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. Author manuscript; available in PMC: 2016 Mar 1.
Published in final edited form as: J Pediatr. 2014 Nov 6;166(3):531–537.e13. doi: 10.1016/j.jpeds.2014.09.052

Figure 2.

Figure 2

Evaluation of miR-219 and CD44 in a newborn mouse model (Panels A-D) and in human lung (Panels E-F). Lung miR-219 (Panel A) and CD44 mRNA (Panel B) decreased during alveolar septation, with expression on postnatal days 14 and 42 significantly less as compared with day 1; *p<0.05. Lung miR-219 (Panel C) and CD44 mRNA (Panel D) were also increased on postnatal day 14 during hyperoxia exposure (*p<0.05 compared with air). Lung miR-219 (Panel E) and CD44 mRNA (Panel F) were increased in human lungs with BPD as compared to early preterm or term stillbirth lungs (Mean±SEM; n=4/group)