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Publication : IKKβ Activation in the Fetal Lung Mesenchyme Alters Lung Vascular Development but Not Airway Morphogenesis.

First Author  McCoy AM Year  2017
Journal  Am J Pathol Volume  187
Issue  12 Pages  2635-2644
PubMed ID  28923684 Mgi Jnum  J:252121
Mgi Id  MGI:6094724 Doi  10.1016/j.ajpath.2017.08.013
Citation  McCoy AM, et al. (2017) IKKbeta Activation in the Fetal Lung Mesenchyme Alters Lung Vascular Development but Not Airway Morphogenesis. Am J Pathol 187(12):2635-2644
abstractText  In the immature lung, inflammation and injury disrupt the epithelial-mesenchymal interactions required for normal development. Innate immune signaling and NF-kappaB activation disrupt the normal expression of multiple mesenchymal genes that play a key role in airway branching and alveolar formation. To test the role of the NF-kappaB pathway specifically in lung mesenchyme, we utilized the mesenchymal Twist2-Cre to drive expression of a constitutively active inhibitor of NF-kappaB kinase subunit beta (IKKbetaca) mutant in developing mice. Embryonic Twist2-IKKbetaca mice were generated in expected numbers and appeared grossly normal. Airway branching also appeared normal in Twist2-IKKbetaca embryos, with airway morphometry, elastin staining, and saccular branching similar to those in control littermates. While Twist2-IKKbetaca lungs did not contain increased levels of Il1b, we did measure an increased expression of the chemokine-encoding gene Ccl2. Twist2-IKKbetaca lungs had increased staining for the vascular marker platelet endothelial cell adhesion molecule 1. In addition, type I alveolar epithelial differentiation appeared to be diminished in Twist2-IKKbetaca lungs. The normal airway branching and lack of Il1b expression may have been due to the inability of the Twist2-IKKbetaca transgene to induce inflammasome activity. While Twist2-IKKbetaca lungs had an increased number of macrophages, inflammasome expression remained restricted to macrophages without evidence of spontaneous inflammasome activity. These results emphasize the importance of cellular niche in considering how inflammatory signaling influences fetal lung development.
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