Maternal Exposure to PM2.5 Affects Fetal Lung Development at Sensitive Windows

Lung development continues from the embryonic period to adulthood. Previous epidemiological studies have noted that maternal exposure of atmospheric pollutants during the sensitive windows disturbed the lung development and increased the risk of lung diseases after birth, but the experimental evidence was insufficient. In the present study, we exposed plug-positive mice to PM 2.5 (3 mg/kg b.w.) by oropharyngeal aspiration every other day, and intended to test whether maternal PM 2.5 exposure affected prenatal lung development in the offspring. First, maternal PM 2.5 exposure decreased embryo weight and crown-rump length at E18.5 but not in earlier developmental stages (E0–E16.5). Second, maternal PM 2.5 exposure did not prevent lung-bud and tracheal specification, and did not cause abnormalities in branching morphogenesis, distal lung epithelium, and mesenchyme differentiation in earlier stages of lung development (E0–E16.5). However, the exposure significantly disturbed the distal lung epithelium and mesenchyme differentiation of lung, led to reduced intact rings of trachea, and suppressed the expression of lung development-related genes ( Nkx2.1, Tbx4, Tbx5, and Sox9 ) at E18.5. Finally, we found that the exposure not only increased PM 2.5 -bound metal content (Pb and Cu) but also caused inflammatory response in the placenta, which transmitted from the mother to the fetus and contributed to the developmental abnormalities.