gene expressions of Nkx2.5 in NO2 exposure were suppressed to 0.27- and 0.44-fold of the corresponding Air group at E13.5 and PND1, and restored at later time points. This indicated that the transcription factor Nkx2.5 played an important role in abnormal lung development in fetus/offspring caused by maternal NO2 exposure. Importantly, gene expressions of lung vein myocardium development were related to transcription factors (TFs) and lung functions, and TFs showed similar trends with lung function. These results provide a comprehensive view of the adverse effects of maternal NO2 exposure on fetal lung development by uncovering molecular targets and related signaling pathways at the transcriptional level. |
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ISSN: | 0160-4120 1873-6750 |
DOI: | 10.1016/j.envint.2022.107454 |