| First Author | Liu J | Year | 2019 |
| Journal | Am J Physiol Lung Cell Mol Physiol | Volume | 317 |
| Issue | 2 | Pages | L202-L211 |
| PubMed ID | 31042081 | Mgi Jnum | J:277670 |
| Mgi Id | MGI:6331197 | Doi | 10.1152/ajplung.00295.2018 |
| Citation | Liu J, et al. (2019) (Pro)renin receptor regulates lung development via the Wnt/beta-catenin signaling pathway. Am J Physiol Lung Cell Mol Physiol 317(2):L202-L211 |
| abstractText | The (pro)renin receptor [(P)RR] binds to prorenin to activate the renin-angiotensin system and is essential for the development of many different organ systems. Whether the (P)RR also plays a role in lung development is unknown. Immunostaining was used to determine the spatial-temporal distribution of (P)RR in the embryonic, postnatal, and adult lungs. We created a lung-specific (P)RR knockout mouse [Foxd1(cre/+)-(P)RR(flox/flox)] and assessed changes in lung morphology, cell proliferation, and apoptosis using immunohistochemistry and TUNEL staining. (P)RR function was confirmed by using siRNA to knock down (P)RR in human bronchial epithelial cells (HBECs) and then using the CCK-8 assay and flow cytometry to assess cell proliferation and apoptosis. Gene expression changes after knockdown were assessed by RT-PCR and Western blotting. (P)RR is expressed in the club cells of the bronchial epithelium, and expression increases throughout development. Lung-specific (P)RR knockout disrupted branching morphogenesis, leading to lung hypoplasia and neonatal mortality. These defects were associated with increased apoptosis and decreased proliferation of the pulmonary epithelial and mesenchymal cells and may be mediated by downregulation of Wnt11, beta-catenin, and Axin2. (P)RR regulates lung development through canonical Wnt/beta-catenin signaling and may present a new target for strategies to treat lung hypoplasia. |
