Title | Parasympathetic innervation regulates tubulogenesis in the developing salivary gland. |
Publication Type | Journal Article |
Year of Publication | 2014 |
Authors | Nedvetsky PI, Emmerson E, Finley JK, Ettinger A, Cruz-Pacheco N, Prochazka J, Haddox CL, Northrup E, Hodges C, Mostov KE, Hoffman MP, Knox SM |
Journal | Dev Cell |
Volume | 30 |
Issue | 4 |
Pagination | 449-62 |
Date Published | 2014 Aug 25 |
ISSN | 1878-1551 |
Keywords | Animals, Apoptosis, Cyclic AMP, Cyclic AMP-Dependent Protein Kinases, Cystic Fibrosis Transmembrane Conductance Regulator, Epithelial Cells, Ganglia, Parasympathetic, Mice, Mice, Inbred ICR, Organogenesis, Salivary Ducts, Vasoactive Intestinal Peptide |
Abstract | A fundamental question in development is how cells assemble to form a tubular network during organ formation. In glandular organs, tubulogenesis is a multistep process requiring coordinated proliferation, polarization and reorganization of epithelial cells to form a lumen, and lumen expansion. Although it is clear that epithelial cells possess an intrinsic ability to organize into polarized structures, the mechanisms coordinating morphogenetic processes during tubulogenesis are poorly understood. Here, we demonstrate that parasympathetic nerves regulate tubulogenesis in the developing salivary gland. We show that vasoactive intestinal peptide (VIP) secreted by the innervating ganglia promotes ductal growth, leads to the formation of a contiguous lumen, and facilitates lumen expansion through a cyclic AMP/protein kinase A (cAMP/PKA)-dependent pathway. Furthermore, we provide evidence that lumen expansion is independent of apoptosis and involves the cystic fibrosis transmembrane conductance regulator (CFTR), a cAMP-regulated Cl(-) channel. Thus, parasympathetic innervation coordinates multiple steps in tubulogenesis during organogenesis. |
DOI | 10.1016/j.devcel.2014.06.012 |
Alternate Journal | Dev. Cell |
PubMed ID | 25158854 |
PubMed Central ID | PMC4155578 |
Grant List | S10 RR26758 / RR / NCRR NIH HHS / United States 5R01DK091530 / DK / NIDDK NIH HHS / United States S10 RR026758 / RR / NCRR NIH HHS / United States R21 DE022951 / DE / NIDCR NIH HHS / United States R00 DE018969 / DE / NIDCR NIH HHS / United States 5R00DE018969 / DE / NIDCR NIH HHS / United States R01 DK091530 / DK / NIDDK NIH HHS / United States 5R01DK074398 / DK / NIDDK NIH HHS / United States R21DE022951 / DE / NIDCR NIH HHS / United States R01 DK074398 / DK / NIDDK NIH HHS / United States |